Highlights
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A systemic review of T cell epitopes of SARS-CoV-2 proteome.
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The HLA restriction of defined T cell epitopes of SARS-CoV-2.
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The methods identifying the T cell epitopes of SARS-CoV-2.
Keywords: SARS-CoV-2, T-cell epitope, HLA restriction
Abstract
Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection remains in a global pandemic, and no eradicative therapy is currently available. Host T cells have been shown to play a crucial role in the antiviral immune protection and pathology in Coronavirus disease 2019 (COVID-19) patients; thus, identifying sufficient T-cell epitopes from the SARS-CoV-2 proteome can contribute greatly to the development of T-cell epitope vaccines and the precise evaluation of host SARS-CoV-2-specific cellular immunity. This review presents a comprehensive map of T-cell epitopes functionally validated from SARS-CoV-2 antigens, the human leukocyte antigen (HLA) supertypes to present these epitopes, and the strategies to screen and identify T-cell epitopes. To the best of our knowledge, a total of 1349 CD8+ T-cell epitopes and 790 CD4+ T-cell epitopes have been defined by functional experiments thus far, but most are presented by approximately twenty common HLA supertypes, such as HLA-A0201, A2402, B0702, DR15, DR7 and DR11 molecules, and 74-80% of the T-cell epitopes are derived from S protein and nonstructural protein. These data provide useful insight into the development of vaccines and specific T-cell detection systems. However, the currently defined T-cell epitope repertoire cannot cover the HLA polymorphism of major populations in an indicated geographic region. More research is needed to depict an overall landscape of T-cell epitopes, which covers the overall SARS-CoV-2 proteome and global patients.
1. Introduction
The SARS-CoV-2 infection remains in a large-scale epidemic. As of October 12, 2022, there were over 619.8 million cases diagnosed and over 6.5 million deaths worldwide due to this disease. Numerous studies have shown that SARS-CoV-2-specific T-cell responses have important effects on viral clearance (Yu et al., 2020), disease progression (Rydyznski Moderbacher et al., 2020), antiviral efficacy (Oberhardt et al., 2021) and superinfection (Zuo et al., 2021), especially CD8+ T cells, which are important effector cells that kill virus-infected cells and secrete cytokines. Therefore, specific T cells against SARS-CoV-2 are not only potential markers to monitor the efficacy of antiviral therapy and predict the possibility of reinfection (Toor et al., 2021) but also potential specific immune modulators (Caccamo et al., 2020). Identifying as many T-cell epitopes as possible from SARS-CoV-2 antigens is of great significance for designing and developing epitope-peptide-based T-cell therapeutics and detecting host SARS-CoV-2-specific T-cell immunity.
This review systematically collected the CD8+ T-cell epitopes and CD4+ T-cell epitopes functionally defined from the SARS-CoV-2 proteome. The information is based on English-language journal papers indexed in databases such as PubMed, Scopus, Embase, SinoMed, and Google Scholar. The latest online search was conducted on August 15, 2022. “T-cell epitope” and “SARS-CoV-2” were used as specific search terms. An initial search identified 367 studies from multiple databases and manual searches. All articles were imported into Endnote software 20 (Thompson and Reuters, Philadelphia, PA, USA), and 60 duplicates were removed. In total, 307 studies from 2019 to 2022 were collected. Then, 237 articles were filtered out after abstract and full-text screening, according to the following exclusion criteria: (1) not related to the screening or identification of T-cell epitopes; (2) using only in silico prediction or molecular structure bioinformatic analysis rather than cell functional experiments, tetramer staining, binding assay, stabilization assay, or immunization; and (3) incomplete information regarding epitope sequences. Finally, 70 articles were used and referenced in this review.
2. Relation of HLA allele polymorphisms with SARS-CoV-2 infection
Human leukocyte antigen (HLA) class I molecules (classical HLA-A, HLA-B and HLA-C) expressed by virus-infected cells present viral endogenous epitope peptides to specific CD8+ T cells, thereby initiating the activation, proliferation and differentiation of naive T cells into cytotoxic T lymphocytes (CTLs). Then, virus-specific CTLs induce cytolysis of virus-infected cells through the Fas/FasL, TNF/TNFL and perforin/granzyme pathways (Nitschke et al., 2016). HLA class II molecules (classical HLA-DR, -DQ and -DP) on antigen-presenting cells (APCs, such as monocytes, macrophages, dendritic cells, and B cells) present exogenous viral polypeptides to CD4+ helper T cells, thereby inducing naive CD4+ T cells to differentiate into efficient Th1 or Th2 cells. The former mechanism helps the activation of virus-specific CD8+ T cells, and the latter mechanism assists virus-specific B cells in producing antibodies (Roche and Furuta, 2015). However, HLA molecules are highly polymorphic in the general population. According to information provided by the International Immunogenetics Information Project/HLA database (IMGT; https://www.ebi.ac.uk/ipd/imgt/hla/), as of July 2022, a total of 35077 alleles were found at HLA class I and class II gene loci in the global population, including 7562 HLA-A, 9000 HLA-B, 7513 HLA-C, 4149 HLA-DRB, 2278 HLA-DQB1, and 2067 HLA-DPB1. HLA genotypes vary from person to person, and the antigenic epitope peptides presented by different HLA allotypes are also distinct. Therefore, the immune patterns of different individuals to the same pathogen show large diversity (Elahi and Horton, 2012; Wang et al., 2016). Furthermore, there are significant differences in the distribution of HLA alleles in different ethnic populations and geographic regions (http://www.allelefrequencies.net).
An increasing number of studies have revealed the correlation between HLA allotypes and the occurrence of certain diseases (Boeijen et al., 2017; Medzhitov, 2007). Although the association of HLA alleles with SARS-CoV-2 infection is not fully understood, this relationship continues to be revealed by past and present studies. In a study of the Italian Sardinian population, the 4 alleles (HLA-A*02:05, B*58:01, C*07:01, DRB1*03:01) played a positive role in the protection of host against SARS-CoV-2 infection. The presence of the HLA-DRB1*08:01 allele has an adverse effect on the disease progression of COVID-19 patients (Littera et al., 2020). A study in a Caucasian population in the United States showed that HLA-B*15:01 was closely associated with asymptomatic infection with SARS-CoV-2 (Augusto et al., 2021). A study conducted in Zhejiang Province found that HLA-A*11:01, B*51:01 and C*14:02 alleles were associated with poor prognosis in SARS-CoV-2 infection (Wang et al., 2020). In the past two years, a large number of studies on the correlation between SARS-CoV-2 infection and HLA alleles have emerged, but some results seem to be inconsistent, which can be attributed to the polymorphism of host HLAs in different races and regions (Matern et al., 2020; Zidi et al., 2016). Therefore, further studies should be conducted in different regions to reduce the heterogeneity.
3. SARS-CoV-2 proteins
The genome of SARS-CoV-2 is a positive single-stranded RNA with a length of 29.9kb. Proteins translated from the SARS-CoV-2 genome are classified into three main groups: nonstructural proteins, structural proteins, and accessory proteins. The ORF sequences of nonstructural proteins are located upstream of the genome encoding pp1a and pp1ab, and the ORF sequences of structural and accessory proteins are located downstream of the genome. The structural protein coding region mainly encodes the spike (S) protein, envelope (E) protein, membrane (M) protein and nucleocapsid (N) protein. The accessory proteins included ORF3a, ORF3b, ORF6, ORF7a, ORF7b, ORF8, ORF9b, ORF9c and ORF10.
The binding of the S protein to host cells via its receptor binding domain (RBD) plays an important role in pathogenesis, since it initiates infection by attaching viral particles to host cells. The S protein consists of 1273 amino acid residues, including three subunits, namely, S1, S2 and S2′, which play different roles in the process of adhesion to host cells. By interacting with human angiotensin-converting enzyme 2 (ACE2), the S1 subunit is involved in the attachment of virions to the host cell membrane and subsequently initiates the infection process (Lan et al., 2020). The S2 subunit functions as a fusion protein that facilitates the fusion of the virion with the cell membrane (Naqvi et al., 2020). The relatively smaller E protein (75 amino acids) plays an important role in viral morphogenesis and assembly, and acts as a viral pore protein that is assembled into the host cell membrane to form protein-lipid pores for ion transport. The M protein, with a length of 222 amino acids, plays a role together with the E, N and S proteins in the process of virus infection of the body, and plays a major role in the assembly process of viral RNA (Tang et al., 2020). The M protein is the most abundant viral protein in coronaviruses and is involved in the composition of different shapes of the virus. The N protein performs viral assembly by interacting with the viral genome and M protein. This protein binds to viral RNA in a "beaded" manner through an RNA-binding domain of approximately 140 amino acids in its core (Li et al., 2020), helping to enhance viral RNA transcription and replication (Cong et al., 2020).
4. Strategies for screening T-cell epitopes
The first step in screening T-cell epitopes is selecting the candidate epitope peptides. Generally, two strategies have been used. One is to generate an overlapping peptides (OLP) library that spans the entire proteome or indicated proteins (peptide scanning) (Zelba et al., 2021). Another strategy is to use predicted epitope peptides that bind to indicated HLA allotypes as predicted in silico through a variety of epitope prediction tools and algorithms (Grifoni et al., 2020). Epitope prediction tools can also be used to assess the HLA restriction of epitope peptides defined by cellular experiments. In a recent study, the researchers used the NetMHCpan Version EL4.1 algorithm in the IEDB database to evaluate the binding ability of the reported epitope peptides to MHC-I molecules in order to screen out those with stronger binding ability, and a predominant epitope peptide was used to immunize mice with an epitope peptide vaccine (Jiang et al., 2022).
Over the past two decades, methods for verifying the immunogenicity of candidate epitope peptides have undergone numerous improvements. Currently, widely used methods include: cytotoxicity assays, lymphocyte proliferation assays, intracellular cytokine staining (ICS), enzyme-linked immunospot assays (ELISpot)/fluorescence immunospot assays (FluorSpot), activation-induced marker assays (AIM) and polypeptide-MHC multimer staining. The cytotoxicity assay validated CD8+ T-cell epitopes by stimulating PBMCs with candidate epitope peptides and coculturing them with Cr51-labeled target cells (Shafer-Weaver et al., 2003). At present, the more common methods used are ICS, AIM and ELISpot/FluorSpot. PBMCs from patients were stimulated in vivo or in vitro with candidate epitope peptides, followed by the detection of cytokines secreted by CD4+ T cells or CD8+ T cells or markers on activated T cells (Freer and Rindi, 2013). ELISpot or FluorSpot technology can detect single activated cells in one million PBMCs. Because of its accuracy, sensitivity, and repeatability, the technology has been widely used in research and has promising clinical prospects for detecting antigen-specific T cells (Ji and Forsthuber, 2016; Portilho et al., 2022). Peptide-HLA multimer staining has become the gold standard for enumeration of antigen-specific T cells because of its high specificity and also has been used to identify T-cell epitopes in many studies. Yuri et al. used peptide-HLA multimer staining to verify the SARS-CoV-2 epitope peptides predicted by the IEDB database, and defined 31 CD8+ T-cell epitopes and 19 CD4+ T-cell epitopes (Poluektov et al., 2021). Many researchers have also established HLA transgenic mouse models to map HLA-restricted epitopes. Lauren et al. predicted 32 SARS-CoV-2-specific T-cell epitope peptides by the EpiMatrix algorithm and selected 20 peptides to generate epitope peptide vaccines followed by immunization of HLA-DR3 transgenic mice for the evaluation of protective effects (Meyers et al., 2021). Peptide-HLA molecule binding and stability assays are also used to identify antigenic epitopes. More recently, a high-throughput genome-wide screening by identifying target cells expressing T-cell epitopes recognized by T cells (T-Scan) was used to define T-cell epitopes of SARS-CoV-2 (Zhang et al., 2021).
5. Identified SARS-CoV-2 antigen-specific T-cell epitopes
Tables 1 and 2 present the CD8+ T-cell epitopes and CD4+ T-cell epitopes identified from SARS-CoV-2 proteins, respectively, and display the HLA restriction of these eptiopes and the methods validating the immunogenicity of these peptides. The CD8+ T-cell epitopes collected in this review are 8-15 amino acids in length; the CD4+ T-cell epitopes are 10-20 amino acids in length. Epitope peptides with the lengths that are too long or too short easily produce false-positive results in validation experiments (Paul et al., 2020), so they are excluded from this review.
Table 1.
List of CD8+ T-cell epitopes validated from SARS-CoV-2 antigens.
| Sequence | Protein | Start | End | HLA restriction | Methods to validate the epitope peptides | References |
|---|---|---|---|---|---|---|
| AADLDDFSKQL | N | 397 | 407 | A*02:01 | multimer staining | (Saini et al., 2021) |
| AEGSRGGSQA | N | 173 | 182 | HLA class I | HTMA | (Snyder et al., 2020) |
| AGLPYGANK | N | 119 | 127 | A*30:01 | AIM | (Tarke et al., 2021) |
| ALALLLLDRL | N | 218 | 227 | A2 | ELISPOT | (Lee et al., 2021) |
| ALNTPKDHI | N | 138 | 146 | A*02:01 | ICS | (Szeto et al., 2021) |
| APRITFGGP | N | 12 | 20 | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| APSASAFFGM | N | 308 | 317 | B*07:02 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| AQFAPSASA | N | 305 | 313 | B*15:01/A*02:01 | ICS | (Wagner et al., 2022; Habel et al., 2020) |
| AQFAPSASAF | N | 305 | 314 | B*15:01/A*24:02 | ICS/ELISA/multimer staining | (Saini et al., 2021; Titov et al., 2022; Schulien et al., 2021; Swaminathan et al., 2022) |
| AQFAPSASAFFGMSR | N | 305 | 319 | HLA class I | HTMA | (Snyder et al., 2020) |
| ASAFFGMSR | N | 311 | 319 | A*68:01/A*11:01 | AIM/ELISA/cytotoxicity | (Tarke et al., 2021; Ferretti et al., 2020) |
| ATEGALNTPK | N | 134 | 143 | A*11:01 | AIM/ELISA/cytotoxicity/ICS/ELISPOT | (Tarke et al., 2021; Wagner et al., 2022; Titov et al., 2022; Swaminathan et al., 2022; Ferretti et al., 2020; Nelde et al., 2021) |
| ATEGALNTPKDHI | N | 134 | 146 | HLA class I | HTMA | (Snyder et al., 2020) |
| AYKTFPPTEPK | N | 359 | 369 | HLA class I | HTMA | (Snyder et al., 2020) |
| DLSPRWYFYY | N | 103 | 112 | A2/A29 | ELISPOT | (Schmidt et al., 2021) |
| DLSPRWYFYYL | N | 103 | 113 | A2/A29 | ELISPOT | (Schmidt et al., 2021) |
| DLSPRWYFYYLGTGP | N | 103 | 117 | HLA class I | ICS/AIM | (Schmidt et al., 2021) |
| DYKHWPQIAQF | N | 297 | 307 | A*24:02 | ELISPOT/ICS | (Nelde et al., 2021) |
| ELIRQGTDY | N | 290 | 298 | A*26:01 | AIM | (Tarke et al., 2021) |
| EVTPSGTWLTY | N | 323 | 333 | A*26:01 | AIM | (Tarke et al., 2021) |
| FAPSASAFF | N | 307 | 315 | B*35:01 | ELISPOT/AIM | (Tarke et al., 2021; Somogyi et al., 2021) |
| FPRGQGVPI | N | 66 | 74 | B*07:02/B*08:01 | ICS/AIM/multimer staining/ELISPOT | (Saini et al., 2021; Tarke et al., 2021; Schulien et al., 2021; Swaminathan et al., 2022; Nelde et al., 2021) |
| FSKQLQQSM | N | 403 | 411 | HLA class I | ELISPOT/HTMA | (Snyder et al., 2020; Somogyi et al., 2021) |
| GMEVTPSGTWLTY | N | 321 | 333 | HLA class I | HTMA | (Snyder et al., 2020) |
| GMEVTPSGTWLTYTG | N | 321 | 335 | HLA class I | AIM/ELISPOT | (Zhao et al., 2021) |
| GMSRIGMEV | N | 316 | 324 | A*02:01 | ICS/AIM/ELISPOT/multimer staining | (Saini et al., 2021; Tarke et al., 2021; Szeto et al., 2021; Habel et al., 2020; Schulien et al., 2021; Hu et al., 2022) |
| GMSRIGMEVTPSGTW | N | 316 | 330 | HLA class I | HTMA | (Snyder et al., 2020) |
| GPQNQRNAPRITF | N | 5 | 17 | B*07:02 | AIM | (Tarke et al., 2021) |
| GTGPEAGLPY | N | 114 | 123 | HLA class I | HTMA | (Snyder et al., 2020) |
| GTRNPANNA | N | 147 | 155 | A*30:01 | AIM | (Tarke et al., 2021) |
| HWPQIAQF | N | 300 | 307 | A*24:02 | multimer staining | (Saini et al., 2021) |
| IGYYRRATR | N | 84 | 92 | A*33:03 | ICS | (Jin et al., 2021) |
| IIWVATEGA | N | 130 | 138 | A*02:01 | ICS/AIM | (Lee et al., 2021) |
| IKLDDKDPNFKDQVI | N | 337 | 351 | HLA class I | AIM | (Zhao et al., 2021) |
| ILLNKHID | N | 351 | 358 | A*02:01 | ICS | (Szeto et al., 2021) |
| ILLNKHIDA | N | 351 | 359 | A*02:01 | HTMA/ICS | (Snyder et al., 2020; Szeto et al., 2021) |
| KAYNVTQAF | N | 266 | 274 | B*35:01/B*57:01/B*51:01 | ELISPOT/AIM/ELISA/HTMA | (Snyder et al., 2020; Tarke et al., 2021; Titov et al., 2022; Somogyi et al., 2021) |
| KFPRGQGVPI | N | 65 | 74 | HLA class I | HTMA | (Snyder et al., 2020) |
| KIFPPTEPK | N | 361 | 369 | A*11:01 | ELISA | (Hu et al., 2022) |
| KKQQTVTLL | N | 387 | 395 | C*07:01 | multimer staining | (Saini et al., 2021) |
| KLDDKDPNF | N | 338 | 346 | A*02:01 | ELISPOT/multimer staining | (Hu et al., 2022; Poran et al., 2020) |
| KMKDLSPRW | N | 100 | 108 | B*57:01 | AIM/HTMA | (Snyder et al., 2020; Tarke et al., 2021) |
| KPRQKRTAT | N | 257 | 265 | B*07:02/B*08:01 | ICS/AIM/ multimer staining | (Saini et al., 2021; Tarke et al., 2021; Schulien et al., 2021; Swaminathan et al., 2022; Panikkar et al., 2022) |
| KSAAEASKK | N | 249 | 257 | A*11:01 | AIM | (Tarke et al., 2021) |
| KTFPPTEPK | N | 361 | 369 | A*03:01/A*11:01/A*68:01/A*30:01 | ICS/ELISPOT/multimer staining / AIM/ ELISA/cytotoxicity | (Saini et al., 2021; Tarke et al., 2021; Titov et al., 2022; Ferretti et al., 2020; Hu et al., 2022; Kared et al., 2021; Gangaev et al., 2021; Zhang et al., 2022; Peng et al., 2020; Zhang et al., 2022) |
| KTFPPTEPKK | N | 361 | 370 | A*11:01/A*03:01 | (Tarke et al., 2021; Wagner et al., 2022; Titov et al., 2022; Nelde et al., 2021) | |
| KTFPPTEPKKDKKK | N | 361 | 374 | A*03:01 | AIM | (Tarke et al., 2021) |
| KTLPPTEPK | N | 361 | 369 | A*11:01 | ELISA | (Hu et al., 2022) |
| LQLPQGTTL | N | 159 | 167 | A*02:01 | ICS | (Szeto et al., 2021) |
| LALLLLDRL | N | 219 | 227 | A*02:01/A*02:06 | ICS/ELISPOT | (Szeto et al., 2021; Schulien et al., 2021; Hu et al., 2022; Jin et al., 2021) |
| LLLDRLNQL | N | 222 | 230 | A*02:01 | ELISA/multimer staining/cytotoxicity/AIM/ICS/ELISPOT/proliferation | (Saini et al., 2021; Tarke et al., 2021; Szeto et al., 2021; Wagner et al., 2022; Titov et al., 2022; Schulien et al., 2021; Ferretti et al., 2020; Hu et al., 2022; Jin et al., 2021; Poran et al., 2020; Kared et al., 2021; Sekine et al., 2020; Quiros-Fernandez et al., 2021) |
| LLLLDRLNQL | N | 221 | 230 | A*02:01 | ELISA/multimer staining/ELISPOT/ICS | (Saini et al., 2021; Titov et al., 2022; Nelde et al., 2021) |
| LLNKHIDAY | N | 352 | 360 | B*15:01 | multimer staining | (Saini et al., 2021) |
| LPAADLDDF | N | 395 | 403 | B*35:01 | AIM/ELISA/HTMA | (Snyder et al., 2020; Tarke et al., 2021; Titov et al., 2022) |
| LPNNTASWF | N | 45 | 53 | B*07:02 | AIM/HTMA | (Snyder et al., 2020; Tarke et al., 2021) |
| LPYGANKDGI | N | 121 | 130 | B*51:01 | AIM | (Tarke et al., 2021) |
| LSPRWYFYY | N | 104 | 112 | A*24:02 | ICS | (Wagner et al., 2022) |
| LSPRWYFYYL | N | 104 | 113 | A*24:02 | HTMA/ICS | (Snyder et al., 2020; Jin et al., 2021) |
| MEVTPSGTW | N | 322 | 330 | B*44:03 | ICS/multimer staining/AIM/ELISA | (Titov et al., 2022; Schulien et al., 2021) |
| MEVTPSGTWL | N | 322 | 331 | B*40:01/B*40:10/B*44:10 | multimer staining/ELISPOT/ICS/AIM/ELISA | (Tarke et al., 2021; Wagner et al., 2022; Titov et al., 2022; Schulien et al., 2021; Swaminathan et al., 2022; Nelde et al., 2021; Panikkar et al., 2022; Peng et al., 2020; Agerer et al., 2021) |
| MKDLSPRWY | N | 101 | 109 | C*07:01 | multimer staining | (Saini et al., 2021) |
| MSDNGPQNQ | N | 1 | 9 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| MSRIGMEVTPSGTWL | N | 317 | 331 | HLA class I | ELISPOT | (Keller et al., 2020) |
| NQLESKMFG | N | 228 | 236 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| NPANNAAIVL | N | 150 | 159 | B*07:02 | AIM/ELISPOT | (Tarke et al., 2021; Nelde et al., 2021) |
| NSSPDDQIGYY | N | 77 | 87 | A*01:01 | multimer staining | (Nagler et al., 2021) |
| NTASWFTAL | N | 48 | 56 | A*02:06/A*02:01 | ELISPOT/proliferation/ICS | (Habel et al., 2020; Somogyi et al., 2021; Jin et al., 2021) |
| NTNSSPDDQIGYY | N | 75 | 87 | A*01:01 | AIM/HTMA/multimer staining | (Snyder et al., 2020; Tarke et al., 2021; Minervina et al., 2022) |
| NTPKDHIGTR | N | 140 | 149 | A*33:03 | ICS | (Jin et al., 2021) |
| NVTQAFGRR | N | 269 | 277 | A*33:03 | ICS | (Jin et al., 2021) |
| QLQQSMSSA | N | 406 | 414 | A*02:03 | ICS | (Jin et al., 2021) |
| QELIRQGTDY | N | 289 | 298 | B*44:02 | AIM/multimer staining | (Tarke et al., 2021; Minervina et al., 2022) |
| QELIRQGTDYKHW | N | 289 | 301 | HLA class I | HTMA | (Snyder et al., 2020) |
| QFAPSASAFF | N | 306 | 315 | A*24:02 | AIM | (Tarke et al., 2021) |
| QGLPNNTASW | N | 43 | 52 | B*57:01 | AIM | (Tarke et al., 2021) |
| QQQGQTVTK | N | 240 | 248 | A*11:01 | ELISA/proliferation | (Titov et al., 2022; Jin et al., 2021) |
| QQQQGQTVTK | N | 239 | 248 | HLA class I | HTMA | (Snyder et al., 2020) |
| QRNAPRITF | N | 9 | 17 | B*27:05/C*07:02/C*07:01 | multimer staining /ICS/ELISPOT | (Saini et al., 2021; Wagner et al., 2022; Swaminathan et al., 2022; Nelde et al., 2021; Peng et al., 2020) |
| QTVTLLPAA | N | 390 | 398 | A*02:06 | proliferation | (Jin et al., 2021) |
| QVILLNKHIDAYKTF | N | 349 | 363 | HLA class I | AIM | (Zhao et al., 2021) |
| RIRGGDGKM | N | 93 | 101 | B*07:02 | ICS/AIM | (Swaminathan et al., 2022; Panikkar et al., 2022) |
| RIRGGDGKMK | N | 93 | 102 | HLA class I | HTMA | (Snyder et al., 2020) |
| RLNQLESKM | N | 226 | 234 | A*02:01 | ICS | (Szeto et al., 2021) |
| RNPANNAAIVL | N | 149 | 159 | HLA class I | HTMA | (Snyder et al., 2020) |
| RPQGLPNNTA | N | 41 | 50 | B*07:02 | AIM | (Tarke et al., 2021) |
| RRGPEQTQGNF | N | 276 | 286 | C*07:01 | multimer staining | (Saini et al., 2021) |
| RTATKAYNV | N | 262 | 270 | A*02:01 | ICS/AIM | (Lee et al., 2021) |
| SASAFFGMSR | N | 310 | 319 | A*68:01 | AIM | (Tarke et al., 2021) |
| SPDDQIGYY | N | 79 | 87 | B*35:01 | AIM | (Tarke et al., 2021) |
| SPRWYFYYL | N | 29 | 37 | B*07:02/B*08:01/B*35 | ICS/multimer staining/AIM/ELISA/ELISPOT/cytotoxicity | (Saini et al., 2021; Tarke et al., 2021; Weingarten-Gabbay et al., 2021; Wagner et al., 2022; Titov et al., 2022; Schulien et al., 2021; Swaminathan et al., 2022; Ferretti et al., 2020; Schmidt et al., 2021; Panikkar et al., 2022; Kared et al., 2021; Peng et al., 2020; Sekine et al., 2020; Lineburg et al., 2021) |
| SQASSRSSSR | N | 180 | 189 | HLA class I | HTMA | (Snyder et al., 2020) |
| SSPDDQIGYY | N | 78 | 87 | C*04:01/B*35:01/B*35:02 | ELISA | (Titov et al., 2022) |
| SSPDDQIGYYR | N | 78 | 88 | A*01:01 | multimer staining | (Saini et al., 2021) |
| SSRGTSPAR | N | 201 | 209 | HLA class I | HTMA | (Snyder et al., 2020) |
| TPSGTWLTY | N | 325 | 333 | B*35:01 | AIM | (Tarke et al., 2021; Panikkar et al., 2022) |
| TPSGTWLTYTGAIKL | N | 325 | 339 | HLA class I | ELISPOT | (Zhao et al., 2021) |
| TPSGTWLTYTY | N | B*35:01 | ICS | (Swaminathan et al., 2022) | ||
| VLQLPQGTTL | N | 158 | 167 | A*02:01 | multimer staining | (Saini et al., 2021) |
| VTPSGTWLTY | N | 324 | 333 | A*30:02 | AIM | (Tarke et al., 2021) |
| WLTYTGAIKL | N | 330 | 339 | A*02:01 | ICS | (Jin et al., 2021) |
| YKTFPPTEPK | N | 360 | 369 | A*68:01/A*11:01 | AIM/ICS | (Tarke et al., 2021; Jin et al., 2021) |
| YLGTGPEAGL | N | 112 | 121 | A*02:01 | ICS/AIM/multimer staining | (Poran et al., 2020; Quiros-Fernandez et al., 2021) |
| YYRRATRRIR | N | 86 | 95 | HLA class I | HTMA | (Snyder et al., 2020) |
| FLAFVVFL | E | 20 | 27 | A*02:01 | multimer staining | (Poran et al., 2020) |
| FLAFVVFLL | E | 20 | 28 | A*02:01/A*02:07 | ELISPOT/proliferation/ICS | (Jin et al., 2021; Prakash et al., 2021) |
| FLAFVVFLLV | E | 20 | 29 | A*02:03 | ICS | (Jin et al., 2021) |
| FLLVTLAIL | E | 26 | 34 | A*02:01/A*02:07 | ELISPOT/multimer staining/ICS | (Jin et al., 2021; Prakash et al., 2021; Deng et al., 2021) |
| FYVYSRVKNL | E | 56 | 65 | A*24:02 | ELISPOT | (Nelde et al., 2021) |
| IVNSVLLFL | E | 13 | 21 | A*30:01 | proliferation/ICS | (Jin et al., 2021) |
| LFLAFVVFLL | E | 19 | 28 | A*02:07 | ICS | (Jin et al., 2021) |
| LIVNSVLLFL | E | 12 | 21 | A*02:06 | ICS | (Jin et al., 2021) |
| LVKPSFYVY | E | 51 | 59 | C*07:02 | multimer staining | (Saini et al., 2021) |
| NIVNVSLVK | E | 45 | 53 | A*11:01 | proliferation/ICS | (Jin et al., 2021) |
| RLCAYCCNIV | E | 38 | 47 | A*02:01 | ICS | (Jin et al., 2021) |
| RVKNLNSSR | E | 61 | 69 | A*30:01 | ICS | (Jin et al., 2021) |
| SEETGTLIV | E | 6 | 14 | HLA class I | HTMA | (Snyder et al., 2020) |
| SLVKPSFYV | E | 50 | 58 | HLA class I | HTMA | (Snyder et al., 2020) |
| SSRVPDLLV | E | 67 | 75 | A*30:01 | proliferation | (Jin et al., 2021) |
| SVLLFLAFV | E | 16 | 24 | A*02:07 | multimer staining/ICS | (Jin et al., 2021; Deng et al., 2021) |
| TLAILTALR | E | 30 | 38 | A*33:03 | proliferation | (Jin et al., 2021) |
| TLIVNSVLLF | E | 11 | 20 | A*24:02 | ICS | (Jin et al., 2021) |
| VFLLVTLAI | E | 25 | 33 | A*24:02 | ICS | (Jin et al., 2021) |
| VLLFLAFVV | E | 17 | 25 | A*02:01 | ICS | (Jin et al., 2021) |
| VLLFLAFVVF | E | 17 | 26 | A*24:02 | ICS | (Jin et al., 2021) |
| VNSVLLFLAF | E | 14 | 23 | A*24:02 | ICS | (Jin et al., 2021) |
| VSLVKPSFY | E | 49 | 57 | A*11:02 | ICS/proliferation | (Jin et al., 2021) |
| YVYSRVKN | E | 57 | 64 | HLA class I | ELISPOT | (Somogyi et al., 2021) |
| YVYSRVKNL | E | 57 | 65 | C*06:02 | HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020) |
| ANVYLKHGGGVAGAL | pp1a | 243 | 257 | HLA class I | ICS/AIM/intracellular staining | (Eggenhuizen et al., 2021) |
| LKHGGGVAGALNKAT | pp1a | 247 | 261 | HLA class I | ICS/AIM | (Eggenhuizen et al., 2021) |
| YLKHGGGVAGALNKA | pp1a | 246 | 260 | HLA class I | ICS/AIM/AIM | (Eggenhuizen et al., 2021) |
| AAISDYDYY | pp1ab | 4840 | 4848 | A*01:01 | multimer staining | (Saini et al., 2021) |
| AAISDYDYYR | pp1ab | 4840 | 4849 | A*68:01 | AIM | (Tarke et al., 2021) |
| AANFCALILA | pp1ab | 1707 | 1716 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| ADNFCALILA | pp1ab | 1707 | 1716 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| AEAELAKNV | pp1ab | 2616 | 2624 | B*44:02/B*44:03 | AIM | (Tarke et al., 2021) |
| AELAKNVSL | pp1ab | 2618 | 2626 | B*44:02 | AIM | (Tarke et al., 2021) |
| AELAKNVSLDNVL | pp1ab | 2618 | 2630 | HLA class I | HTMA | (Snyder et al., 2020) |
| AESHVDTDLTKPY | pp1ab | 4645 | 4657 | B*44:02 | AIM | (Tarke et al., 2021) |
| AEVAVKMF | pp1ab | 2584 | 2591 | B*44:02 | AIM | (Tarke et al., 2021) |
| AEWFLAYIL | pp1ab | 2325 | 2333 | B*40:01/B*44:02 | ICS/AIM | (Tarke et al., 2021; Schulien et al., 2021) |
| AEWFLAYILF | pp1ab | 2325 | 2334 | B*44:02 | AIM | (Tarke et al., 2021) |
| AGFSLWVYK | pp1ab | 6429 | 6437 | A*11:01 | multimer staining | (Kared et al., 2021) |
| AHAEETRKL | pp1ab | 1380 | 1388 | C*06:02 | multimer staining | (Saini et al., 2021) |
| AMRNAGIVGV | pp1ab | 4587 | 4596 | A*02:01 | ICS | (Jin et al., 2021) |
| AMYTPHTVL | pp1ab | 5315 | 5323 | A*32:01 | AIM | (Tarke et al., 2021) |
| APHGHVMVEL | pp1ab | 79 | 88 | B*07:02/A*02:01 | multimer staining | (Saini et al., 2021; Weingarten-Gabbay et al., 2021) |
| AIILASFSAST | pp1ab | 474 | 484 | HLA class I | HTMA | (Snyder et al., 2020) |
| AIMTRCLAV | pp1ab | 6199 | 6207 | HLA class I | HTMA | (Snyder et al., 2020) |
| AISDYDYYR | pp1ab | 4841 | 4849 | A*11:01 | AIM/proliferation | (Tarke et al., 2021; Jin et al., 2021) |
| AIVSTIQRK | pp1ab | 1397 | 1405 | A*03:01 | AIM | (Tarke et al., 2021) |
| AIVSTIQRKYK | pp1ab | 1397 | 1407 | A*03:01 | multimer staining | (Saini et al., 2021) |
| AKSHNIALIW | pp1ab | 2704 | 2713 | B*57:01 | AIM | (Tarke et al., 2021) |
| ALLADKFPV | pp1ab | 6245 | 6253 | A*02:01 | HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020) |
| ALRANSAVK | pp1ab | 4130 | 4138 | HLA class I | HTMA | (Snyder et al., 2020) |
| ALRKVPTDNY | pp1ab | 1316 | 1325 | B*15:01 | multimer staining | (Saini et al., 2021) |
| ALRKVPTDNYITTY | pp1ab | 1316 | 1329 | HLA class I | HTMA | (Snyder et al., 2020) |
| ALWEIQQV | pp1ab | 4094 | 4101 | A*02:01 | multimer staining | (Saini et al., 2021) |
| ALWEIQQVV | pp1ab | 4094 | 4102 | A*02:01 | ELISA/HTMA/multimer staining/cytotoxicity | (Saini et al., 2021; Snyder et al., 2020; Titov et al., 2022; Ferretti et al., 2020; Kared et al., 2021) |
| APKEIIFL | pp1ab | 735 | 742 | B*07:02 | multimer staining | (Saini et al., 2021) |
| APKEIIFLEGETL | pp1ab | 735 | 747 | HLA class I | HTMA | (Snyder et al., 2020) |
| APTLVPQEHYV | pp1ab | 5561 | 5571 | A*02:01 | multimer staining | (Saini et al., 2021) |
| APYIVGDVV | pp1ab | 1283 | 1291 | B*51:01 | AIM | (Tarke et al., 2021) |
| ARAGEAANF | pp1ab | 1702 | 1710 | C*07:01 | multimer staining | (Saini et al., 2021) |
| ARLYYDSMSY | pp1ab | 4904 | 4913 | C*07:02 | multimer staining | (Saini et al., 2021) |
| ASFDNFKFV | pp1ab | 1923 | 1931 | A*02:06/C*06:02 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| ASFNYLKSPNFSK | pp1ab | 2213 | 2225 | HLA class I | HTMA | (Snyder et al., 2020) |
| ASGNLLLDK | pp1ab | 4775 | 4783 | A*11:01 | proliferation | (Jin et al., 2021) |
| ASMPTTIAK | pp1ab | 2192 | 2200 | A*11:01/A*30:01/A*03:01 | ICS/AIM/ELISA/ELISPOT | (Tarke et al., 2021; Wagner et al., 2022; Titov et al., 2022; Schulien et al., 2021; Nelde et al., 2021) |
| ATVVIGTSK | pp1ab | 4977 | 4985 | A*11:01 | AIM/HTMA | (Snyder et al., 2020; Tarke et al., 2021) |
| AVAKHDFFK | pp1ab | 4487 | 4495 | A*11:01 | proliferation | (Jin et al., 2021) |
| AVASKILGL | pp1ab | 5844 | 5852 | A*02:01 | multimer staining | (Saini et al., 2021) |
| AVFDKNLYDK | pp1ab | 1176 | 1185 | A*11:01/A*03:01 | multimer staining | (Kared et al., 2021) |
| AVHFISNSW | pp1ab | 2355 | 2363 | B*57:01 | AIM | (Tarke et al., 2021) |
| AVLQSGFRK | pp1ab | 3260 | 3268 | HLA class I | HTMA | (Snyder et al., 2020) |
| AWPLIVTAL | pp1ab | 4123 | 4131 | A*24:02 | multimer staining | (Saini et al., 2021) |
| AYILFTRF | pp1ab | 2330 | 2337 | A*24:02 | AIM | (Tarke et al., 2021) |
| AYILFTRFF | pp1ab | 2330 | 2338 | A*24:02 | multimer staining | (Saini et al., 2021) |
| AYILFTRFFYV | pp1ab | 2330 | 2340 | HLA class I | HTMA | (Snyder et al., 2020) |
| ASRELKVTF | pp1ab | 1951 | 1959 | A*30:01/B*57:01 | AIM | (Tarke et al., 2021) |
| AYVDNSSLTI | pp1ab | 2098 | 2107 | A*24:02 | AIM | (Tarke et al., 2021) |
| AYVNTFSSTF | pp1ab | 2593 | 2602 | A*24:02 | AIM | (Tarke et al., 2021) |
| CATVHTANKW | pp1ab | 6913 | 6922 | B*57:01 | AIM | (Tarke et al., 2021) |
| CLEASFNYL | pp1ab | 2210 | 2218 | A*02:01 | ELISPOT | (Prakash et al., 2021) |
| CSLSHRFYR | pp1ab | 5038 | 5046 | A*11:01 | proliferation | (Jin et al., 2021) |
| CSQHTMLVK | pp1ab | 5205 | 5213 | A*11:01 | proliferation | (Jin et al., 2021) |
| CTDDNALAY | pp1ab | 4163 | 4171 | A*01:01 | ICS | (Schulien et al., 2021) |
| CTDDNALAYY | pp1ab | 4163 | 4172 | A*01:01 | ICS/multimer staining /AIM/ELISA/cytotoxicity | (Saini et al., 2021; Titov et al., 2022; Schulien et al., 2021; Ferretti et al., 2020; Gangaev et al., 2021) |
| CTEIDPKLDNY | pp1ab | 1889 | 1899 | A*01:01 | multimer staining | (Saini et al., 2021) |
| DAMRNAGIV | pp1ab | 4586 | 4594 | B*51:01 | AIM | (Tarke et al., 2021) |
| DASGKPVPY | pp1ab | 2924 | 2932 | B*35:01 | AIM | (Tarke et al., 2021) |
| DAVNLLTNM | pp1ab | 3022 | 3030 | B*51:01 | AIM | (Tarke et al., 2021) |
| DDYQGKPLEF | pp1ab | 953 | 962 | A*24:02 | multimer staining | (Saini et al., 2021) |
| DFYDFAVSKGFFK | pp1ab | 4810 | 4822 | A*33:01 | AIM | (Tarke et al., 2021) |
| DGTLMIERFVSLAID | pp1ab | 5243 | 5257 | HLA class I | ELISPOT | (Swadling et al., 2022) |
| DLKGKYVQI | pp1ab | 4344 | 4352 | B*08:01 | ICS/ELISPOT | (Nelde et al., 2021) |
| DSAEVAVKM | pp1ab | 2582 | 2590 | A*26:01 | AIM | (Tarke et al., 2021) |
| DSCNNYMLTY | pp1ab | 2668 | 2677 | A*01:01 | multimer staining | (Saini et al., 2021) |
| DTDFVNEFY | pp1ab | 5130 | 5138 | A*01:01 | ICS/ multimer staining /ELISA/cytotoxicity | (Wagner et al., 2022; Titov et al., 2022; Schulien et al., 2021; Swaminathan et al., 2022; Ferretti et al., 2020; Kared et al., 2021; Gangaev et al., 2021; Minervina et al., 2022) |
| DTFCAGSTF | pp1ab | 2456 | 2464 | A*26:01 | AIM | (Tarke et al., 2021) |
| DTIANYAKPF | pp1ab | 2136 | 2145 | A*26:01 | AIM | (Tarke et al., 2021) |
| DTVIEVQGYK | pp1ab | 828 | 837 | A*68:01 | AIM | (Tarke et al., 2021) |
| DVDTDFVNEFYAYLR | pp1ab | 5128 | 5142 | HLA class I | ELISPOT | (Swadling et al., 2022) |
| DVFYKENSY | pp1ab | 1865 | 1873 | A*26:01 | AIM | (Tarke et al., 2021) |
| DVLLPLTQY | pp1ab | 3196 | 3204 | B*35:01 | AIM | (Tarke et al., 2021) |
| DVVAIDYKHY | pp1ab | 1966 | 1975 | A*26:01 | AIM | (Tarke et al., 2021) |
| DYKHYTPSF | pp1ab | 1971 | 1979 | A*24:02 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| DYVYLPYPDPSRI | pp1ab | 5217 | 5229 | B*51:01 | AIM | (Tarke et al., 2021) |
| EAFEKMVSL | pp1ab | 3906 | 3914 | B*08:01 | ELISPOT | (Nelde et al., 2021) |
| EAKKVKPTV | pp1ab | 1048 | 1056 | B*51:01 | AIM | (Tarke et al., 2021) |
| EEAIRHVRAW | pp1ab | 6002 | 6011 | B*44:03 | ICS | (Schulien et al., 2021) |
| EEFEPSTQYEY | pp1ab | 939 | 949 | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| EEIAIILASF | pp1ab | 471 | 480 | B*44:03 | ICS | (Schulien et al., 2021) |
| EESSAKSASVY | pp1ab | 2550 | 2560 | B*44:02 | AIM | (Tarke et al., 2021) |
| EEVGHTDLMAAY | pp1ab | 2088 | 2099 | B*44:03 | AIM | (Tarke et al., 2021) |
| EEVVENPTI | pp1ab | 2049 | 2057 | B*44:03 | AIM | (Tarke et al., 2021) |
| EGYLNSTNV | pp1ab | 2268 | 2276 | B*51:01 | AIM | (Tarke et al., 2021) |
| EIDPKLDNY | pp1ab | 1891 | 1899 | A*26:01/A*01:01 | AIM | (Tarke et al., 2021) |
| EIKESVQTF | pp1ab | 670 | 678 | A*02:01/B*07:02/B*15:01 | multimer staining | (Saini et al., 2021; Weingarten-Gabbay et al., 2021) |
| ELDERIDKV | pp1ab | 844 | 852 | A*02:01 | multimer staining | (Saini et al., 2021) |
| ELKHFFFAQDGNAAI | pp1ab | 4828 | 4842 | A*24:02 | ELISPOT | (Swadling et al., 2022) |
| ERHSLSHFV | pp1ab | 2514 | 2522 | C*06:02 | multimer staining | (Saini et al., 2021) |
| ESKPSVEQR | pp1ab | 1217 | 1225 | A*68:01 | AIM | (Tarke et al., 2021) |
| ETIQITISSF | pp1ab | 2305 | 2314 | A*26:01 | AIM | (Tarke et al., 2021) |
| EVARDLSLQF | pp1ab | 2468 | 2477 | A*26:01 | AIM | (Tarke et al., 2021) |
| EVAVKMFDAY | pp1ab | 2585 | 2594 | A*26:01 | AIM | (Tarke et al., 2021) |
| EVGHTDLMAAY | pp1ab | 2089 | 2099 | A*26:01 | AIM | (Tarke et al., 2021) |
| EVKPFITESK | pp1ab | 1210 | 1219 | A*68:01 | AIM | (Tarke et al., 2021) |
| EVTGDSCNNYMLTY | pp1ab | 2664 | 2677 | A*26:01 | AIM | (Tarke et al., 2021) |
| FADDLNQLTGY | pp1ab | 1937 | 1947 | A*01:01 | AIM/HTMA | (Snyder et al., 2020; Tarke et al., 2021) |
| FAIGLALYY | pp1ab | 5615 | 5623 | C*07:02 | multimer staining | (Saini et al., 2021) |
| FASEAARVV | pp1ab | 536 | 544 | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| FAVDAAKAY | pp1ab | 4272 | 4280 | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| FAVSKGFFK | pp1ab | 4814 | 4822 | A*11:01 | AIM | (Tarke et al., 2021) |
| FAYTKRNVI | pp1ab | 4920 | 4928 | B*51:01 | AIM | (Tarke et al., 2021) |
| FDIYNDKVAGF | pp1ab | 4427 | 4437 | A*24:02 | multimer staining | (Saini et al., 2021) |
| FELDERIDKV | pp1ab | 843 | 852 | A*02:01 | AIM | (Tarke et al., 2021) |
| FELDERIDKVL | pp1ab | 843 | 853 | B*40:01 | AIM | (Tarke et al., 2021) |
| FEPSTQYEY | pp1ab | 941 | 949 | B*44:02 | AIM | (Tarke et al., 2021) |
| FEYYHTTDPSF | pp1ab | 1632 | 1642 | A*24:02 | multimer staining | (Saini et al., 2021) |
| FGDDTVIEV | pp1ab | 825 | 833 | A*02:01/B*07:02 | multimer staining | (Saini et al., 2021; Weingarten-Gabbay et al., 2021; Poran et al., 2020) |
| FGEYSHVVAF | pp1ab | 3071 | 3080 | B*40:01 | AIM | (Tarke et al., 2021) |
| FIERYKLEGY | pp1ab | 6673 | 6682 | A*01:01 | multimer staining | (Saini et al., 2021) |
| FIPMDSTVKNY | pp1ab | 6720 | 6730 | A*01:01 | multimer staining | (Saini et al., 2021) |
| FLAHIQWMV | pp1ab | 3122 | 3130 | A*02:06/A*02:01 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| FLARGIVFM | pp1ab | 3753 | 3761 | A*02:01 | multimer staining | (Saini et al., 2021) |
| FLCLFLLPSLATV | pp1ab | 3635 | 3647 | HLA class I | HTMA | (Snyder et al., 2020) |
| FLGRYMSAL | pp1ab | 1642 | 1650 | HLA class I | HTMA | (Snyder et al., 2020) |
| FLIGCNYL | pp1ab | 7003 | 7010 | A*02:01 | ICS/AIM/multimer staining | (Quiros-Fernandez et al., 2021) |
| FLLNKEMYL | pp1ab | 3183 | 3191 | A*02:01/C*12:03 | ELISPOT/ELISA/HTMA/multimer staining/ICS | (Snyder et al., 2020; Habel et al., 2020; Titov et al., 2022; Prakash et al., 2021) |
| FLLPSLATV | pp1ab | 3639 | 3647 | A*02:01/C*07:01 | ICS/multimer staining | (Schulien et al., 2021; Poran et al., 2020; Nagler et al., 2021) |
| FLLPSLATVA | pp1ab | 3639 | 3648 | A*02:01 | multimer staining | (Saini et al., 2021) |
| FLNGSCGSV | pp1ab | 3403 | 3411 | HLA class I | HTMA | (Snyder et al., 2020) |
| FLNRFTTTL | pp1ab | 3482 | 3490 | HLA class I | HTMA | (Snyder et al., 2020) |
| FLPGVYSV | pp1ab | 3100 | 3107 | A*02:01 | AIM | (Tarke et al., 2021) |
| FLPRVFSAV | pp1ab | 2884 | 2892 | A*02:01 | AIM/HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020; Tarke et al., 2021) |
| FLTENLLLYI | pp1ab | 1248 | 1257 | A*02:01 | multimer staining | (Saini et al., 2021) |
| FLYENAFLP | pp1ab | 3605 | 3613 | A*02:01 | AIM | (Tarke et al., 2021) |
| FLYENAFLPFA | pp1ab | 3605 | 3615 | A*02:01 | multimer staining | (Saini et al., 2021) |
| FNKWGKARLYYDSMS | pp1ab | 4898 | 4912 | HLA class I | ELISPOT | (Swadling et al., 2022) |
| FPLKLRGTA | pp1ab | 7048 | 7056 | B*07:02 | AIM | (Tarke et al., 2021) |
| FPLKLRGTAV | pp1ab | 7048 | 7057 | B*08:01 | multimer staining | (Saini et al., 2021) |
| FPPTSFGPL | pp1ab | 4713 | 4721 | HLA class I | HTMA | (Snyder et al., 2020) |
| FRYMNSQGL | pp1ab | 3820 | 3828 | HLA class I | ELISA/HTMA | (Snyder et al., 2020; Titov et al., 2022) |
| FSAVGNICY | pp1ab | 2889 | 2897 | A*01:01 | multimer staining | (Saini et al., 2021) |
| FTCASEYTGNY | pp1ab | 1821 | 1831 | A*01:01 | multimer staining | (Saini et al., 2021) |
| FTDGVCLFW | pp1ab | 6302 | 6310 | A*01:01 | multimer staining | (Saini et al., 2021) |
| FTEQPIDLVPNQPY | pp1ab | 1907 | 1920 | HLA class I | HTMA | (Snyder et al., 2020) |
| FTSLEIPRRNVATLQ | pp1ab | 5911 | 5925 | HLA class I | ELISPOT | (Swadling et al., 2022) |
| FTYASALWEI | pp1ab | 4089 | 4098 | HLA class I | HTMA | (Snyder et al., 2020) |
| FVDGVPFVV | pp1ab | 4726 | 4734 | A*02:07/A*02:01 | ICS/HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020; Swaminathan et al., 2022) |
| FVENPDILRV | pp1ab | 4557 | 4566 | A*02:06 | AIM | (Tarke et al., 2021) |
| FVKHKHAFL | pp1ab | 3628 | 3636 | B*08:01 | ICS/ELISPOT | (Wagner et al., 2022; Nelde et al., 2021) |
| FVNEFYAYL | pp1ab | 5133 | 5141 | A*02:01 | multimer staining/ICS | (Saini et al., 2021; Jin et al., 2021) |
| FVNEFYAYLR | pp1ab | 5133 | 5142 | A*33:01 | AIM | (Tarke et al., 2021) |
| FVVEVVDKY | pp1ab | 4863 | 4871 | B*15:01 | multimer staining | (Saini et al., 2021) |
| FVVPGLPGT | pp1ab | 2864 | 2872 | A*02:06 | AIM | (Tarke et al., 2021) |
| FVVSTGYHFR | pp1ab | 4732 | 4741 | A*68:01 | AIM | (Tarke et al., 2021) |
| FWRNTNPIQL | pp1ab | 7028 | 7037 | C*07:01 | multimer staining | (Saini et al., 2021) |
| FYAYLRKHF | pp1ab | 5137 | 5145 | A*24:02 | ICS/multimer staining | (Saini et al., 2021) |
| FYLITPVHV | pp1ab | 2787 | 2795 | C*07:02 | multimer staining | (Saini et al., 2021) |
| FYYVWKSY | pp1ab | 2390 | 2397 | C*07:02 | multimer staining | (Saini et al., 2021) |
| FYYVWKSYV | pp1ab | 2390 | 2398 | C*06:02/C*07:02 | multimer staining | (Saini et al., 2021) |
| GADPIHSLR | pp1ab | 1155 | 1163 | A*68:01 | AIM | (Tarke et al., 2021) |
| GAMDTTSYR | pp1ab | 3219 | 3227 | A*31:01 | AIM | (Tarke et al., 2021) |
| GEAANFCAL | pp1ab | 1705 | 1713 | B*40:01 | ICS | (Schulien et al., 2021) |
| GELGDVRETMSYLF | pp1ab | 1723 | 1736 | B*44:02 | AIM | (Tarke et al., 2021) |
| GETLPTEVL | pp1ab | 744 | 752 | B*40:01 | ICS | (Schulien et al., 2021) |
| GEVITFDNL | pp1ab | 1548 | 1556 | B*40:01 | ICS | (Schulien et al., 2021) |
| GFMGRIRSV | pp1ab | 295 | 303 | C*06:02 | multimer staining | (Saini et al., 2021) |
| GLLPPKNSI | pp1ab | 3827 | 3835 | A*02:01 | multimer staining | (Saini et al., 2021) |
| GNAAISDYDYYRYNl | pp1ab | 4838 | 4852 | B*35:01 | ELISPOT | (Swadling et al., 2022) |
| GPKVKYLYF | pp1ab | 4222 | 4230 | B*08:01 | multimer staining | (Saini et al., 2021) |
| GPPGTGKSHFAIGLA | pp1ab | 282 | 296 | HLA class I | ICS/AIM | (Eggenhuizen et al., 2021) |
| GRVDGQVDL | pp1ab | 6577 | 6585 | C*07:01 | multimer staining | (Saini et al., 2021) |
| GSVAYESLR | pp1ab | 2941 | 2949 | A*31:01 | AIM | (Tarke et al., 2021) |
| GTDLEGNFY | pp1ab | 3437 | 3445 | A*01:01 | ELISA/ICS/cytotoxicity/multimer staining | (Wagner et al., 2022; Titov et al., 2022; Ferretti et al., 2020; Kared et al., 2021) |
| GTSTDVVYR | pp1ab | 4417 | 4425 | A*11:01 | proliferation | (Jin et al., 2021) |
| GVAMPNLYK | pp1ab | 6806 | 6814 | HLA class I | HTMA | (Snyder et al., 2020) |
| GVAPGTAVLRQW | pp1ab | 6875 | 6886 | B*57:01 | AIM | (Tarke et al., 2021) |
| GVYDYLVST | pp1ab | 3809 | 3817 | A*02:01 | multimer staining | (Saini et al., 2021) |
| HFISNSWLMW | pp1ab | 2357 | 2366 | A*24:02 | multimer staining | (Saini et al., 2021) |
| HLDGEVITF | pp1ab | 1545 | 1553 | C*07:02 | multimer staining | (Saini et al., 2021) |
| HLKDGTCGL | pp1ab | 45 | 53 | B*08:01 | multimer staining | (Saini et al., 2021) |
| HNDILLAKDTTEAFE | pp1ab | 3895 | 3909 | B*35:03 | ICS | (Le Bert et al., 2020) |
| HSIGFDYVY | pp1ab | 6154 | 6162 | B*35:01 | ICS | (Wagner et al., 2022) |
| HTDFSSEIIGY | pp1ab | 2799 | 2809 | HLA class I | HTMA | (Snyder et al., 2020) |
| HTQVVDMSMTY | pp1ab | 1580 | 1590 | A*01:01 | multimer staining | (Saini et al., 2021) |
| HTTDPSFLGR | pp1ab | 1636 | 1645 | A*68:01 | AIM | (Tarke et al., 2021) |
| HTTDPSFLGRY | pp1ab | 1636 | 1646 | A*01:01 | AIM/ELISA/HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020; Tarke et al., 2021; Titov et al., 2022; Kared et al., 2021) |
| HVDTDLTKPY | pp1ab | 4648 | 4657 | A*01:01 | multimer staining | (Saini et al., 2021) |
| HVGEIPVAY | pp1ab | 110 | 118 | B*15:01 | multimer staining | (Saini et al., 2021) |
| IAATRGATV | pp1ab | 4971 | 4979 | B*51:01 | AIM | (Tarke et al., 2021) |
| IAAVITREV | pp1ab | 2854 | 2862 | B*51:01 | AIM | (Tarke et al., 2021) |
| IEVNSFSGY | pp1ab | 1023 | 1031 | B*44:02 | AIM | (Tarke et al., 2021) |
| IEYPIIGDEL | pp1ab | 6219 | 6228 | B*40:01 | ELISPOT | (Nelde et al., 2021) |
| IFFITGNTL | pp1ab | 3768 | 3776 | A*24:02 | multimer staining | (Saini et al., 2021) |
| IIWFLLLSV | pp1ab | 2230 | 2238 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| ILFTRFFYV | pp1ab | 2332 | 2340 | A*02:01 | ICS/AIM | (Tarke et al., 2021; Habel et al., 2020; Schulien et al., 2021) |
| ILGLPTQTV | pp1ab | 5849 | 5857 | A*02:01 | HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020) |
| ILHCANFNV | pp1ab | 4699 | 4707 | A*02:01 | HTMA/ICS | (Snyder et al., 2020; Jin et al., 2021) |
| ILMTARTVY | pp1ab | 3693 | 3701 | B*15:01 | multimer staining | (Gangaev et al., 2021) |
| ILSPLYAFA | pp1ab | 529 | 537 | A*02:01 | multimer staining | (Saini et al., 2021) |
| ILTSLLVLV | pp1ab | 3587 | 3595 | A*02:01 | multimer staining | (Saini et al., 2021) |
| IMASLVLAR | pp1ab | 5024 | 5032 | A*33:01 | AIM | (Tarke et al., 2021) |
| IPARARVEC | pp1ab | 5658 | 5666 | B*07:02 | multimer staining | (Saini et al., 2021) |
| IPARARVECF | pp1ab | 5658 | 5667 | B*07:02 | multimer staining | (Saini et al., 2021) |
| IPRRNVATL | pp1ab | 5916 | 5924 | B*08:01/B*07:02 | ICS/multimer staining/HTMA/ELISA/cytotoxicity | (Saini et al., 2021; Snyder et al., 2020; Schulien et al., 2021; Ferretti et al., 2020; Kared et al., 2021; Gangaev et al., 2021) |
| IPTITQMNL | pp1ab | 4928 | 4936 | B*07:02 | multimer staining | (Saini et al., 2021) |
| IPVAYRKVLL | pp1ab | 114 | 123 | B*07:02 | multimer staining | (Saini et al., 2021) |
| IQITISSFK | pp1ab | 2307 | 2315 | A*03:01 | multimer staining | (Saini et al., 2021) |
| IQPGQTFSV | pp1ab | 3369 | 3377 | HLA class I | HTMA | (Snyder et al., 2020) |
| ISLAGSYKDW | pp1ab | 1505 | 1514 | B*57:01 | AIM | (Tarke et al., 2021) |
| ISTKHFYW | pp1ab | 3148 | 3155 | B*57:01 | AIM | (Tarke et al., 2021) |
| ITDVFYKENSY | pp1ab | 1863 | 1873 | A*01:01 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| ITEEVGHTDLMAAY | pp1ab | 2086 | 2099 | A*01:01 | AIM/HTMA | (Snyder et al., 2020; Tarke et al., 2021) |
| ITFDNLKTL | pp1ab | 1551 | 1559 | B*57:01 | AIM | (Tarke et al., 2021) |
| IVAGGIVAI | pp1ab | 3047 | 3055 | A*02:01 | multimer staining | (Saini et al., 2021) |
| IVDTVSALV | pp1ab | 5772 | 5780 | HLA class I | HTMA | (Snyder et al., 2020) |
| IVDTVSALVY | pp1ab | 5772 | 5781 | A*01:01 | multimer staining/ cytotoxicity/ICS/AIM | (Pan et al., 2021) |
| ISDYDYYRY | pp1ab | 4842 | 4850 | HLA class I | HTMA | (Snyder et al., 2020) |
| ITILDGISQY | pp1ab | 567 | 576 | B*15:01 | multimer staining | (Saini et al., 2021) |
| IYLYLTFYL | pp1ab | 3108 | 3116 | A*24:02 | AIM | (Tarke et al., 2021) |
| KASMPTTIA | pp1ab | 2191 | 2199 | A*30:01 | AIM | (Tarke et al., 2021) |
| KENSYTTTIKPVTY | pp1ab | 1869 | 1882 | B*44:02 | AIM | (Tarke et al., 2021) |
| KFADDLNQL | pp1ab | 1936 | 1944 | C*07:02 | multimer staining | (Saini et al., 2021) |
| KFCLEASFNY | pp1ab | 2208 | 2217 | A*29:02 | AIM | (Tarke et al., 2021) |
| KIAEIPKEEV | pp1ab | 1202 | 1211 | A*02:01 | multimer staining | (Saini et al., 2021) |
| KIEELFYSY | pp1ab | 6287 | 6295 | B*15:01 | multimer staining | (Saini et al., 2021) |
| KIFVDGVPFV | pp1ab | 4724 | 4733 | A*02:01 | multimer staining/ICS | (Saini et al., 2021; Jin et al., 2021) |
| KLFAAETLK | pp1ab | 5455 | 5463 | A*03:01 | HTMA/multimer staining/cytotoxicity/AIM/ICS/ELISPOT | (Snyder et al., 2020; Nelde et al., 2021; Pan et al., 2021) |
| KLFDRYFKY | pp1ab | 4673 | 4681 | A*03:01/A*11:01 | multimer staining/ICS | (Saini et al., 2021; Wagner et al., 2022; Kared et al., 2021) |
| KLINIIIWF | pp1ab | 2225 | 2233 | A*32:01 | AIM | (Tarke et al., 2021) |
| KLINITIWFL | pp1ab | 2225 | 2234 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| KLKDCVMYA | pp1ab | 3678 | 3686 | A*02:01 | multimer staining | (Saini et al., 2021) |
| KLLHKPIVWHV | pp1ab | 1984 | 1994 | A*02:01 | multimer staining | (Saini et al., 2021) |
| KLMGHFAWW | pp1ab | 6980 | 6988 | A*32:01 | AIM | (Tarke et al., 2021) |
| KLMPVCVET | pp1ab | 1387 | 1395 | A*02:01 | multimer staining | (Saini et al., 2021) |
| KLNIKLLGV | pp1ab | 3839 | 3847 | A*02:01 | multimer staining | (Saini et al., 2021) |
| KLNVGDYFV | pp1ab | 5542 | 5550 | A*02:01 | HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020) |
| KLSYGIATV | pp1ab | 5470 | 5478 | A*02:01 | ELISPOT/HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020; Prakash et al., 2021) |
| KLVNKFLAL | pp1ab | 680 | 688 | A*02:01 | multimer staining | (Saini et al., 2021) |
| KLVSSFLEM | pp1ab | 1185 | 1193 | B*15:01 | multimer staining | (Saini et al., 2021) |
| KLWAQCVQL | pp1ab | 3886 | 3894 | A*02:01/B*07:02 | ELISA/HTMA/multimer staining/ELISPOT/ICS/cytotoxicity | (Saini et al., 2021; Snyder et al., 2020; Weingarten-Gabbay et al., 2021; Wagner et al., 2022; Titov et al., 2022; Ferretti et al., 2020; Swadling et al., 2022) |
| KMADQAMTQMY | pp1ab | 4003 | 4013 | B*15:01 | multimer staining | (Saini et al., 2021) |
| KMFDAYVNTF | pp1ab | 2589 | 2598 | A*24:02 | AIM | (Tarke et al., 2021) |
| KMQRMLLEK | pp1ab | 6814 | 6822 | HLA class I | HTMA | (Snyder et al., 2020) |
| KMVSLLSVLLSMQGA | pp1ab | 3910 | 3924 | HLA class I | ELISPOT | (Swadling et al., 2022) |
| KNLSDRVVFV | pp1ab | 6100 | 6109 | A*02:01 | multimer staining | (Saini et al., 2021) |
| KPHNSHEGKTF | pp1ab | 1608 | 1618 | B*07:02 | multimer staining | (Saini et al., 2021) |
| KPLEFGATSAAL | pp1ab | 958 | 969 | HLA class I | HTMA | (Snyder et al., 2020) |
| KPNELSRVL | pp1ab | 2109 | 2117 | B*07:02/B*08:01 | AIM/ICS/multimer staining | (Saini et al., 2021; Tarke et al., 2021; Wagner et al., 2022) |
| KPPISFPL | pp1ab | 5400 | 5407 | B*07:02 | multimer staining | (Saini et al., 2021) |
| KPRSQMEIDF | pp1ab | 6656 | 6665 | B*07:02 | multimer staining | (Saini et al., 2021) |
| KPVETSNSFDVL | pp1ab | 2017 | 2028 | B*07:02 | AIM | (Tarke et al., 2021) |
| KPYIKWDLL | pp1ab | 4655 | 4663 | B*07:02 | multimer staining | (Saini et al., 2021) |
| KQEILGTVSW | pp1ab | 1364 | 1373 | B*44:02/B*44:03 | AIM | (Tarke et al., 2021) |
| KQFDTYNLW | pp1ab | 6437 | 6445 | B*15:01 | ELISA/HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020; Titov et al., 2022) |
| KQGDDYVYL | pp1ab | 5213 | 5221 | A*02:01 | multimer staining | (Saini et al., 2021) |
| KQLIKVTLVF | pp1ab | 2771 | 2780 | B*15:01 | ICS | (Schulien et al., 2021) |
| KRVDWTIEY | pp1ab | 6213 | 6221 | B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| KSAGFPFNK | pp1ab | 4892 | 4900 | A*03:01/A*11:01 | AIM/proliferation | (Tarke et al., 2021; Jin et al., 2021) |
| KSAGFPFNKW | pp1ab | 4892 | 4901 | B*57:01 | AIM | (Tarke et al., 2021) |
| KTIQPRVEK | pp1ab | 282 | 290 | A*30:01/A*11:01/A*03:01 | ELISA/ICS/cytotoxicity/multimer staining | (Wagner et al., 2022; Titov et al., 2022; Ferretti et al., 2020; Kared et al., 2021) |
| KTNCCRFQEK | pp1ab | 4442 | 4451 | A*11:01 | proliferation | (Jin et al., 2021) |
| KVAGFAKFL | pp1ab | 4433 | 4441 | A*32:01 | AIM | (Tarke et al., 2021) |
| KVAGFAKFLK | pp1ab | 4433 | 4442 | A*11:01 | AIM | (Tarke et al., 2021) |
| KVDGVDVEL | pp1ab | 6486 | 6494 | A*02:01 | multimer staining | (Saini et al., 2021) |
| KVDGVVQQL | pp1ab | 6633 | 6641 | A*02:01 | multimer staining | (Saini et al., 2021) |
| LATNNLVVM | pp1ab | 590 | 598 | B*07:02/A*02:01 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| LAYYFMRFR | pp1ab | 3060 | 3068 | A*31:01 | AIM | (Tarke et al., 2021) |
| LEFGATSAAL | pp1ab | 960 | 969 | B*40:01 | AIM | (Tarke et al., 2021) |
| LEIPRRNVATL | pp1ab | 5914 | 5924 | B*07:02 | multimer staining | (Saini et al., 2021) |
| LEMELTPVV | pp1ab | 1012 | 1020 | B*40:01 | AIM | (Tarke et al., 2021) |
| LFLLPSLATV | pp1ab | 3638 | 3647 | A*02:01 | multimer staining | (Saini et al., 2021) |
| LGDVRETMSY | pp1ab | 1725 | 1734 | A*01:01 | multimer staining | (Saini et al., 2021) |
| LHKPIVWHV | pp1ab | 1986 | 1994 | C*06:02 | multimer staining | (Saini et al., 2021) |
| LKKLKKSL | pp1ab | 3977 | 3984 | B*08:01 | multimer staining | (Saini et al., 2021) |
| LLADKFPVL | pp1ab | 6246 | 6254 | A*02:01/B*08:01 | ICS/AIM/multimer staining | (Saini et al., 2021; Quiros-Fernandez et al., 2021) |
| LLLDDFVEI | pp1ab | 6749 | 6757 | A*02:01 | ELISPOT | (Prakash et al., 2021) |
| LLLDDFVEII | pp1ab | 6749 | 6758 | HLA class I | HTMA | (Snyder et al., 2020) |
| LLSAGIFGA | pp1ab | 1148 | 1156 | HLA class I | HTMA | (Snyder et al., 2020) |
| LMIERFVSL | pp1ab | 5246 | 5254 | A*02:01 | HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020) |
| LMVVIPDYNTY | pp1ab | 4070 | 4080 | B*15:01 | multimer staining | (Saini et al., 2021) |
| LPFAMGIIAM | pp1ab | 3612 | 3621 | B*07:02 | AIM | (Tarke et al., 2021) |
| LPGVYSVI | pp1ab | 3101 | 3108 | B*51:01 | AIM | (Tarke et al., 2021) |
| LPKGIMMNV | pp1ab | 6834 | 6842 | B*07:02 | multimer staining | (Saini et al., 2021) |
| LPLTQYNRY | pp1ab | 3199 | 3207 | B*35:01 | AIM | (Tarke et al., 2021) |
| LPRVFSAV | pp1ab | 2885 | 2892 | B*51:01 | AIM | (Tarke et al., 2021) |
| LPYPDPSRI | pp1ab | 5221 | 5229 | B*51:01 | multimer staining/ICS | (Swaminathan et al., 2022; Gangaev et al., 2021) |
| LPYPDPSRIL | pp1ab | 5221 | 5230 | B*51:01/B*07:02 | AIM/ELISPOT/AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021; Ma et al., 2021) |
| LQGPPGTGKSHFAIG | pp1ab | 5612 | 5626 | HLA class I | ICS/AIM/AIM | (Eggenhuizen et al., 2021) |
| LQLGFSTGV | pp1ab | 6032 | 6040 | HLA class I | HTMA | (Snyder et al., 2020) |
| LRAKHYVYIGDPAQL | pp1ab | 5715 | 5729 | HLA class I | ELISPOT | (Swadling et al., 2022) |
| LRGTAVMSL | pp1ab | 7052 | 7060 | C*07:01 | multimer staining | (Saini et al., 2021) |
| LRIMASLVL | pp1ab | 5022 | 5030 | C*07:02 | multimer staining | (Saini et al., 2021) |
| LRKHFSMMI | pp1ab | 5141 | 5149 | C*06:02 | multimer staining | (Saini et al., 2021) |
| LRPDTRYV | pp1ab | 2948 | 2955 | C*06:02 | multimer staining | (Saini et al., 2021) |
| LRVEAFEYY | pp1ab | 1627 | 1635 | C*07:01 | multimer staining | (Saini et al., 2021) |
| LSDDAVVCFNSTY | pp1ab | 5150 | 5162 | HLA class I | HTMA | (Snyder et al., 2020) |
| LSFKELLVYA | pp1ab | 4758 | 4767 | A*02:06 | ICS | (Jin et al., 2021) |
| LLMPILTLT | pp1ab | 4632 | 4640 | HLA class I | HTMA | (Snyder et al., 2020) |
| LTAFGLVAEW | pp1ab | 2318 | 2327 | B*57:01 | AIM | (Tarke et al., 2021) |
| LTAVVIPTK | pp1ab | 1296 | 1304 | A*68:01 | AIM | (Tarke et al., 2021) |
| LTGHMLDMY | pp1ab | 5287 | 5295 | A*01:01 | multimer staining | (Gangaev et al., 2021) |
| LTIKKPNEL | pp1ab | 2105 | 2113 | B*08:01 | multimer staining | (Saini et al., 2021) |
| LTNDNTSRYW | pp1ab | 5299 | 5308 | B*57:01 | AIM | (Tarke et al., 2021) |
| LTNIFGTVY | pp1ab | 613 | 621 | A*01:01 | ICS | (Wagner et al., 2022) |
| LVAEWFLAY | pp1ab | 2323 | 2331 | A*26:01/A*29:02/B*35:01 | AIM/ICS | (Tarke et al., 2021; Wagner et al., 2022) |
| LVKQGDDYVY | pp1ab | 5211 | 5220 | B*15:01 | multimer staining | (Saini et al., 2021) |
| LVLSVNPYV | pp1ab | 5365 | 5373 | HLA class I | HTMA | (Snyder et al., 2020) |
| LVQMAPISAM | pp1ab | 2371 | 2380 | B*15:01 | ICS | (Schulien et al., 2021) |
| LVSDIDITF | pp1ab | 1270 | 1278 | B*35:01 | AIM | (Tarke et al., 2021) |
| LYDKLVSSF | pp1ab | 1182 | 1190 | A*24:02 | AIM | (Tarke et al., 2021) |
| LYLQYIRKL | pp1ab | 5275 | 5283 | C*07:02 | multimer staining | (Saini et al., 2021) |
| LYQPPQTSI | pp1ab | 3249 | 3257 | A*24:02/C*07:01 | multimer staining | (Saini et al., 2021) |
| LYYQNNVFM | pp1ab | 5178 | 5186 | A*24:02 | multimer staining | (Saini et al., 2021) |
| MASLVLARK | pp1ab | 5025 | 5033 | A*68:01 | AIM | (Tarke et al., 2021) |
| MELTPVVQTI | pp1ab | 1014 | 1023 | B*40:01 | AIM | (Tarke et al., 2021) |
| MFDAYVNTF | pp1ab | 2590 | 2598 | B*08:01 | multimer staining | (Saini et al., 2021) |
| MFTPLVPFW | pp1ab | 3131 | 3139 | A*24:02 | AIM | (Tarke et al., 2021) |
| MFVKHKHAF | pp1ab | 3627 | 3635 | C*07:02 | multimer staining | (Saini et al., 2021) |
| MLAHAEETR | pp1ab | 1378 | 1386 | A*68:01 | AIM | (Tarke et al., 2021) |
| MLDMYSVML | pp1ab | 5291 | 5299 | A*02:01/A*02:03 | ICS/proliferation | (Jin et al., 2021) |
| MLLGSMLYM | pp1ab | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) | ||
| MLRIMASL | pp1ab | 5021 | 5028 | B*08:01 | multimer staining | (Saini et al., 2021) |
| MLWCKDGHV | pp1ab | 6782 | 6790 | HLA class I | HTMA | (Snyder et al., 2020) |
| MMISAGFSL | pp1ab | 6425 | 6433 | A*02:01 | HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020) |
| MPASWVMRI | pp1ab | 3655 | 3663 | B*07:02 | AIM/HTMA/ELISA/multimer staining | (Saini et al., 2021; Snyder et al., 2020; Tarke et al., 2021; Titov et al., 2022) |
| MPNMLRIMASL | pp1ab | 5018 | 5028 | B*07:02 | multimer staining | (Saini et al., 2021) |
| MPTTIAKNTV | pp1ab | 2194 | 2203 | B*51:01 | AIM | (Tarke et al., 2021) |
| MPYFFTLL | pp1ab | 2169 | 2176 | B*51:01 | AIM | (Tarke et al., 2021) |
| MSALNHTKK | pp1ab | 1647 | 1655 | A*30:01 | AIM | (Tarke et al., 2021) |
| MSALNHTKKW | pp1ab | 1647 | 1656 | B*57:01 | AIM | (Tarke et al., 2021) |
| MSMTYGQQF | pp1ab | 1586 | 1594 | B*57:01 | AIM | (Tarke et al., 2021) |
| MSNLGMPSY | pp1ab | 2254 | 2262 | B*57:01/B*15:01 | AIM | (Tarke et al., 2021) |
| MTNRQFHQK | pp1ab | 4958 | 4966 | A*30:01 | proliferation | (Jin et al., 2021) |
| MVMCGGSLYV | pp1ab | 5058 | 5067 | HLA class I | HTMA | (Snyder et al., 2020) |
| MVTNNTFTLK | pp1ab | 807 | 816 | A*03:01 | ELISA | (Titov et al., 2022) |
| MYASAVVLL | pp1ab | 3684 | 3692 | C*07:02 | multimer staining | (Saini et al., 2021) |
| MYKGLPWNV | pp1ab | 6078 | 6086 | C*06:02 | multimer staining | (Saini et al., 2021) |
| NAAISDYDY | pp1ab | 4839 | 4847 | B35 | ELISPOT | (Swadling et al., 2022) |
| NELSRVLGL | pp1ab | 2111 | 2119 | B*44:02/B*40:01 | AIM | (Tarke et al., 2021) |
| NINLHTQVV | pp1ab | 1576 | 1584 | B*08:01 | multimer staining | (Saini et al., 2021) |
| NKATYKPNTW | pp1ab | 1999 | 2008 | B*57:01 | AIM | (Tarke et al., 2021) |
| NKLCEEMLDNRATLQ | pp1ab | 3928 | 3942 | HLA class I | ELISPOT | (Swadling et al., 2022) |
| NLHSSRLSF | pp1ab | 4752 | 4760 | B*08:01 | multimer staining | (Saini et al., 2021) |
| NLIDSYFVV | pp1ab | 4456 | 4464 | A*02:01 | multimer staining | (Kared et al., 2021) |
| NLKTLLSL | pp1ab | 1555 | 1562 | B*08:01 | multimer staining | (Saini et al., 2021) |
| NLLKDCPAV | pp1ab | 4480 | 4488 | A*02:07 | proliferation | (Jin et al., 2021) |
| NLWNTFTRL | pp1ab | 6443 | 6451 | A*02:01 | HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020) |
| NLYDKLVSSFL | pp1ab | 1181 | 1191 | A*02:01 | multimer staining | (Saini et al., 2021) |
| NMLRIMASL | pp1ab | 5020 | 5028 | A*02:01 | HTMA/ICS | (Snyder et al., 2020; Jin et al., 2021) |
| NPIQLSSYSL | pp1ab | 7033 | 7042 | B*07:02 | AIM | (Tarke et al., 2021) |
| NPKTPKYKF | pp1ab | 3358 | 3366 | B*07:02 | multimer staining | (Saini et al., 2021) |
| NRDVDTDFVNEFYAY | pp1ab | 5126 | 5140 | HLA class I | HTMA | (Snyder et al., 2020) |
| NRYFRLTL | pp1ab | 3801 | 3808 | C*06:02/C*07:02 | multimer staining | (Saini et al., 2021) |
| NSFSGYLKL | pp1ab | 1026 | 1034 | C*06:02 | multimer staining | (Saini et al., 2021) |
| NSTNVTIATY | pp1ab | 2272 | 2281 | A*26:01 | AIM | (Tarke et al., 2021) |
| NTCDGTTFTY | pp1ab | 4082 | 4091 | A*01:01 | ELISA/cytotoxicity | (Titov et al., 2022; Ferretti et al., 2020) |
| NTFTRLQSL | pp1ab | 6446 | 6454 | C*07:01 | multimer staining | (Saini et al., 2021) |
| NTSRYWEPEFY | pp1ab | 5303 | 5313 | A*01:01 | multimer staining | (Saini et al., 2021) |
| NTVKSVGKF | pp1ab | 2201 | 2209 | A*26:01 | AIM | (Tarke et al., 2021) |
| NVIPTITQM | pp1ab | 4926 | 4934 | C*07:01 | multimer staining | (Saini et al., 2021) |
| NVIPTITQMNL | pp1ab | 4926 | 4936 | A*02:05 | ICS | (Swaminathan et al., 2022) |
| NVKDFMSL | pp1ab | 2714 | 2721 | B*08:01 | multimer staining | (Saini et al., 2021) |
| NYMPYFFTL | pp1ab | 2167 | 2175 | A*24:02 | ICS/AIM/multimer staining | (Tarke et al., 2021; Schulien et al., 2021; Kared et al., 2021) |
| NYSGVVTTVMF | pp1ab | 3743 | 3753 | HLA class I | HTMA | (Snyder et al., 2020) |
| NYYKKDNSY | pp1ab | 1898 | 1906 | C*07:02 | multimer staining | (Saini et al., 2021) |
| PFMIDVQQW | pp1ab | 6164 | 6172 | A*24:02 | multimer staining | (Saini et al., 2021) |
| PTDNYITTY | pp1ab | 1321 | 1329 | A*01:01 | multimer staining /ELISA/cytotoxicity | (Saini et al., 2021; Titov et al., 2022; Ferretti et al., 2020; Kared et al., 2021; Gangaev et al., 2021; Minervina et al., 2022) |
| QEILGTVSW | pp1ab | 1365 | 1373 | B*44:03 | ICS/AIM | (Tarke et al., 2021; Schulien et al., 2021) |
| QEYADVFHLY | pp1ab | 5267 | 5276 | B*44:03/A*29:02 | ICS/AIM | (Tarke et al., 2021; Schulien et al., 2021) |
| QGYKSVNITF | pp1ab | 834 | 843 | A*24:02 | multimer staining | (Saini et al., 2021) |
| QIDGYVMHANYIFWR | pp1ab | 7016 | 7030 | HLA class I | ELISPOT | (Mateus et al., 2020) |
| QKYSTLQGPPGTGKS | pp1ab | 275 | 289 | HLA class I | ICS/AIM/AIM | (Eggenhuizen et al., 2021) |
| QLLFVVEVV | pp1ab | 4860 | 4868 | A*02:01 | ICS | (Jin et al., 2021) |
| QLMCQPILLL | pp1ab | 2563 | 2572 | HLA class I | HTMA | (Snyder et al., 2020) |
| QLYLGGMSYY | pp1ab | 5386 | 5395 | B*15:01 | multimer staining | (Saini et al., 2021) |
| QPGQTFSVL | pp1ab | 3370 | 3378 | B*07:02 | multimer staining | (Kared et al., 2021) |
| QPYVFIKRSDARTAP | pp1ab | 66 | 80 | HLA class I | ELISPOT | (Mateus et al., 2020) |
| QSDIEVTGDSCNNY | pp1ab | 2660 | 2673 | A*01:01 | AIM | (Tarke et al., 2021) |
| QTVKPGNFNK | pp1ab | 4800 | 4809 | A*11:01 | AIM | (Tarke et al., 2021) |
| QVVDMSMTY | pp1ab | 1582 | 1590 | A*11:01/A*01:01 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| QVVNVVTTK | pp1ab | 2749 | 2757 | A*03:01 | AIM | (Tarke et al., 2021) |
| REQIDGYVMHANY | pp1ab | 7014 | 7026 | B*44:02 | AIM | (Tarke et al., 2021) |
| RIKASMPTT | pp1ab | 2189 | 2197 | A*30:01 | AIM | (Tarke et al., 2021) |
| RILGAGCFV | pp1ab | 5228 | 5236 | HLA class I | HTMA | (Snyder et al., 2020) |
| RIMTWLDMV | pp1ab | 3662 | 3670 | A*02:01 | multimer staining | (Saini et al., 2021) |
| RLANECAQV | pp1ab | 5046 | 5054 | A*02:01 | multimer staining/ICS | (Saini et al., 2021; Jin et al., 2021) |
| RLIDAMMFT | pp1ab | 579 | 587 | A*02:01 | multimer staining | (Saini et al., 2021) |
| RLYYDSMSY | pp1ab | 4905 | 4913 | B*15:01 | HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020) |
| RMYIFFASFY | pp1ab | 2382 | 2391 | A*03:01 | ICS | (Schulien et al., 2021) |
| RPDTRYVL | pp1ab | 2949 | 2956 | B*07:02 | ELISA/cytotoxicity | (Ferretti et al., 2020) |
| RPDTRYVLM | pp1ab | 2949 | 2957 | B*35:01/B*07:02 | AIM/multimer staining | (Tarke et al., 2021; Kared et al., 2021) |
| RPQIGVVREF | pp1ab | 5814 | 5823 | B*15:01 | multimer staining | (Saini et al., 2021) |
| RQFHQKLLK | pp1ab | 4961 | 4969 | A*11:01 | ELISA | (Titov et al., 2022) |
| RQLLFVVEV | pp1ab | 4859 | 4867 | A*02:01 | HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020) |
| RTIKVFTTV | pp1ab | 1566 | 1574 | A*02:01 | multimer staining | (Saini et al., 2021) |
| RTNVYLAVF | pp1ab | 1170 | 1178 | B*57:01 | AIM | (Tarke et al., 2021) |
| RTTNGDFLHF | pp1ab | 2875 | 2884 | B*57:01 | AIM | (Tarke et al., 2021) |
| RVESSSKLWAQCVQL | pp1ab | 3880 | 3894 | A*02:01 | ELISPOT | (Swadling et al., 2022) |
| RYFKYWDQTY | pp1ab | 4677 | 4686 | A*24:02 | multimer staining | (Saini et al., 2021) |
| SAFAMMFVK | pp1ab | 3622 | 3630 | A*11:01 | ICS/multimer staining | (Schulien et al., 2021; Kared et al., 2021) |
| SAKNRARTV | pp1ab | 4941 | 4949 | C*06:02 | multimer staining | (Saini et al., 2021) |
| SAKSASVYY | pp1ab | 2553 | 2561 | B*57:01 | AIM | (Tarke et al., 2021) |
| SALNHTKKW | pp1ab | 1648 | 1656 | B*57:01 | AIM | (Tarke et al., 2021) |
| SALWEIQQVV | pp1ab | 4093 | 4102 | A*02:01 | multimer staining/ICS | (Saini et al., 2021) |
| SAMVRMYIF | pp1ab | 2378 | 2386 | B*08:01 | multimer staining | (Saini et al., 2021) |
| SDGTGTIY | pp1ab | 4199 | 4206 | A*01:01 | multimer staining | (Saini et al., 2021) |
| SEDAQGMDNL | pp1ab | 2030 | 2039 | B*40:01 | AIM | (Tarke et al., 2021) |
| SAPPAQYEL | pp1ab | 1808 | 1816 | C*07:01 | multimer staining | (Saini et al., 2021) |
| SEFSSLPSY | pp1ab | 3946 | 3954 | B*44:03/A*02:01/B*07:02/B*44:10 | ICS/multimer staining/AIM | (Weingarten-Gabbay et al., 2021; Wagner et al., 2022; Schulien et al., 2021) |
| SEIIGYKAI | pp1ab | 2804 | 2812 | B*40:01 | AIM | (Tarke et al., 2021) |
| SEISMDNSPNL | pp1ab | 4112 | 4122 | HLA class I | ELISA/HTMA | (Snyder et al., 2020; Titov et al., 2022) |
| SELLTPLGI | pp1ab | 887 | 895 | B*40:01 | AIM | (Tarke et al., 2021) |
| SEVGPEHSLAEY | pp1ab | 376 | 387 | HLA class I | HTMA | (Snyder et al., 2020) |
| SEYKGPITDVFY | pp1ab | 1857 | 1868 | B*44:02 | AIM | (Tarke et al., 2021) |
| SEYTGNYQCGHY | pp1ab | 1825 | 1836 | B*44:02 | AIM | (Tarke et al., 2021) |
| SFGPLVRKI | pp1ab | 4717 | 4725 | A*24:02 | multimer staining | (Saini et al., 2021) |
| SFLPGVYSV | pp1ab | 3099 | 3107 | A*24:02 | multimer staining | (Saini et al., 2021) |
| SFYYVWKSY | pp1ab | 2389 | 2397 | A*29:02 | AIM | (Tarke et al., 2021) |
| SICSTMTNR | pp1ab | 4953 | 4961 | A*33:01 | AIM | (Tarke et al., 2021) |
| SIIQFPNTY | pp1ab | 2960 | 2968 | B*35:01 | AIM | (Tarke et al., 2021) |
| SLAIDAYPL | pp1ab | 5253 | 5261 | A*02:01 | proliferation | (Jin et al., 2021) |
| SLDNVLSTF | pp1ab | 2625 | 2633 | A*32:01 | AIM | (Tarke et al., 2021) |
| SLDTYPSLETI | pp1ab | 2297 | 2307 | A*02:01 | multimer staining | (Saini et al., 2021) |
| SLENVAFNV | pp1ab | 6453 | 6461 | A*02:01 | multimer staining | (Saini et al., 2021) |
| SLINTLNDL | pp1ab | 1433 | 1441 | A*02:01 | multimer staining | (Saini et al., 2021) |
| SLIYSTAAL | pp1ab | 2242 | 2250 | A*02:01 | AIM | (Tarke et al., 2021) |
| SLLMPILTL | pp1ab | 4631 | 4639 | A*02:01 | multimer staining | (Saini et al., 2021) |
| SLLSVLLSM | pp1ab | 3913 | 3921 | A*02:01 | multimer staining | (Saini et al., 2021) |
| SLPGVFCGV | pp1ab | 3013 | 3021 | A*02:01 | ELISPOT/multimer staining | (Saini et al., 2021; Prakash et al., 2021) |
| SLRPDTRYVL | pp1ab | 2947 | 2956 | C*07:02 | multimer staining | (Saini et al., 2021) |
| SLSGFKLKDCV | pp1ab | 3673 | 3683 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| SLYVNKHAF | pp1ab | 6343 | 6351 | B*08:01 | multimer staining | (Saini et al., 2021) |
| SMWALIISV | pp1ab | 3732 | 3740 | A*02:01 | ELISPOT/multimer staining/ICS | (Saini et al., 2021; Habel et al., 2020; Prakash et al., 2021) |
| SNEKQEILGTVSWNL | pp1ab | 1361 | 1375 | HLA class I | HTMA | (Snyder et al., 2020) |
| SNSGSDVLY | pp1ab | 3242 | 3250 | A*01:01 | multimer staining | (Saini et al., 2021) |
| SPSGVYQCAM | pp1ab | 3384 | 3393 | B*07:02 | multimer staining | (Saini et al., 2021) |
| SRVLGLKTL | pp1ab | 2114 | 2122 | C*07:01 | multimer staining | (Saini et al., 2021) |
| SRYWEPEF | pp1ab | 5305 | 5312 | C*07:01 | multimer staining | (Saini et al., 2021) |
| SSAKSASVY | pp1ab | 2552 | 2560 | B*15:01 | AIM | (Tarke et al., 2021) |
| SSEAFLIGCNY | pp1ab | 6999 | 7009 | A*01:01 | multimer staining | (Saini et al., 2021) |
| SSNVANYQK | pp1ab | 5587 | 5595 | HLA class I | HTMA | (Snyder et al., 2020) |
| SSTFNVPMEKLK | pp1ab | 2599 | 2610 | HLA class I | HTMA | (Snyder et al., 2020) |
| STAALGVLM | pp1ab | 2246 | 2254 | A*26:01 | AIM | (Tarke et al., 2021) |
| STFNVPMEK | pp1ab | 2600 | 2608 | A*11:01 | ICS/multimer staining | (Wagner et al., 2022; Schulien et al., 2021; Kared et al., 2021) |
| STNVTIATY | pp1ab | 2273 | 2281 | A*01:01/A*32:01 | AIM | (Tarke et al., 2021) |
| STSAFVETV | pp1ab | 483 | 491 | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| STVFPPTSF | pp1ab | 4710 | 4718 | B*57:01 | AIM | (Tarke et al., 2021) |
| SVPWDTIANY | pp1ab | 2132 | 2141 | A*26:01 | AIM | (Tarke et al., 2021) |
| SVVSKVVKV | pp1ab | 6764 | 6772 | A*02:01 | multimer staining | (Saini et al., 2021) |
| SVYYTSNPTTF | pp1ab | 1534 | 1544 | A*24:02 | multimer staining | (Saini et al., 2021) |
| SYATHSDKF | pp1ab | 6294 | 6302 | A*24:02 | multimer staining | (Saini et al., 2021) |
| SYFVVKRHTF | pp1ab | 4460 | 4469 | A*24:02 | ICS | (Jin et al., 2021) |
| SYSLFDMSKF | pp1ab | 7039 | 7048 | A*24:02 | multimer staining | (Saini et al., 2021) |
| SYYSLLMPI | pp1ab | 4628 | 4636 | A*24:02 | ICS | (Jin et al., 2021) |
| TANPKTPKY | pp1ab | 3356 | 3364 | C*07:01 | multimer staining | (Saini et al., 2021) |
| TDLEGNFY | pp1ab | 3438 | 3445 | A*01:01 | multimer staining | (Saini et al., 2021) |
| TDNYITTY | pp1ab | 1322 | 1329 | A*01:01 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| TEIDPKLDNYY | pp1ab | 1890 | 1900 | B*44:02/A*01:01 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| TETDLTKGPHEF | pp1ab | 5193 | 5204 | B*44:02 | AIM | (Tarke et al., 2021) |
| TEVVGDIIL | pp1ab | 2069 | 2077 | B*40:01 | ICS | (Schulien et al., 2021) |
| TFISAARQGF | pp1ab | 2632 | 2641 | A*24:02 | multimer staining | (Saini et al., 2021) |
| TFNGECPNF | pp1ab | 265 | 273 | A*24:02 | multimer staining | (Saini et al., 2021) |
| TFTYASALW | pp1ab | 4088 | 4096 | A*24:02 | multimer staining | (Saini et al., 2021) |
| TFYLTNDVSFL | pp1ab | 3113 | 3123 | HLA class I | HTMA | (Snyder et al., 2020) |
| TICAPLTVF | pp1ab | 6566 | 6574 | B*15:01 | multimer staining | (Saini et al., 2021) |
| TIEVNSFSGY | pp1ab | 1022 | 1031 | A*01:01 | multimer staining | (Saini et al., 2021) |
| TIIQTIVEV | pp1ab | 1000 | 1008 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| TISLAGSYK | pp1ab | 1504 | 1512 | A*68:01/A*03:01/A*11:01 | AIM/multimer staining | (Tarke et al., 2021; Kared et al., 2021) |
| TITQMNLKY | pp1ab | 4930 | 4938 | A*01:01 | multimer staining | (Saini et al., 2021) |
| TIWFLLLSV | pp1ab | 2230 | 2238 | A*02:01/A*02:07 | ICS/multimer staining | (Zhang et al., 2021; Xiao et al., 2022) |
| TLGVYDYLVST | pp1ab | 3807 | 3817 | HLA class I | HTMA | (Snyder et al., 2020) |
| TLIGDCATV | pp1ab | 6908 | 6916 | HLA class I | HTMA | (Snyder et al., 2020) |
| TLKEILVTY | pp1ab | 4533 | 4541 | A*29:02 | AIM | (Tarke et al., 2021) |
| TLMNVLTLV | pp1ab | 3710 | 3718 | A*02:01 | ICS | (Habel et al., 2020) |
| TLVPQEHYV | pp1ab | 5563 | 5571 | A*02:01 | HTMA/multimer staining/cytotoxicity/ICS/AIM | (Snyder et al., 2020; Pan et al., 2021) |
| TMADLVYAL | pp1ab | 4515 | 4523 | A*02:01 | ICS/AIM/multimer staining | (Saini et al., 2021; Habel et al., 2020; Quiros-Fernandez et al., 2021) |
| TNVLEGSVAY | pp1ab | 2936 | 2945 | B*35:01 | AIM | (Tarke et al., 2021) |
| TPHTVLQAV | pp1ab | 5318 | 5326 | B*51:01 | AIM | (Tarke et al., 2021) |
| TPKYKFVRI | pp1ab | 3361 | 3369 | B*08:01 | ELISPOT | (Nelde et al., 2021) |
| TPRDLGACI | pp1ab | 2684 | 2692 | B*07:02 | multimer staining | (Saini et al., 2021) |
| TPSKLIEY | pp1ab | 2898 | 2905 | B*35:01 | AIM | (Tarke et al., 2021) |
| TPVVQTIEV | pp1ab | 1017 | 1025 | B*07:02 | multimer staining | (Saini et al., 2021) |
| TSDLATNNLVVMAY | pp1ab | 587 | 600 | HLA class I | HTMA | (Snyder et al., 2020) |
| TSEDMLNPNY | pp1ab | 3308 | 3317 | A*01:01 | multimer staining | (Saini et al., 2021) |
| TSFGPLVRK | pp1ab | 4716 | 4724 | A*03:01 | multimer staining | (Kared et al., 2021) |
| TSLSGFKLKDCV | pp1ab | 3672 | 3683 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| TSNPTTFHL | pp1ab | 1538 | 1546 | B*57:01 | AIM | (Tarke et al., 2021) |
| TSSGDATTAY | pp1ab | 5072 | 5081 | A*01:01 | multimer staining | (Saini et al., 2021) |
| TTDPSFLGRY | pp1ab | 1637 | 1646 | A*01:01 | AIM/multimer staining/ICS/ELISA/ELISPOT/cytotoxicity | (Saini et al., 2021; Tarke et al., 2021; Titov et al., 2022; Ferretti et al., 2020; Nelde et al., 2021; Gangaev et al., 2021; Minervina et al., 2022) |
| TTDPSFLGRYM | pp1ab | 1637 | 1647 | A*01:01 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| TTIAKNTVK | pp1ab | 2196 | 2204 | A*30:01 | AIM | (Tarke et al., 2021) |
| TTIQTIVEV | pp1ab | 1000 | 1008 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| TTLPVNVAF | pp1ab | 6499 | 6507 | HLA class I | HTMA | (Snyder et al., 2020) |
| TTYPGQGLNGY | pp1ab | 1327 | 1337 | A*01:01 | multimer staining | (Saini et al., 2021) |
| TVKNGSIHLY | pp1ab | 2495 | 2504 | A*26:01 | AIM | (Tarke et al., 2021) |
| TVKPGNFNK | pp1ab | 4801 | 4809 | A*11:01 | proliferation | (Jin et al., 2021) |
| TVLSFCAFAV | pp1ab | 4265 | 4274 | HLA class I | HTMA | (Snyder et al., 2020) |
| TVYEKLKPV | pp1ab | 619 | 627 | A*02:01 | multimer staining | (Saini et al., 2021) |
| TYACWHHSI | pp1ab | 6148 | 6156 | A*24:02 | multimer staining | (Saini et al., 2021; Kared et al., 2021) |
| TYERHSLSHF | pp1ab | 2512 | 2521 | A*24:02 | multimer staining | (Saini et al., 2021) |
| TYKNTCDGTTF | pp1ab | 4079 | 4089 | A*24:02 | multimer staining | (Saini et al., 2021) |
| VAKSHNIAL | pp1ab | 2703 | 2711 | B*07:02 | multimer staining | (Saini et al., 2021) |
| VAMPNLYKM | pp1ab | 6807 | 6815 | B*57:01 | AIM | (Tarke et al., 2021) |
| VARDLSLQF | pp1ab | 2469 | 2477 | B*57:01 | AIM | (Tarke et al., 2021) |
| VELGTEVNEF | pp1ab | 862 | 871 | B*44:02 | AIM | (Tarke et al., 2021) |
| VENMTPRDL | pp1ab | 2680 | 2688 | B*44:03 | AIM | (Tarke et al., 2021) |
| VENPDILRV | pp1ab | 4558 | 4566 | B*44:03 | AIM | (Tarke et al., 2021) |
| VENPDILRVY | pp1ab | 4558 | 4567 | B*44:02 | AIM | (Tarke et al., 2021) |
| VENPHLMGWD | pp1ab | 5001 | 5010 | B*44:02 | AIM/multimer staining | (Tarke et al., 2021; Minervina et al., 2022) |
| VEVQPQLEM | pp1ab | 1006 | 1014 | B*40:01 | AIM | (Tarke et al., 2021) |
| VKNGSIHLY | pp1ab | 2496 | 2504 | C*06:02 | multimer staining | (Saini et al., 2021) |
| VLAAECTIF | pp1ab | 2914 | 2922 | B*15:01 | multimer staining | (Saini et al., 2021) |
| VLAWLYAAV | pp1ab | 3467 | 3475 | HLA class I | HTMA | (Snyder et al., 2020) |
| VLNEKCSAY | pp1ab | 852 | 860 | B*15:01 | multimer staining | (Saini et al., 2021) |
| VLQAVGACV | pp1ab | 5322 | 5330 | HLA class I | HTMA | (Snyder et al., 2020) |
| VLSEARQHL | pp1ab | 38 | 46 | A*02:01 | multimer staining | (Saini et al., 2021) |
| VLWAHGFEL | pp1ab | 6109 | 6117 | HLA class I | HTMA | (Snyder et al., 2020) |
| VMCGGSLYV | pp1ab | 5059 | 5067 | A*02:01 | ICS | (Jin et al., 2021) |
| VMVELVAEL | pp1ab | 84 | 92 | A*02:01 | ELISPOT/ICS/AIM | (Quiros-Fernandez et al., 2021; Prakash et al., 2021) |
| VMYASAVVLL | pp1ab | 3683 | 3692 | A*24:02 | multimer staining | (Saini et al., 2021) |
| VMYMGTLSY | pp1ab | 1768 | 1776 | A*03:01 | AIM | (Tarke et al., 2021) |
| VNRFNVAITRAKVGI | pp1ab | 558 | 572 | HLA class I | ICS/AIM | (Eggenhuizen et al., 2021) |
| VPANSTVL | pp1ab | 4260 | 4267 | B*07:02 | multimer staining | (Saini et al., 2021) |
| VPANSTVLSF | pp1ab | 4260 | 4269 | B*07:02 | multimer staining | (Saini et al., 2021) |
| VPFWITIAY | pp1ab | 3136 | 3144 | B*35:01 | AIM/ICS | (Tarke et al., 2021; Wagner et al., 2022) |
| VPGLPGTIL | pp1ab | 2866 | 2874 | B*07:02 | multimer staining | (Saini et al., 2021) |
| VPHISRQRL | pp1ab | 4503 | 4511 | B*07:02 | AIM | (Tarke et al., 2021) |
| VPHVGEIPV | pp1ab | 108 | 116 | B*07:02 | multimer staining | (Saini et al., 2021) |
| VPMEKLKTL | pp1ab | 2604 | 2612 | B*51:01 | AIM | (Tarke et al., 2021) |
| VPQEHYVRI | pp1ab | 5565 | 5573 | B*08:01 | multimer staining | (Saini et al., 2021) |
| VQSTQWSLF | pp1ab | 3595 | 3603 | A*24:02 | multimer staining | (Gangaev et al., 2021) |
| VRETMSYLF | pp1ab | 1728 | 1736 | C*07:01 | multimer staining | (Saini et al., 2021) |
| VRIQPGQTF | pp1ab | 3367 | 3375 | C*07:01 | multimer staining | (Saini et al., 2021) |
| VRNLQHRLY | pp1ab | 5112 | 5120 | C*07:01 | multimer staining | (Saini et al., 2021) |
| VRQALLKTV | pp1ab | 4574 | 4582 | C*06:02 | multimer staining | (Saini et al., 2021) |
| VRSIFSRTL | pp1ab | 544 | 552 | C*06:02 | multimer staining | (Saini et al., 2021) |
| VSALVYDNKLKAHKD | pp1ab | 452 | 466 | HLA class I | ICS/AIM | (Eggenhuizen et al., 2021) |
| VSSPDAVTAY | pp1ab | 1477 | 1486 | B*57:01/A*01:01 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| VTDTPKGPK | pp1ab | 4216 | 4224 | A*11:01 | ELISA/cytotoxicity | (Ferretti et al., 2020) |
| VTVKNGSIHLY | pp1ab | 2494 | 2504 | A*01:01 | AIM | (Tarke et al., 2021) |
| VVAIDYKHY | pp1ab | 1967 | 1975 | B*15:01 | AIM | (Tarke et al., 2021) |
| VVDKYFDCY | pp1ab | 4867 | 4875 | HLA class I | HTMA | (Snyder et al., 2020) |
| VVDYGARFY | pp1ab | 1415 | 1423 | A*01:01 | AIM | (Tarke et al., 2021) |
| VVNARLRAK | pp1ab | 5710 | 5718 | A*11:01 | multimer staining | (Kared et al., 2021) |
| VVQQLPETY | pp1ab | 6637 | 6645 | B*15:01 | multimer staining | (Saini et al., 2021) |
| VVSTGYHFR | pp1ab | 4733 | 4741 | A*11:01 | AIM/proliferation | (Tarke et al., 2021; Jin et al., 2021) |
| VVTTKIALK | pp1ab | 2753 | 2761 | A*03:01 | AIM | (Tarke et al., 2021) |
| VVVNAANVY | pp1ab | 1056 | 1064 | B*35:01 | AIM | (Tarke et al., 2021) |
| VVYRAFDIY | pp1ab | 4422 | 4430 | B*15:01 | multimer staining | (Saini et al., 2021) |
| VVYRGTTTY | pp1ab | 5533 | 5541 | HLA class I | HTMA | (Snyder et al., 2020) |
| VVYRGTTTYK | pp1ab | 5533 | 5542 | A*11:01/A*03:01 | ICS/multimer staining | (Schulien et al., 2021; Kared et al., 2021) |
| VYIGDPAQL | pp1ab | 5721 | 5729 | A*24:02/C*07:01 | ELISA/multimer staining/ICS/AIM/ELISPOT/cytotoxicity | (Saini et al., 2021; Wagner et al., 2022; Titov et al., 2022; Ferretti et al., 2020; Nelde et al., 2021; Kared et al., 2021; Minervina et al., 2022; Pan et al., 2021) |
| VYLPYPDPSRI | pp1ab | 5219 | 5229 | B*51:01 | AIM | (Tarke et al., 2021) |
| VYMPASWVM | pp1ab | 3653 | 3661 | A*24:02 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| VYRGTTTYKL | pp1ab | 5534 | 5543 | A*24:02 | multimer staining | (Saini et al., 2021) |
| WEPEFYEAM | pp1ab | 5308 | 5316 | B*40:01 | AIM | (Tarke et al., 2021) |
| WFFSNYLKR | pp1ab | 3155 | 3163 | A*31:01 | AIM | (Tarke et al., 2021) |
| WKYPQVNGL | pp1ab | 1656 | 1664 | C*07:01 | multimer staining | (Saini et al., 2021) |
| WLDMVDTSL | pp1ab | 3666 | 3674 | A*02:01 | AIM | (Tarke et al., 2021) |
| WLMWLIINL | pp1ab | 2363 | 2371 | A*02:01 | ELISPOT | (Prakash et al., 2021) |
| WRNTNPIQL | pp1ab | 7029 | 7037 | C*07:01 | multimer staining | (Saini et al., 2021) |
| WVLNNDYYR | pp1ab | 3004 | 3012 | A*31:01 | AIM | (Tarke et al., 2021) |
| YADVFHLYL | pp1ab | 5269 | 5277 | C*07:02 | multimer staining | (Saini et al., 2021) |
| YAFEHIVY | pp1ab | 6682 | 6689 | B*35:01 | ICS | (Swaminathan et al., 2022) |
| YAISAKNRAR | pp1ab | 4938 | 4947 | A*68:01 | AIM | (Tarke et al., 2021) |
| YAKPFLNKV | pp1ab | 2141 | 2149 | C*06:02 | multimer staining | (Saini et al., 2021) |
| YASAVVLLI | pp1ab | 3685 | 3693 | C*06:02 | multimer staining | (Saini et al., 2021) |
| YAYLRKHF | pp1ab | 5138 | 5145 | B*08:01 | multimer staining | (Saini et al., 2021) |
| YDYLVSTQEF | pp1ab | 3811 | 3820 | C*07:02 | multimer staining | (Saini et al., 2021) |
| YEKLKPVL | pp1ab | 621 | 628 | B*08:01 | multimer staining | (Saini et al., 2021) |
| YENFNQHEV | pp1ab | 1135 | 1143 | B*40:01 | AIM | (Tarke et al., 2021) |
| YERHSLSHF | pp1ab | 2513 | 2521 | B*44:02 | AIM | (Tarke et al., 2021) |
| YFDKAGQKTY | pp1ab | 2504 | 2513 | C*07:02 | multimer staining | (Saini et al., 2021) |
| YFIKGLNNL | pp1ab | 4229 | 4237 | C*07:02 | multimer staining | (Saini et al., 2021) |
| YFMRFRRAF | pp1ab | 3063 | 3071 | A*24:02 | multimer staining | (Saini et al., 2021) |
| YFVVKRHTF | pp1ab | 4461 | 4469 | B*08:01/A*24:02 | multimer staining | (Saini et al., 2021) |
| YIATNGPLK | pp1ab | 1090 | 1098 | A*11:01 | AIM | (Tarke et al., 2021) |
| YIFFASFYY | pp1ab | 2384 | 2392 | A*29:02 | AIM/HTMA | (Snyder et al., 2020; Tarke et al., 2021) |
| YKIEELFYSY | pp1ab | 6286 | 6295 | A*01:01 | multimer staining | (Saini et al., 2021) |
| YLASGGQPI | pp1ab | 4283 | 4291 | A*02:01 | ELISPOT | (Prakash et al., 2021) |
| YLATALLTL | pp1ab | 1675 | 1683 | A*02:01 | AIM/ELISPOT/ICS/multimer staining | (Saini et al., 2021; Tarke et al., 2021; Kared et al., 2021; Quiros-Fernandez et al., 2021; Prakash et al., 2021) |
| YLDAYNMMI | pp1ab | 6419 | 6427 | A*02:01 | ELISPOT/HTMA/multimer staining | (Snyder et al., 2020; Kared et al., 2021; Prakash et al., 2021) |
| YLFDESGEF | pp1ab | 906 | 914 | B*15:01 | multimer staining | (Saini et al., 2021) |
| YLFDESGEFKL | pp1ab | 906 | 916 | A*02:01 | ELISA/multimer staining/cytotoxicity | (Titov et al., 2022; Ferretti et al., 2020) |
| YLITPVHV | pp1ab | 2788 | 2795 | A*02:01 | AIM | (Tarke et al., 2021) |
| YLITPVHVM | pp1ab | 2788 | 2796 | B*15:01/A*02:01/C*07:01 | multimer staining | (Saini et al., 2021) |
| YLKLTDNVY | pp1ab | 1031 | 1039 | B*15:01 | multimer staining | (Saini et al., 2021) |
| YLKLTDNVYIK | pp1ab | 1031 | 1041 | HLA class I | HTMA | (Snyder et al., 2020) |
| YLKRRVVF | pp1ab | 3160 | 3167 | B*08:01 | multimer staining | (Saini et al., 2021) |
| YLNSTNVTI | pp1ab | 2270 | 2278 | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| YLNTLTLAV | pp1ab | 6851 | 6859 | HLA class I | HTMA | (Snyder et al., 2020) |
| YLPYPDPSRI | pp1ab | 5220 | 5229 | B*51:01/A*02:07 | AIM/ICS | (Tarke et al., 2021; Jin et al., 2021) |
| YLPYPDPSRIL | pp1ab | 5220 | 5230 | A*24:02 | multimer staining | (Saini et al., 2021) |
| YLTNDVSFLA | pp1ab | 3115 | 3124 | A*02:01 | AIM | (Tarke et al., 2021)??? |
| YLYFIKGLNNL | pp1ab | 4227 | 4237 | A*02:01 | multimer staining | (Saini et al., 2021) |
| YMHHMELPTGV | pp1ab | 3424 | 3434 | A*02:01 | multimer staining | (Saini et al., 2021) |
| YMSALNHTK | pp1ab | 1646 | 1654 | A*03:01 | AIM | (Tarke et al., 2021) |
| YNLWNTFTRL | pp1ab | 6442 | 6451 | A*02:01 | multimer staining | (Saini et al., 2021) |
| YPQVNGLTSI | pp1ab | 1658 | 1667 | B*51:01 | AIM | (Tarke et al., 2021) |
| YQKVGMQKY | pp1ab | 5593 | 5601 | HLA class I | HTMA | (Snyder et al., 2020) |
| YRGTTTYKL | pp1ab | 5535 | 5543 | C*06:02 | multimer staining | (Saini et al., 2021) |
| YRSLPGVF | pp1ab | 3011 | 3018 | C*07:01 | multimer staining | (Saini et al., 2021) |
| YRYNLPTM | pp1ab | 4848 | 4855 | C*07:02 | multimer staining | (Saini et al., 2021) |
| YRYNLPTMC | pp1ab | 4848 | 4856 | C*06:02 | multimer staining | (Saini et al., 2021) |
| YSDVENPHLMGW | pp1ab | 4998 | 5009 | B*44:02 | AIM | (Tarke et al., 2021) |
| YTELEPPCRF | pp1ab | 4206 | 4215 | A*01:01 | multimer staining | (Saini et al., 2021) |
| YTGNYQCGHY | pp1ab | 1827 | 1836 | A*01:01 | multimer staining | (Saini et al., 2021) |
| YTMADLVYAL | pp1ab | 4514 | 4523 | HLA class I | HTMA | (Snyder et al., 2020) |
| YTTTIKPVTY | pp1ab | 1873 | 1882 | A*26:01/A*01:01 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| YVFCTVNAL | pp1ab | 5679 | 5687 | HLA class I | HTMA | (Snyder et al., 2020) |
| YVMHANYIF | pp1ab | 7020 | 7028 | A*32:01/A*26:01 | AIM | (Tarke et al., 2021) |
| YVYANGGKGF | pp1ab | 2435 | 2444 | A*26:01/B*15:01 | AIM | (Tarke et al., 2021) |
| YVYLPYPDPSRILGA | pp1ab | 5218 | 5232 | B*51:01 | ELISPOT/ICS | (Swadling et al., 2022) |
| YYKKDNSY | pp1ab | 1899 | 1906 | C*07:02 | multimer staining | (Saini et al., 2021) |
| YYKKDNSYF | pp1ab | 1899 | 1907 | A*24:02 | AIM | (Tarke et al., 2021) |
| YYPSARIVY | pp1ab | 5622 | 5630 | A*24:02 | multimer staining | (Saini et al., 2021) |
| YYRARAGEAANF | pp1ab | 1699 | 1710 | HLA class I | HTMA | (Snyder et al., 2020) |
| YYTSNPTTF | pp1ab | 1536 | 1544 | A*24:02 | multimer staining/ICS | (Saini et al., 2021; Kared et al., 2021) |
| YYTSNPTTFHL | pp1ab | 1536 | 1546 | A*24:02 | multimer staining | (Saini et al., 2021) |
| VTNNTFTLK | pp1ab | 808 | 816 | A*03:01/A*11:01 | ICS/multimer staining/cytotoxicity/ELISA | (Wagner et al., 2022; Ferretti et al., 2020; Kared et al., 2021) |
| ADAGFIKQY | S | 829 | 837 | B*44:03/B*44:02 | ELISA | (Titov et al., 2022) |
| AEHVNNSY | S | 653 | 660 | B*44:03/B*44:02 | AIM | (Tarke et al., 2021) |
| AEIRASANL | S | 1016 | 1024 | B*44:02/B*44:03/B*40:01 | AIM | (Tarke et al., 2021) |
| AEIRASANLAATK | S | 1016 | 1028 | HLA class I | HTMA | (Snyder et al., 2020) |
| AEVQIDRL | S | 989 | 996 | B*40:01/B*44:03/B*44:02 | AIM | (Tarke et al., 2021) |
| AEVQIDRLI | S | 989 | 997 | B*44:03/B*44:02 | AIM/multimer staining | (Tarke et al., 2021; Minervina et al., 2022) |
| AGFIKQYGDCLGDIA | S | 831 | 845 | HLA class I | ICS | (Zhang et al., 2022) |
| AHFPREGVF | S | 1087 | 1095 | B*39:01 | AIM | (Tarke et al., 2022) |
| AIPINFTISV | S | 710 | 719 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| AIPTNFTISV | S | 713 | 722 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| ALDPLSETK | S | 292 | 300 | A*03:01 | AIM | (Tarke et al., 2021) |
| ALNTLVKQL | S | 958 | 966 | A*02:01 | ELISPOT/multimer staining/AIM/ICS | (Wagner et al., 2022; Hu et al., 2022; Prakash et al., 2021) |
| APHGVVFL | S | 1056 | 1063 | B*07:02 | multimer staining | (Kared et al., 2021) |
| APHGVVFLHV | S | 1056 | 1065 | B*07:02 | multimer staining | (Saini et al., 2021) |
| APHGVVFLHVTYV | S | 1056 | 1068 | HLA class I | HTMA | (Snyder et al., 2020) |
| AQALNTLVKQL | S | 956 | 966 | HLA class I | HTMA | (Snyder et al., 2020) |
| ASANLAATK | S | 1020 | 1028 | A*11:01 | ICS | (Jin et al., 2021) |
| ASVYAWNRK | S | 348 | 356 | A*30:01 | ICS | (Jin et al., 2021) |
| AYSNNSIAI | S | 706 | 714 | A*24:02 | AIM | (Tarke et al., 2021) |
| CALDPLSETK | S | 291 | 300 | HLA class I | HTMA | (Snyder et al., 2020) |
| CEFQFCNDPFLGVYY | S | 131 | 145 | HLA class I | ICS | (Zhang et al., 2022) |
| CFTNVYADSF | S | 391 | 400 | A*24:02 | ICS | (Jin et al., 2021) |
| CMTSCCSCLK | S | 1236 | 1245 | HLA class I | HTMA | (Snyder et al., 2020) |
| CNDPFLGVY | S | 136 | 144 | A*01:01/A*02:01 | multimer staining | (Saini et al., 2021; Xiao et al., 2022) |
| CNDPFLGVYY | S | 136 | 145 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| CTFEYVSQPFLM | S | 166 | 177 | HLA class I | HTMA | (Snyder et al., 2020) |
| CTFEYVSQPFLMDLE | S | 175 | 189 | C*07:02 | ELISPOT | (Peng et al., 2020) |
| CTLKSFTVEK | S | 301 | 310 | A*11:01 | ICS | (Jin et al., 2021) |
| CVADYSVLY | S | 361 | 369 | A*29:02/A*26:01/A*01:01/B*15:01 | AIM/ICS/multimer staining | (Saini et al., 2021; Tarke et al., 2021; Wagner et al., 2022) |
| DAVRDPQTL | S | 574 | 582 | B*51:01 | AIM | (Tarke et al., 2021) |
| DGVYFASTEK | S | 88 | 97 | A*68:01 | AIM | (Tarke et al., 2021) |
| DLPIGINITRFQTL | S | 228 | 241 | HLA class I | HTMA | (Snyder et al., 2020) |
| DSFKEELDKY | S | 1146 | 1155 | HLA class I | HTMA | (Snyder et al., 2020) |
| DSKVGGNYNY | S | 442 | 451 | A*26:01 | AIM | (Tarke et al., 2021) |
| EILDITPCSF | S | 583 | 592 | A*26:01/A*02:01/B*07:02 | AIM/multimer staining/HTMA | (Tarke et al., 2021; Weingarten-Gabbay et al., 2021) |
| EILDITPCSFG | S | 583 | 593 | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| EILPVSMTK | S | 725 | 733 | A*03:01/A*68:01 | AIM | (Tarke et al., 2021) |
| EIYQAGSTPCNGVEG | S | 471 | 485 | HLA class I | ICS | (Zhang et al., 2022) |
| ELDSFKEEL | S | 1144 | 1152 | A*02:01 | AIM | (Tarke et al., 2022) |
| ELLHAPATV | S | 516 | 524 | A*02:01 | multimer staining | (Saini et al., 2021) |
| EPLVDLPI | S | 224 | 231 | B*51:01 | AIM | (Tarke et al., 2021) |
| EPVLKGVKL | S | 1262 | 1270 | B*07:02 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| ETKCTLKSF | S | 298 | 306 | A*26:01 | AIM | (Tarke et al., 2021) |
| EVFAQVKQI | S | 780 | 788 | B*51:01 | AIM | (Tarke et al., 2021) |
| EVFAQVKQIY | S | 780 | 789 | A*26:01 | AIM | (Tarke et al., 2021) |
| EVFNATRFASVY | S | 340 | 351 | A*26:01 | AIM | (Tarke et al., 2021) |
| EYVSQPFLM | S | 169 | 177 | A*24:02 | AIM/ELISPOT | (Tarke et al., 2021; Hu et al., 2022) |
| FAMQMAYRF | S | 898 | 906 | B*35:01/B*51:01/B*57:03 | ELISPOT/AIM | (Tarke et al., 2021; Somogyi et al., 2021; Tarke et al., 2022) |
| FASTEKSNI | S | 92 | 100 | B*51:01 | AIM | (Tarke et al., 2022) |
| FASVYAWNR | S | 347 | 355 | A*68:01 | AIM | (Tarke et al., 2021) |
| FCNDPFLGV | S | 135 | 143 | A*02:01 | AIM | (Tarke et al., 2022) |
| FCNDPFLGVY | S | 135 | 144 | B*15:01/B*35:01/A*02:01 | ELISA/multimer staining | (Titov et al., 2022; Xiao et al., 2022) |
| FCNDPFLGVYY | S | 135 | 145 | A*01:01 | HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020) |
| FDEDDSEPVL | S | 1256 | 1265 | B*40:01 | AIM | (Tarke et al., 2021) |
| FDNPVLPFNDGVYF | S | 79 | 92 | B*35:01 | AIM | (Tarke et al., 2021) |
| FELLHAPATV | S | 515 | 524 | A*02:01 | multimer staining | (Saini et al., 2021) |
| FERDISTEI | S | 464 | 472 | B*40:01 | AIM | (Tarke et al., 2021) |
| FERDISTEIY | S | 464 | 473 | B*44:03/B*15:01 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| FEYVSQPFL | S | 168 | 176 | B*49:01 | ICS | (Swaminathan et al., 2022) |
| FEYVSQPFLM | S | 168 | 177 | B*40:01 | AIM | (Tarke et al., 2021) |
| FGEVFNATRFASVY | S | 338 | 351 | HLA class I | HTMA | (Snyder et al., 2020) |
| FIAGLIAIV | S | 1220 | 1228 | A*02:01 | ELISPOT/multimer staining/AIM/ICS/HTMA | (Saini et al., 2021; Snyder et al., 2020; Jin et al., 2021; Poran et al., 2020; Prakash et al., 2021) |
| FIEDLLFNK | S | 817 | 825 | A*11:01 | ICS/proliferation | (Jin et al., 2021) |
| FKIYSKHTPI | S | 201 | 210 | A*02:03 | proliferation | (Jin et al., 2021) |
| FKNLREFVF | S | 186 | 194 | C*07:01 | multimer staining | (Saini et al., 2021) |
| FLHVTYVPA | S | 1062 | 1070 | A*02:03 | multimer staining/proliferation/ICS | (Jin et al., 2021; Deng et al., 2021) |
| FLPFFSNV | S | 55 | 62 | A*02:01 | multimer staining | (Saini et al., 2021) |
| FLPFFSNVTW | S | 55 | 64 | B*53:01 | AIM | (Tarke et al., 2021) |
| FLPFFSNVTWFHAI | S | 55 | 68 | HLA class I | HTMA | (Snyder et al., 2020) |
| FPQSAPHGV | S | 1052 | 1060 | B*07:02/B*53:01 | AIM | (Tarke et al., 2021) |
| FPQSAPHGVVF | S | 1052 | 1062 | B*35:01/B*08:01 | AIM/HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020; Tarke et al., 2021) |
| FPREGVFV | S | 1089 | 1096 | B*51:01/B*07:02 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| FQFCNDPFL | S | 133 | 141 | A*02:01 | multimer staining | (Qiu et al., 2021) |
| FQPTNGVGY | S | 497 | 505 | B*15:01 | ELISA/HTMA | (Snyder et al., 2020; Titov et al., 2022) |
| FRSSVLHST | S | 43 | 51 | C*07:01 | multimer staining | (Saini et al., 2021) |
| FTISVTTEI | S | 718 | 726 | A*02:01/A*26:01/B*52:01 | multimer staining/AIM/ELISPOT | (Tarke et al., 2021; Hu et al., 2022; Tarke et al., 2022; Qiu et al., 2021) |
| FTISVTTEIL | S | 718 | 727 | HLA class I | HTMA | (Snyder et al., 2020) |
| FVFFVLLPLV | S | 2 | 11 | A*02:01 | multimer staining | (Qiu et al., 2021) |
| FVFKNIDGY | S | 192 | 200 | A*29:02/A*26:01 | AIM/HTMA | (Snyder et al., 2020; Tarke et al., 2021) |
| FVFLVLLPL | S | 2 | 10 | A*02:01 | ELISPOT | (Prakash et al., 2021) |
| FVFLVLLPLV | S | 2 | 11 | A*02:01 | multimer staining/proliferation | (Jin et al., 2021; Qiu et al., 2021) |
| FVIRGDEVR | S | 400 | 408 | A*68:01 | AIM | (Tarke et al., 2021) |
| FVSNGTHWF | S | 1095 | 1103 | A*26:01/B*35:01/C*12:03 | AIM | (Tarke et al., 2021; Tarke et al., 2022) |
| FVSNGTHWFV | S | 1095 | 1104 | A*02:03 | proliferation | (Jin et al., 2021) |
| GAAAYYVGY | S | 261 | 269 | A*29:02 | AIM | (Tarke et al., 2021) |
| GCVIAWNSNNLDSKV | S | 431 | 445 | HLA class I | ICS/AIM | (Mahajan et al., 2021) |
| GEVFNATRF | S | 339 | 347 | B*40:01/B*44:02/B*44:03 | AIM | (Tarke et al., 2021) |
| GGNYNYLYRLFRKSN | S | 446 | 460 | HLA class I | ICS/AIM | (Mahajan et al., 2021) |
| GIYQTSNFR | S | 311 | 319 | A*33:03 | ICS | (Jin et al., 2021) |
| GKLQDVVNQNAQALN | S | 946 | 960 | HLA class I | ICS/AIM | (Mahajan et al., 2021) |
| GKYEQYIKW | S | 1204 | 1212 | A*24:02 | ICS | (Shimizu et al., 2021) |
| GKYEQYIKWPWYIWL | S | 1204 | 1218 | A*24:02 | ICS | (Shimizu et al., 2021) |
| GLTVLPPLL | S | 857 | 865 | A*02:01 | AIM/multimer staining | (Tarke et al., 2021; Poran et al., 2020) |
| GNYNYLYRLF | S | 447 | 456 | A*24:02 | multimer staining | (Saini et al., 2021) |
| GPKKSTNLV | S | 526 | 534 | HLA class I | HTMA | (Snyder et al., 2020) |
| GPKKSTNLVKNKCVN | S | 535 | 549 | A*31:01 | ELISPOT | (Peng et al., 2020) |
| GRLQSLQTY | S | 999 | 1007 | B*27:05 | ELISA | (Titov et al., 2022) |
| GSFCTQLNR | S | 757 | 765 | HLA class I | HTMA | (Snyder et al., 2020) |
| GTHWFVTQR | S | 1099 | 1107 | A*31:01/A*68:01/A*11:01/B*57:01 | AIM/HTMA/multimer staining/ICS | (Snyder et al., 2020; Tarke et al., 2021; Jin et al., 2021; Kared et al., 2021; Tarke et al., 2022) |
| GTITSGWTF | S | 880 | 888 | A*24:02 | AIM/HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020; Tarke et al., 2021) |
| GVFVSNGTHW | S | 1093 | 1102 | B*57:01 | AIM | (Tarke et al., 2021) |
| GVVFLHVTY | S | 1059 | 1067 | A*32:01 | AIM | (Tarke et al., 2021) |
| GVYFASTEK | S | 89 | 97 | A*68:01/A*03:01/A*11:01 | AIM/ICS/multimer staining | (Tarke et al., 2021; Wagner et al., 2022; Jin et al., 2021; Kared et al., 2021) |
| GVYHKNNK | S | 140 | 147 | A*11:01 | ICS | (Zhang et al., 2021) |
| GVYYHKNNK | S | 142 | 150 | A*03:01/A*11:01 | ICS/AIM/multimer staining | (Zhang et al., 2021; Tarke et al., 2021; Jin et al., 2021) |
| GVYYPDKVF | S | 35 | 43 | A*32:01 | AIM | (Tarke et al., 2022) |
| GVYYPDKVFR | S | 35 | 44 | A*68:01/A*03:01 | AIM | (Tarke et al., 2021) |
| GWTAGAAAYYVGYLQ | S | 257 | 271 | HLA class I | ELISA | (Li et al., 2021) |
| GYLQPRTFL | S | 268 | 276 | A*24:02 | ELISPOT | (Hu et al., 2022) |
| GYLQPRTFLL | S | 268 | 277 | A*24:02 | AIM | (Tarke et al., 2021) |
| GYQPYRVVVLSF | S | 504 | 515 | HLA class I | HTMA | (Snyder et al., 2020) |
| HADQLTPTW | S | 625 | 633 | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| HLMSFPQSA | S | 1048 | 1056 | A*02:01 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| HVSGTNGTK | S | 69 | 77 | A*68:01 | AIM | (Tarke et al., 2021) |
| HVTYVPAQEK | S | 1064 | 1073 | A*68:01 | AIM | (Tarke et al., 2021) |
| HVTYVPAQEKNF | S | 1064 | 1075 | HLA class I | HTMA | (Snyder et al., 2020) |
| HWFVTQRNF | S | 1101 | 1109 | A*24:02 | AIM/ELISPOT | (Tarke et al., 2021; Hu et al., 2022) |
| IAIPTNFTI | S | 712 | 720 | B*53:01/B*51:01 | AIM | (Tarke et al., 2021) |
| IANQFNSAI | S | 923 | 931 | B*51:01/C*03:04 | AIM | (Tarke et al., 2021; Tarke et al., 2022) |
| IEDLLFNKV | S | 818 | 826 | B*52:01 | AIM | (Tarke et al., 2022) |
| IGAEHVNNSY | S | 651 | 660 | HLA class I | HTMA | (Snyder et al., 2020) |
| IGINITRFQTLLALH | S | 231 | 245 | HLA class I | ICS | (Zhang et al., 2022) |
| IITTDNTFV | S | 1114 | 1122 | A*02:01 | HTMA/multimer staining | (Snyder et al., 2020; Xiao et al., 2022) |
| IHADQLTPTW | S | 624 | 633 | B*53:01 | AIM | (Tarke et al., 2021) |
| IKWPWYIWL | S | 1210 | 1218 | A*24:02 | ICS | (Shimizu et al., 2021) |
| ILPDPSKPSK | S | 805 | 814 | HLA class I | HTMA | (Snyder et al., 2020) |
| INITRFQTL | S | 233 | 241 | B*08:01 | AIM | (Tarke et al., 2021) |
| IPFAMQMAY | S | 896 | 904 | B*35:01/B*51:01 | multimer staining/AIM/ICS | (Tarke et al., 2021; Swaminathan et al., 2022) |
| IPFAMQMAYRFNGIG | S | 896 | 910 | HLA class I | ICS/AIM | (Mahajan et al., 2021) |
| IPIGAGICASY | S | 664 | 674 | HLA class I | HTMA | (Snyder et al., 2020) |
| IPTNFTISV | S | 714 | 722 | B*07:02/B*51:01 | AIM/ multimer staining | (Tarke et al., 2021; Gangaev et al., 2021) |
| ISGINASVVNIQKEI | S | 1169 | 1183 | HLA class I | ICS | (Titov et al., 2022) |
| ITGRLQSLQTY | S | 997 | 1007 | A*01:01 | multimer staining | (Saini et al., 2021) |
| IWLGFIAGL | S | 1216 | 1224 | A*24:02 | ICS | (Shimizu et al., 2021) |
| IYKTPPIKDF | S | 788 | 797 | C*07:02/A*24:02 | multimer staining/ICS | (Saini et al., 2021; Jin et al., 2021) |
| IYQTSNFRV | S | 312 | 320 | A*24:02 | AIM/ELISPOT | (Tarke et al., 2021; Hu et al., 2022) |
| IYSKHTPINL | S | 203 | 212 | HLA class I | HTMA | (Snyder et al., 2020) |
| KCYGVSPTK | S | 378 | 386 | A*03:01/A*11:01 | AIM/ELISA/ICS/multimer staining/cytotoxicity | (Saini et al., 2021; Tarke et al., 2021; Wagner et al., 2022; Titov et al., 2022; Ferretti et al., 2020) |
| KEIDRLNEV | S | 1181 | 1189 | B*44:03/B*44:02/B*40:01 | AIM/HTMA | (Snyder et al., 2020; Tarke et al., 2021) |
| KFLPFQQFGR | S | 558 | 567 | A*31:01 | AIM | (Tarke et al., 2021) |
| KIADYNYKL | S | 417 | 425 | A*02:01 | ICS/ multimer staining/AIM/proliferation | (Zhang et al., 2021; Saini et al., 2021; Wagner et al., 2022; Chen et al., 2021) |
| KIYSKHTPI | S | 202 | 210 | B*08:01 | AIM | (Tarke et al., 2021) |
| KLNDLCFTNV | S | 386 | 395 | A*02:01 | ICS/multimer staining | (Jin et al., 2021; Poran et al., 2020) |
| KLPDDFTGCV | S | 424 | 433 | A*02:01 | HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020; Pan et al., 2021) |
| KNIDGYFKIY | S | 195 | 204 | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| KNLREFVFK | S | 187 | 195 | A*30:01 | ICS | (Jin et al., 2021) |
| KPFERDISTEI | S | 462 | 472 | B*07:02 | AIM | (Tarke et al., 2021) |
| KPFERDISTEIY | S | 462 | 473 | HLA class I | HTMA | (Snyder et al., 2020) |
| KQIYKTPPI | S | 786 | 794 | B*52:01 | AIM | (Tarke et al., 2022) |
| KQIYKTPPIKDF | S | 786 | 797 | HLA class I | HTMA | (Snyder et al., 2020) |
| KSFTVEKGI | S | 304 | 312 | B*52:01 | AIM | (Tarke et al., 2022) |
| KSNLKPFER | S | 458 | 466 | A*31:01 | AIM | (Tarke et al., 2021) |
| KSWMESEFRVY | S | 150 | 160 | HLA class I | HTMA | (Snyder et al., 2020) |
| KTSVDCTMYI | S | 733 | 742 | HLA class I | HTMA | (Snyder et al., 2020) |
| KVFRSSVLH | S | 41 | 49 | A*30:01/A*03:01 | AIM | (Tarke et al., 2021) |
| KVGGNYNYLY | S | 444 | 453 | A*29:02 | AIM | (Tarke et al., 2021) |
| KWPWYIWLG | S | 1211 | 1219 | A*24:02 | ICS | (Shimizu et al., 2021) |
| KWPWYIWLGF | S | 1211 | 1220 | A*24:02 | ICS | (Wagner et al., 2022; Schulien et al., 2021) |
| KYEQYIKWP | S | 1205 | 1213 | A*24:02 | ICS | (Shimizu et al., 2021) |
| KYEQYIKWPWYIWLG | S | 1205 | 1219 | HLA class I | ELISA | (Li et al., 2021) |
| LADAGFIKQY | S | 828 | 837 | A*01:01 | ELISA/multimer staining | (Saini et al., 2021; Titov et al., 2022) |
| LEPLVDLPI | S | 223 | 231 | HLA class I | HTMA | (Snyder et al., 2020) |
| LGAENSVAY | S | 699 | 707 | B*35:01/C*16:02 | AIM | (Tarke et al., 2021; Tarke et al., 2022) |
| LGAENSVAYSNN | S | 699 | 710 | HLA class I | HTMA | (Snyder et al., 2020) |
| LGFIAGLIA | S | 1218 | 1226 | A*24:02 | ICS | (Shimizu et al., 2021) |
| LITGRLQSLQTYV | S | 996 | 1008 | HLA class I | HTMA | (Snyder et al., 2020) |
| LLALHRSYL | S | 241 | 249 | HLA class I | HTMA | (Snyder et al., 2020) |
| LLFNKVTLA | S | 821 | 829 | A*02:01 | HTMA/multimer staining | (Snyder et al., 2020; Pan et al., 2021) |
| LLQYGSFCT | S | 753 | 761 | HLA class I | HTMA | (Snyder et al., 2020) |
| LPFNDGVYF | S | 84 | 92 | B*07:02/B*35:01/B*51:01 | AIM/ICS | (Tarke et al., 2021; Wagner et al., 2022) |
| LPIGINITRF | S | 229 | 238 | B*07:02/B*35:01 | AIM | (Tarke et al., 2021) |
| LPLVSSQCV | S | 8 | 16 | B*51:01 | AIM | (Tarke et al., 2021) |
| LPPAYTNSF | S | 24 | 32 | B*53:01/B*07:02/B*35:01 | AIM/HTMA | (Snyder et al., 2020; Tarke et al., 2021) |
| LPPLLTDEM | S | 861 | 869 | B*35:01/B*51:01 | AIM | (Tarke et al., 2021; Tarke et al., 2022) |
| LPQGFSAL | S | 216 | 223 | B*08:01/B*07:02 | AIM/HTMA/multimer staining | (Snyder et al., 2020; Tarke et al., 2021) |
| LPQGFSALEPL | S | 216 | 226 | B*07:02 | multimer staining | (Saini et al., 2021) |
| LQELGKYEQY | S | 1200 | 1209 | A*01:01 | multimer staining | (Saini et al., 2021) |
| LQELGKYEQYIKWPW | S | 1200 | 1214 | A*24:02 | ICS | (Shimizu et al., 2021) |
| LQIPFAMQM | S | 894 | 902 | HLA class I | ELISA | (Titov et al., 2022) |
| LQIPFAMQMAY | S | 894 | 904 | HLA class I | HTMA | (Snyder et al., 2020) |
| LQPELDSFKEELDKY | S | 1141 | 1155 | HLA class I | ELISA | (Li et al., 2021) |
| LQSYGFQPT | S | 492 | 500 | A*02:06 | proliferation | (Jin et al., 2021) |
| LQTYVTQQLIRAAEI | S | 1004 | 1018 | HLA class I | ELISA/ICS | (Titov et al., 2022) |
| LSSTASALGK | S | 938 | 947 | HLA class I | HTMA | (Snyder et al., 2020) |
| LLTDEMIAQY | S | 864 | 873 | A*01:01 | multimer staining | (Saini et al., 2021) |
| LTDEMIAQY | S | 865 | 873 | A*01:01/A*29:02/B*35:01/C*07:02 | ICS/AIM/multimer staining/ELISA/ELISPOT | (Saini et al., 2021; Tarke et al., 2021; Wagner et al., 2022; Titov et al., 2022; Schulien et al., 2021; Nelde et al., 2021; Kared et al., 2021; Gangaev et al., 2021; Minervina et al., 2022) |
| LTDEMIAQYT | S | 865 | 874 | A*01:01 | multimer staining | (Saini et al., 2021) |
| LVKNKCVNF | S | 533 | 541 | B*15:01 | multimer staining | (Saini et al., 2021) |
| LVKQLSSNF | S | 962 | 970 | A*32:01 | AIM | (Tarke et al., 2022) |
| LYNSASFSTF | S | 368 | 377 | A*24:02 | ICS | (Jin et al., 2021) |
| MIAQYTSAL | S | 869 | 877 | B*07:02/B*08:01/A*02:01 | AIM/multimer staining/ICS | (Saini et al., 2021; Tarke et al., 2021; Jin et al., 2021) |
| MTKTSVDCTMYICGD | S | 731 | 745 | HLA class I | ICS | (Zhang et al., 2022) |
| NASVVNIQK | S | 1173 | 1181 | A*68:01 | AIM | (Tarke et al., 2021) |
| NATNVVIKV | S | 122 | 130 | A*02:01/B*07:02/B*51:01/B*52:01/C*16:02 | multimer staining/AIM | (Weingarten-Gabbay et al., 2021; Tarke et al., 2022) |
| NATRFASVY | S | 343 | 351 | B*35:01 | AIM | (Tarke et al., 2021) |
| NCTFEYVSQPFLMDL | S | 165 | 179 | HLA class I | ELISPOT | (Zhao et al., 2021) |
| NESLIDLQEL | S | 1194 | 1203 | B*40:01 | AIM | (Tarke et al., 2021) |
| NFRVQPTESIVRFPN | S | 317 | 331 | A*25:02 | ELISPOT/AIM | (Zhao et al., 2021) |
| NGVEGFNCY | S | 481 | 489 | HLA class I | HTMA | (Snyder et al., 2020) |
| NGVEGFNCYFPLQSY | S | 481 | 495 | HLA class I | AIM | (Mahajan et al., 2021) |
| NGVGYQPYR | S | 501 | 509 | A*33:03 | ICS | (Jin et al., 2021) |
| NIADYNYKL | S | 414 | 422 | A*02:01 | ICS | (Zhang et al., 2021) |
| NITRFQTL | S | 234 | 241 | B*08:01 | AIM | (Tarke et al., 2021) |
| NKSWMESEFRVYSSA | S | 149 | 163 | HLA class I | ELISPOT | (Zhao et al., 2021) |
| NLDSKVGGNY | S | 440 | 449 | HLA class I | HTMA | (Snyder et al., 2020) |
| NLNESLIDL | S | 1192 | 1200 | HLA class I | HTMA | (Snyder et al., 2020) |
| NLTTRTQL | S | 17 | 24 | HLA class I | HTMA | (Snyder et al., 2020) |
| NQKLIANQF | S | 919 | 927 | B*15:01/B*52:01 | HTMA/multimer staining/AIM | (Snyder et al., 2020; Minervina et al., 2022; Tarke et al., 2022) |
| NSASFSTFK | S | 370 | 378 | A*68:01/A*11:01 | AIM/ICS | (Tarke et al., 2021; Jin et al., 2021) |
| NSFTRGVYY | S | 30 | 38 | A*68:01/A*29:02/A*26:01 | AIM | (Tarke et al., 2021) |
| NSIAIPTNF | S | 710 | 718 | B*57:01/B*52:01 | AIM | (Tarke et al., 2021; Tarke et al., 2022) |
| NTSNQVAVL | S | 603 | 611 | C*16:02 | AIM | (Tarke et al., 2022) |
| NTSNQVAVLY | S | 603 | 612 | A*26:01 | AIM | (Tarke et al., 2021) |
| NVYADSFVIR | S | 394 | 403 | A*68:01/A*33:03 | AIM/ICS | (Tarke et al., 2021; Jin et al., 2021) |
| NYNYLYRLF | S | 448 | 456 | A*24:02 | multimer staining /AIM/ELISPOT/ICS | (Zhang et al., 2021; Tarke et al., 2021; Wagner et al., 2022; Hu et al., 2022; Jin et al., 2021; Kared et al., 2021; Gangaev et al., 2021; Minervina et al., 2022; Rowntree et al., 2021) |
| NYNYLYRLFRK | S | 448 | 458 | HLA class I | HTMA | (Snyder et al., 2020) |
| NYNYRYRLF | S | 448 | 456 | A*24:02 | ICS | (Zhang et al., 2021) |
| PFFSNVTWF | S | 57 | 65 | A*24:02 | multimer staining | (Saini et al., 2021) |
| PWYIWLGFI | S | 1213 | 1221 | A*24:02 | ICS | (Shimizu et al., 2021) |
| PYRVVVLSF | S | 507 | 515 | A*24:02 | ICS | (Jin et al., 2021) |
| QELGKYEQY | S | 1201 | 1209 | B*44:02/B*44:03 | AIM | (Tarke et al., 2021) |
| QEVFAQVKQIY | S | 779 | 789 | B*44:02/B*44:03 | AIM | (Tarke et al., 2021) |
| QEVFAQVKQIYK | S | 779 | 790 | HLA class I | HTMA | (Snyder et al., 2020) |
| QIAPGQTGK | S | 409 | 417 | A*68:01 | AIM | (Tarke et al., 2021) |
| QIPFAMQMAY | S | 895 | 904 | B*35:01 | AIM | (Tarke et al., 2021) |
| QLNRALTGI | S | 762 | 770 | A*02:03 | proliferation | (Jin et al., 2021) |
| QLTPTWRVY | S | 628 | 636 | A*30:02/A*32:01/ A*02:01/B*07:02 | AIM/ multimer staining | (Tarke et al., 2021; Tarke et al., 2022) |
| QPTESIVRF | S | 321 | 329 | B*35:01/B*07:02 | AIM/ICS | (Tarke et al., 2021; Wagner et al., 2022) |
| QPTESIVRFPNITNL | S | 321 | 335 | HLA class I | AIM | (Zhao et al., 2021) |
| QPYRVVVL | S | 506 | 513 | B*08:01/B*07:02 | AIM | (Tarke et al., 2021) |
| QPYRVVVLSF | S | 506 | 515 | B*07:02 | AIM | (Tarke et al., 2021) |
| QPYRVVVLSFELLHA | S | 506 | 520 | HLA class I | ICS/AIM | (Mahajan et al., 2021) |
| QQLIRAAEIRASANL | S | 1010 | 1024 | HLA class I | ICS | (Titov et al., 2022) |
| QSAPHGVVF | S | 1054 | 1062 | C*07:02/C*03:04 | multimer staining/AIM | (Saini et al., 2021; Tarke et al., 2022) |
| QTNSPRRAR | S | 677 | 685 | A*31:01/A*33:03 | AIM/ICS | (Tarke et al., 2021; Jin et al., 2021) |
| QYIKWPWYI | S | 1208 | 1216 | A*23:01/A*24:02/C*06:02 | multimer staining /AIM/ICS/cytotoxicity/ELISA/ELISPOT | (Saini et al., 2021; Tarke et al., 2021; Wagner et al., 2022; Titov et al., 2022; Ferretti et al., 2020; Nelde et al., 2021; Kared et al., 2021; Gangaev et al., 2021; Minervina et al., 2022; Shimizu et al., 2021; Rowntree et al., 2021) |
| QYIKWPWYIW | S | 1208 | 1217 | A*23:01 | AIM | (Tarke et al., 2021) |
| QYIKWPWYIWLGFIA | S | 1208 | 1222 | A*24:02 | ICS | (Shimizu et al., 2021) |
| RFPNITNLCPF | S | 328 | 338 | A*24:02 | AIM | (Tarke et al., 2021) |
| RASANLAATK | S | 1019 | 1028 | A*03:01 | AIM | (Tarke et al., 2021) |
| RDIADTTDAV | S | 567 | 576 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| REGVFVSNGTHW | S | 1091 | 1102 | B*44:03 | AIM/HTMA | (Snyder et al., 2020; Tarke et al., 2021) |
| RFASVYAWNR | S | 346 | 355 | A*31:01 | AIM | (Tarke et al., 2021) |
| RFDNPVLPF | S | 78 | 86 | A*24:02/C*07:02 | AIM/HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020; Tarke et al., 2021; Kared et al., 2021) |
| RISNCVADY | S | 357 | 365 | HLA class I | HTMA | (Snyder et al., 2020) |
| RISNCVADYSVLYNS | S | 357 | 371 | HLA class I | ELISPOT | (Zhao et al., 2021) |
| RLDKVEAEV | S | 983 | 991 | A*02:01 | ELISPOT/HTMA/multimer staining /proliferation/ICS | (Saini et al., 2021; Snyder et al., 2020; Hu et al., 2022; Jin et al., 2021; Pan et al., 2021) |
| RLDKVEAEVQI | S | 983 | 993 | A*02:01 | multimer staining | (Saini et al., 2021) |
| RLFRKSNLK | S | 454 | 462 | A*31:01/A*03:01/A*11:01 | AIM/HTMA/ICS | (Snyder et al., 2020; Tarke et al., 2021; Wagner et al., 2022) |
| RLITGRLQSL | S | 995 | 1004 | A*02:01 | multimer staining | (Pan et al., 2021) |
| RLNEVAKNL | S | 1185 | 1193 | A*02:01 | multimer staining/HTMA | (Snyder et al., 2020; Gangaev et al., 2021; Qiu et al., 2021) |
| RLQSLQIYV | S | 1000 | 1008 | A*02:01 | AIM | (Wu et al., 2022) |
| RLQSLQTY | S | 1000 | 1007 | B*15:01 | AIM | (Tarke et al., 2021) |
| RLQSLQTYV | S | 1000 | 1008 | A*02:01/B*13:02/A*02:03 | multimer staining /AIM/ELISPOT/ ELISA/ICS/ x-ray crystallography/ SPR | (Tarke et al., 2021; Titov et al., 2022; Jin et al., 2021; Poran et al., 2020; Prakash et al., 2021; Wu et al., 2022) |
| RNFYEPQII | S | 1107 | 1115 | B*52:01 | AIM | (Tarke et al., 2022) |
| RSVASQSII | S | 685 | 693 | B*57:01 | AIM | (Tarke et al., 2021) |
| RSVASQSIIAYTMSL | S | 685 | 699 | HLA class I | HTMA | (Snyder et al., 2020) |
| RVDFCGKGY | S | 1039 | 1047 | HLA class I | HTMA | (Snyder et al., 2020) |
| RVQPTESIVRF | S | 319 | 329 | B*07:02 | multimer staining | (Saini et al., 2021) |
| RVVVLSFEL | S | 509 | 517 | A*32:01 | AIM | (Tarke et al., 2022) |
| RVVVLSFELLHAPAT | S | 509 | 523 | B*50:02 | ELISPOT | (Zhao et al., 2021) |
| RVYSTGSNV | S | 634 | 642 | A*30:01 | AIM | (Tarke et al., 2021) |
| RVYSTGSNVF | S | 634 | 643 | B*15:01/A*24:02 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| SANNCTFEY | S | 162 | 170 | A*29:02/B*35:01 | AIM | (Tarke et al., 2021) |
| SASFSTFKCY | S | 371 | 380 | A*01:01 | multimer staining | (Saini et al., 2021) |
| SASFSTFKCYGVSPT | S | 371 | 385 | HLA class I | ICS | (Zhang et al., 2022) |
| SEPVLKGVKL | S | 1261 | 1270 | B*40:01 | AIM/ELISA/HTMA | (Snyder et al., 2020; Tarke et al., 2021; Titov et al., 2022) |
| SETKCTLKSF | S | 297 | 306 | B*44:02/B*44:03 | AIM | (Tarke et al., 2021) |
| SETKCTLKSFTVEK | S | 297 | 310 | HLA class I | HTMA | (Snyder et al., 2020) |
| SFELLHAPATV | S | 514 | 524 | A*02:01 | multimer staining | (Saini et al., 2021) |
| SFIEDLLF | S | 816 | 823 | A*24:02 | multimer staining | (Saini et al., 2021) |
| SFKEELDKY | S | 1147 | 1155 | A*29:02 | AIM | (Tarke et al., 2021) |
| SFPQSAPHGVVF | S | 1051 | 1062 | A*24:02 | AIM | (Tarke et al., 2021) |
| SIIAYTMSL | S | 691 | 699 | B*08:01/A*02:01 | ICS/AIM/multimer staining/ELISPOT | (Tarke et al., 2021; Habel et al., 2020; Quiros-Fernandez et al., 2021; Agerer et al., 2021; Prakash et al., 2021) |
| SIIAYTMSLGAENSV | S | 691 | 705 | HLA class I | ELISPOT | (Mateus et al., 2020) |
| SKRVDFCGKGY | S | 1037 | 1047 | A*01:01 | multimer staining | (Saini et al., 2021) |
| SLIDLQEL | S | 1196 | 1203 | A*02:01 | multimer staining | (Saini et al., 2021) |
| SLIDLQELGK | S | 1196 | 1205 | A*11:01 | ICS | (Jin et al., 2021) |
| SNCVADYSVLYNSAS | S | 359 | 373 | HLA class I | ELISA | (Li et al., 2021) |
| SPRRARSV | S | 680 | 687 | B*08:01/B*07:02 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| SPRRARSVA | S | 680 | 688 | B*07:02 | ICS/multimer staining | (Saini et al., 2021; Schulien et al., 2021) |
| SRLDKVEAEV | S | 982 | 991 | A*02:01 | AIM | (Tarke et al., 2022) |
| SSANNCTFEY | S | 161 | 170 | A*01:01 | multimer staining | (Saini et al., 2021) |
| SSANNCTFEYVSQPF | S | 161 | 175 | HLA class I | ELISPOT | (Zhao et al., 2021) |
| STECSNLLLQY | S | 746 | 756 | A*01:01 | multimer staining | (Saini et al., 2021) |
| STGSNVFQTR | S | 637 | 646 | A*31:01/A*68:01 | AIM | (Tarke et al., 2021; Tarke et al., 2022) |
| STQDLFLPF | S | 50 | 58 | A*01:01/C*16:02 | ELISPOT/multimer staining/AIM | (Saini et al., 2021; Somogyi et al., 2021; Tarke et al., 2022) |
| STQDLFLPFF | S | 50 | 59 | A*01:01 | HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020) |
| SVASQSIIAY | S | 686 | 695 | A*26:01/A*29:02 | AIM | (Tarke et al., 2021) |
| SVASQSIIAYTMSLG | S | 686 | 700 | HLA class I | ELISPOT | (Mateus et al., 2020) |
| SVLNDILSR | S | 975 | 983 | A*68:01 | AIM | (Tarke et al., 2021) |
| SVLNDILSRL | S | 975 | 984 | HLA class I | HTMA | (Snyder et al., 2020) |
| SVYAWNRKR | S | 349 | 357 | A*03:01/A*33:03 | AIM/ICS | (Tarke et al., 2021; Jin et al., 2021) |
| SWMESEFRV | S | 151 | 159 | A*24:02 | multimer staining | (Saini et al., 2021) |
| SWMESEFRVY | S | 151 | 160 | A*29:02 | AIM | (Tarke et al., 2021) |
| SYQTQTNSPRRA | S | 673 | 684 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| TDEMIAQY | S | 866 | 873 | A*01:01 | multimer staining | (Saini et al., 2021) |
| TECSNLLLQY | S | 747 | 756 | B*44:02/B*44:03 | AIM | (Tarke et al., 2021) |
| TEILPVSMTK | S | 724 | 733 | HLA class I | HTMA | (Snyder et al., 2020) |
| TEKSNIIRGW | S | 95 | 104 | B*44:02/B*44:03 | AIM/HTMA | (Snyder et al., 2020; Tarke et al., 2021) |
| TESIVRFPNITNL | S | 323 | 335 | B*40:01 | AIM | (Tarke et al., 2021) |
| TESNKKFLPFQQF | S | 553 | 565 | B*44:02 | AIM | (Tarke et al., 2021) |
| TFEYVSQPFLM | S | 167 | 177 | A*24:02 | multimer staining | (Saini et al., 2021) |
| TIADYNYKL | S | 417 | 425 | A*02:01 | ICS | (Zhang et al., 2021) |
| TLADAGFIK | S | 827 | 835 | A*03:01 | AIM | (Tarke et al., 2021) |
| TLDSKTQSL | S | 109 | 117 | A*02:01/B*08:01//C*07:02 | AIM/HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020; Tarke et al., 2021; Sekine et al., 2020) |
| TPCSFGGVSV | S | 588 | 597 | B*07:02 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| TPINLVRDL | S | 208 | 216 | B*07:02 | AIM/HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020; Tarke et al., 2021) |
| TQDLFLPFF | S | 51 | 59 | A*24:02 | multimer staining | (Saini et al., 2021) |
| TQLNRALTGI | S | 761 | 770 | HLA class I | HTMA | (Snyder et al., 2020) |
| TQLNRALTGIAVEQD | S | 761 | 775 | HLA class I | ICS | (Zhang et al., 2022) |
| TQNVLYENQK | S | 912 | 921 | HLA class I | HTMA | (Snyder et al., 2020) |
| TRFASVYAW | S | 345 | 353 | C*07:02 | multimer staining | (Saini et al., 2021) |
| TRTQLPPAY | S | 20 | 28 | C*07:02 | multimer staining | (Saini et al., 2021) |
| TSNQVAVLY | S | 604 | 612 | B*57:01/B*35:01/A*26:01 | AIM/HTMA | (Snyder et al., 2020; Tarke et al., 2021) |
| TVYDPLQPELDSFK | S | 1136 | 1149 | A*03:01 | AIM/HTMA | (Snyder et al., 2020; Tarke et al., 2021) |
| TYVPAQEKNFT | S | 1066 | 1076 | A*24:02 | multimer staining | (Saini et al., 2021) |
| VAIHADQLTPTW | S | 622 | 633 | B*57:01 | AIM | (Tarke et al., 2021) |
| VASQSIIAY | S | 687 | 695 | B*35:01/A*29:02/B*15:01 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| VEAEVQIDRLITGR | S | 987 | 1000 | HLA class I | HTMA | (Snyder et al., 2020) |
| VFAQVKQIY | S | 781 | 789 | A*29:02/C*07:01 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| VFNATRFASVYAWNR | S | 341 | 355 | HLA class I | ICS/AIM | (Mahajan et al., 2021) |
| VFVSNGTHW | S | 1094 | 1102 | A*24:02 | multimer staining | (Saini et al., 2021) |
| VFVSNGTHWF | S | 1094 | 1103 | A*24:02 | AIM | (Tarke et al., 2021) |
| VGGNYNYLY | S | 445 | 453 | A*29:02 | AIM | (Tarke et al., 2021) |
| VGYLQPRTF | S | 267 | 275 | A*02:01/B*07:02/B*51:01 | multimer staining/AIM | (Weingarten-Gabbay et al., 2021; Tarke et al., 2022) |
| VGYLQPRTFL | S | 267 | 276 | A*24:02 | multimer staining | (Saini et al., 2021) |
| VGYQPYRVV | S | 503 | 511 | C*06:02 | multimer staining | (Saini et al., 2021) |
| VFKNIDGYF | S | 193 | 201 | A*24:02 | AIM/ELISPOT/ICS | (Tarke et al., 2021; Hu et al., 2022; Rowntree et al., 2021) |
| VLKGVKLHY | S | 1264 | 1272 | A*29:02 | AIM | (Tarke et al., 2021) |
| VLNDILARL | S | 973 | 981 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| VLNDILSRL | S | 976 | 984 | A*02:01/A*32:01 | ELISPOT/multimer staining/AIM/ICS | (Saini et al., 2021; Habel et al., 2020; Xiao et al., 2022; Prakash et al., 2021; Tarke et al., 2022) |
| VLPFNDGVYFA | S | 83 | 93 | A*02:01 | multimer staining | (Saini et al., 2021) |
| VLPFNDGVYFASTEK | S | 83 | 97 | HLA class I | HTMA | (Snyder et al., 2020) |
| VLPPLLTDEMIAQYT | S | 860 | 874 | HLA class I | HTMA | (Snyder et al., 2020) |
| VLTESNKKF | S | 551 | 559 | B*15:01 | multimer staining | (Saini et al., 2021) |
| VRFPNITNL | S | 327 | 335 | B*13:02 | ELISA | (Titov et al., 2022) |
| VTWFHAIHV | S | 62 | 70 | A*02:01 | multimer staining | (Xiao et al., 2022; Deng et al., 2021) |
| VTWFHAISG | S | 62 | 70 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| VTYVPAQEK | S | 1065 | 1073 | A*30:01/A*03:01/A*11:01 | AIM/ICS | (Tarke et al., 2021; Jin et al., 2021) |
| VVFLHVTYV | S | 1060 | 1068 | A*02:01/A*02:06/C*16:02 | multimer staining/AIM/ELISA/ICS | (Saini et al., 2021; Tarke et al., 2021; Wagner et al., 2022; Titov et al., 2022; Kared et al., 2021; Tarke et al., 2022; Qiu et al., 2021) |
| VVNQNAQAL | S | 951 | 959 | C*15:02 | AIM | (Tarke et al., 2022) |
| VYAWNRKRI | S | 350 | 358 | A*24:02 | ICS | (Jin et al., 2021) |
| VYDPLQPEL | S | 1137 | 1145 | A*24:02 | ELISPOT | (Hu et al., 2022) |
| VYDPLQPELDSF | S | 1137 | 1148 | A*24:02 | AIM | (Tarke et al., 2021) |
| VYSSANNCTF | S | 159 | 168 | A*24:02 | AIM | (Tarke et al., 2021) |
| VYSSANNCTFEY | S | 159 | 170 | HLA class I | HTMA | (Snyder et al., 2020) |
| VYSTGSNVFQTR | S | 635 | 646 | HLA class I | HTMA | (Snyder et al., 2020) |
| VYYPDKVF | S | 36 | 43 | A*24:02 | AIM | (Tarke et al., 2021) |
| VYYPDKVFR | S | 36 | 44 | A*33:03 | ICS | (Jin et al., 2021) |
| VYYPDKVFRSSVLH | S | 36 | 49 | HLA class I | HTMA | (Snyder et al., 2020) |
| WFVTQRNFY | S | 1102 | 1110 | A*29:02 | AIM | (Tarke et al., 2021) |
| WIFGTTLDSK | S | 104 | 113 | HLA class I | HTMA | (Snyder et al., 2020) |
| WLGFIAGLI | S | 1217 | 1225 | A*24:02 | ICS | (Shimizu et al., 2021) |
| WPWYIWLGF | S | 1212 | 1220 | A*24:02 | ICS | (Shimizu et al., 2021) |
| WPWYIWLGFIAGLIA | S | 1212 | 1226 | A*24:02 | ICS | (Shimizu et al., 2021) |
| WTAGAAAYY | S | 258 | 266 | A*26:01/B*35:01/A*29:02/A*01:01 | AIM/ICS | (Tarke et al., 2021; Wagner et al., 2022) |
| WTAGAAAYYVGY | S | 258 | 269 | HLA class I | HTMA | (Snyder et al., 2020) |
| WTFGAGAAL | S | 886 | 894 | A*26:01 | AIM | (Tarke et al., 2021) |
| WYIWLGFIA | S | 1214 | 1222 | A*24:02 | ICS | (Shimizu et al., 2021) |
| YAWNRKRI | S | 351 | 358 | B*51:01 | AIM | (Tarke et al., 2021) |
| YECDIPIGAGI | S | 660 | 670 | B*40:01 | AIM | (Tarke et al., 2021) |
| YENQKLIANQF | S | 917 | 927 | B*44:02 | AIM | (Tarke et al., 2021) |
| YEQYIKWPW | S | 1206 | 1214 | B*44:03/B*44:02/A*24:02 | ICS/AIM | (Tarke et al., 2021; Schulien et al., 2021; Shimizu et al., 2021) |
| YEQYIKWPWYI | S | 1206 | 1216 | A*24:02 | HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020) |
| YFPLQSYGF | S | 489 | 497 | A*29:01/A*24:02/A*29:02 | ICS/HTMA/multimer staining/AIM | (Saini et al., 2021; Snyder et al., 2020; Wagner et al., 2022; Swaminathan et al., 2022; Panikkar et al., 2022) |
| YFQPRTFLL | S | A*02:01 | multimer staining | (Agerer et al., 2021) | ||
| YGFQPTNGV | S | 495 | 503 | B*51:01/A*02:01 | AIM/multimer staining | (Tarke et al., 2021; Xiao et al., 2022) |
| YHLMSFPQSA | S | 1047 | 1056 | HLA class I | HTMA | (Snyder et al., 2020) |
| YIKWPWYIW | S | 1209 | 1217 | A*24:02 | ICS | (Shimizu et al., 2021) |
| YIWLGFIAG | S | 1215 | 1223 | A*24:02 | ICS | (Shimizu et al., 2021) |
| YIWLGFIAGL | S | 1215 | 1224 | A*02:01 | multimer staining | (Qiu et al., 2021) |
| YLQLRTFLL | S | 269 | 277 | A*02:01 | AIM | (Wu et al., 2022) |
| YLQPRIFLL | S | 269 | 277 | A*02:01 | SPR | (Chaurasia et al., 2021) |
| YYHKNNKSW | S | 144 | 152 | A*24:02 | AIM | (Tarke et al., 2021) |
| YLQPRTFLL | S | 269 | 277 | B*08:01/A*02:01/B*07:02/A*24:02 | SPR/ELISPOT/multimer staining /AIM /ICS/ELISA/ x-ray crystallography /cytotoxicity | (Saini et al., 2021; Tarke et al., 2021; Weingarten-Gabbay et al., 2021; Wagner et al., 2022; Habel et al., 2020; Titov et al., 2022; Swaminathan et al., 2022; Ferretti et al., 2020; Somogyi et al., 2021; Panikkar et al., 2022; Kared et al., 2021; Gangaev et al., 2021; Sekine et al., 2020; Quiros-Fernandez et al., 2021; Agerer et al., 2021; Minervina et al., 2022; Wu et al., 2022; Chaurasia et al., 2021) |
| YLYRLFRKSNLKPFE | S | 451 | 465 | HLA class I | AIM | (Mahajan et al., 2021) |
| YNYKLPDDFTGCVIA | S | 421 | 435 | HLA class I | ICS/AIM | (Mahajan et al., 2021) |
| YNYLYRLFR | S | 449 | 457 | A*31:01 | AIM | (Tarke et al., 2021) |
| YQAGSTPCNGVEGFN | S | 473 | 487 | A*02:06 | ELISPOT | (Zhao et al., 2021) |
| YQDVNCTEV | S | 612 | 620 | A*02:01/A*02:06 | multimer staining/AIM | (Tarke et al., 2021; Qiu et al., 2021) |
| YQPYRVVVL | S | 505 | 513 | C*06:02 | multimer staining | (Saini et al., 2021) |
| YSVLYNSASFSTFK | S | 365 | 378 | HLA class I | HTMA | (Snyder et al., 2020) |
| YTMSLGAENSVAY | S | 695 | 707 | A*26:01 | AIM | (Tarke et al., 2021) |
| YTNSFTRGVY | S | 28 | 37 | A*01:01/A*26:01/C*16:02 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021; Tarke et al., 2022) |
| YTNSFTRGVYY | S | 28 | 38 | A*01:01 | multimer staining | (Saini et al., 2021) |
| YVGYLQPRTFLLKYN | S | 266 | 280 | HLA class I | ICS/AIM | (Mahajan et al., 2021) |
| YYVGYLQPR | S | 265 | 273 | A*33:03 | ICS | (Jin et al., 2021) |
| YYVGYLQPRTF | S | 265 | 275 | A*24:02 | AIM | (Tarke et al., 2021) |
| YYVGYLQPRTFLL | S | 265 | 277 | A*02:01 | HTMA | (Snyder et al., 2020) |
| AAVYRINW | M | 68 | 75 | B*57:01 | AIM | (Tarke et al., 2021) |
| AGDSGFAAY | M | 188 | 196 | A*01:01 | AIM | (Tarke et al., 2021) |
| AIAMACLVGLM | M | 81 | 91 | HLA class I | HTMA | (Snyder et al., 2020) |
| AMACLVGLM | M | 83 | 91 | A*02:03 | ICS | (Jin et al., 2021) |
| ANRNRFLYI | M | 40 | 48 | B*08:01 | multimer staining | (Saini et al., 2021) |
| ASQRVAGDSGFAAY | M | 183 | 196 | HLA class I | HTMA | (Snyder et al., 2020) |
| ATSRTLSYY | M | 171 | 179 | A*11:01/B*57:01/A*01:01 | AIM/multimer staining /ELISA/cytotoxicity | (Tarke et al., 2021; Titov et al., 2022; Ferretti et al., 2020; Gangaev et al., 2021) |
| ATSRTLSYYK | M | 171 | 180 | A*30:01 | AIM/ELISA/multimer staining/ELISPOT/proliferation/cytotoxicity | (Tarke et al., 2021; Titov et al., 2022; Ferretti et al., 2020; Jin et al., 2021; Zhang et al., 2022) |
| ATSRTLSYYKLGASQ | M | 171 | 185 | HLA class I | ICS | (Heide et al., 2021) |
| AVILRGHLR | M | 142 | 150 | A*68:01 | AIM/HTMA | (Snyder et al., 2020; Tarke et al., 2021) |
| AYANRNRF | M | 38 | 45 | A*24:02 | multimer staining | (Saini et al., 2021) |
| AYANRNRFL | M | 38 | 46 | A*24:02 | multimer staining | (Saini et al., 2021) |
| CLVGLMWLSYFIASF | M | 86 | 100 | HLA class I | ICS | (Heide et al., 2021) |
| DSGFAAYSR | M | 190 | 198 | A*68:01 | AIM | (Tarke et al., 2021) |
| EELKKLLEQWNLVIG | M | 11 | 25 | HLA class I | ICS | (Heide et al., 2021) |
| ELVIGAVILR | M | 137 | 146 | A*68:01 | AIM | (Tarke et al., 2021) |
| FAYANRNRF | M | 37 | 45 | B*35:01/B*15:01 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| FIASFRLFA | M | 96 | 104 | A*02:03 | ICS | (Jin et al., 2021) |
| FIASFRLFARTRSMW | M | 96 | 110 | HLA class I | ICS | (Heide et al., 2021) |
| FLFLTWICL | M | 26 | 34 | A*02:01 | multimer staining/ICS | (Habel et al., 2020; Poran et al., 2020) |
| FLFLTWICLL | M | 26 | 35 | A*02:01 | ICS | (Jin et al., 2021) |
| FLWLLWPVTL | M | 53 | 62 | A*02:01 | multimer staining | (Saini et al., 2021; Pan et al., 2021) |
| FLYIIKLIFL | M | 45 | 54 | A*02:07 | ICS | (Jin et al., 2021) |
| FRLFARTRSM | M | 100 | 109 | B*08:01 | multimer staining | (Saini et al., 2021) |
| FVLAAVYRI | M | 65 | 73 | A*02:01/A*68:02 | Multime staining /cytotoxicity/ICS/AIM |
(Tarke et al., 2021; Deng et al., 2021; Pan et al., 2021) |
| GAVILRGHLRIAGHH | M | 141 | 155 | HLA class I | ICS | (Heide et al., 2021) |
| GFMWLSYFI | M | 89 | 97 | A*02:01 | multimer staining | (Agerer et al., 2021) |
| GLMWLSYFI | M | 89 | 97 | A*02:01 | multimer staining/ICS/ELISPOT | (Saini et al., 2021; Jin et al., 2021; Agerer et al., 2021; Prakash et al., 2021; Deng et al., 2021; Pan et al., 2021) |
| GTITVEELK | M | 6 | 14 | A*68:01 | AIM/HTMA | (Snyder et al., 2020; Tarke et al., 2021) |
| GTITVEELKKLLEQW | M | 6 | 20 | HLA class I | ICS | (Heide et al., 2021) |
| HLRIAGHHL | M | 148 | 156 | B*08:01/A*30:01 | ELISA/multimer staining/ICS | (Saini et al., 2021; Titov et al., 2022; Jin et al., 2021) |
| HLRIAGHHLGR | M | 148 | 158 | HLA class I | HTMA | (Snyder et al., 2020) |
| IAMACLVGL | M | 82 | 90 | A*02:06 | ICS/proliferation | (Jin et al., 2021) |
| IASFRLFAR | M | 97 | 105 | A*33:01 | AIM | (Tarke et al., 2021) |
| IFLWLLWPV | M | 52 | 60 | A*02:01 | ELISPOT | (Prakash et al., 2021) |
| IKDLPKEITVATSRT | M | 161 | 175 | HLA class I | ICS | (Heide et al., 2021) |
| ILRGHLRIA | M | 144 | 152 | A*02:03 | proliferation | (Jin et al., 2021) |
| KEITVATSRTLSYYK | M | 166 | 180 | HLA class I | ICS | (Heide et al., 2021) |
| KLLEQWNLV | M | 15 | 23 | A*02:01 | AIM/ICS | (Tarke et al., 2021; Habel et al., 2020; Jin et al., 2021) |
| LAAVYRINW | M | 67 | 75 | B*57:01 | AIM | (Tarke et al., 2021) |
| LAAVYRINWI | M | 67 | 76 | HLA class I | HTMA | (Snyder et al., 2020) |
| LLWPVTLAC | M | 56 | 64 | A*02:01 | multimer staining | (Saini et al., 2021) |
| LLWPVTLACFV | M | 56 | 66 | A*02:01 | multimer staining | (Pan et al., 2021) |
| LPKEITVAT | M | 164 | 172 | B*07:02 | AIM | (Tarke et al., 2021) |
| LQFAYANRNRFLY | M | 35 | 47 | HLA class I | HTMA | (Snyder et al., 2020) |
| LSYFIASFR | M | 93 | 101 | A*31:01/A*68:01/A*11:01 | AIM/proliferation | (Tarke et al., 2021; Jin et al., 2021) |
| LSYYKLGASQRVAGD | M | 176 | 190 | HLA class I | ICS | (Heide et al., 2021) |
| LVIGAVILR | M | 138 | 146 | A*68:01/A*11:01 | AIM/ICS | (Tarke et al., 2021; Jin et al., 2021) |
| LWLLWPVTL | M | 54 | 62 | A*24:02 | ICS | (Rowntree et al., 2021) |
| LWPVTLACF | M | 57 | 65 | A*24:02 | ICS | (Jin et al., 2021; Rowntree et al., 2021) |
| LYIIKLIFLW | M | 46 | 55 | A*24:02 | ICS | (Jin et al., 2021) |
| MACLVGLMW | M | 84 | 92 | B*57:01 | AIM | (Tarke et al., 2021) |
| NGTITVEELK | M | 5 | 14 | A*68:01 | AIM | (Tarke et al., 2021) |
| NRFLYIIKL | M | 43 | 51 | B*08:01/C*07:02 | ELISA/multimer staining/ELISPOT/ICS | (Saini et al., 2021; Titov et al., 2022; Nelde et al., 2021) |
| NRNRFLYIIKLIFLW | M | 41 | 55 | HLA class I | ICS | (Heide et al., 2021) |
| QFAYANRNRFLYIIK | M | 36 | 50 | HLA class I | ICS | (Heide et al., 2021) |
| QWNLVIGFLF | M | 19 | 28 | A*24:02 | ICS | (Jin et al., 2021) |
| RFLYIIKLIF | M | 44 | 53 | A*24:02 | multimer staining/ICS | (Saini et al., 2021; Jin et al., 2021) |
| RGHLRIAGHHLGRCD | M | 146 | 160 | HLA class I | ICS | (Heide et al., 2021) |
| RIAGHHLGR | M | 150 | 158 | A*03:01 | AIM | (Tarke et al., 2021) |
| RLFARTRS | M | 101 | 108 | HLA class I | ELISPOT | (Somogyi et al., 2021) |
| RLFARTRSM | M | 101 | 109 | A*30:01 | AIM | (Tarke et al., 2021) |
| RLFARTRSMW | M | 101 | 110 | HLA class I | HTMA | (Snyder et al., 2020) |
| RLFARTRSMWSFNPE | M | 101 | 115 | HLA class I | ICS | (Heide et al., 2021) |
| RNRFLYIIK | M | 42 | 50 | A*30:01 | AIM/proliferation/ICS | (Tarke et al., 2021; Jin et al., 2021) |
| RNRFLYIIKL | M | 42 | 51 | C*07:01 | multimer staining | (Saini et al., 2021) |
| RPLLESEL | M | 131 | 138 | B*07:02 | AIM | (Tarke et al., 2021) |
| RTRSMWSF | M | 105 | 112 | B*57:01 | AIM | (Tarke et al., 2021) |
| RTRSMWSFN | M | 105 | 113 | A*30:01 | proliferation/ICS | (Jin et al., 2021) |
| RVAGDSGFAAY | M | 186 | 196 | B*15:01/A*01:01 | AIM/multimer staining/ICS | (Saini et al., 2021; Tarke et al., 2021; Minervina et al., 2022) |
| RVAGDSGFAAYSRY | M | 186 | 199 | A*30:02 | AIM | (Tarke et al., 2021) |
| RVAGDSGFAAYSRYR | M | 186 | 200 | HLA class I | ICS | (Heide et al., 2021) |
| RYRIGNYKL | M | 198 | 206 | A*30:01/A*24:02 | AIM/ELISA/HTMA/ICS | (Saini et al., 2021; Snyder et al., 2020; Tarke et al., 2021; Titov et al., 2022; Jin et al., 2021; Rowntree et al., 2021) |
| SELVIGAVI | M | 136 | 144 | B*44:02 | AIM | (Tarke et al., 2021) |
| SELVIGAVIL | M | 136 | 145 | B*40:10/B*40:01 | HTMA/ELISPOT/ICS | (Snyder et al., 2020; Wagner et al., 2022; Nelde et al., 2021) |
| SELVIGAVILRGHLR | M | 136 | 150 | HLA class I | ICS | (Heide et al., 2021) |
| SFNPETNIL | M | 111 | 119 | B*08:01 | multimer staining | (Saini et al., 2021) |
| SFNPETNILLNVPLH | M | 111 | 125 | HLA class I | ICS | (Heide et al., 2021) |
| SFRLFARTR | M | 99 | 107 | A*33:03 | ICS | (Jin et al., 2021) |
| SGFAAYSRYRIGNYK | M | 191 | 205 | HLA class I | ICS | (Heide et al., 2021) |
| SMWSFNPET | M | 108 | 116 | A*02:01 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| SMWSFNPETNIL | M | 108 | 119 | HLA class I | HTMA | (Snyder et al., 2020) |
| SQRVAGDSGF | M | 184 | 193 | B*15:01 | multimer staining | (Saini et al., 2021) |
| SSSDNIALL | M | 212 | 220 | A*68:02 | AIM | (Tarke et al., 2021) |
| SYFIASFRL | M | 94 | 102 | A*24:02 | ICS | (Rowntree et al., 2021) |
| SYFIASFRLF | M | 94 | 103 | A*24:02 | ICS | (Jin et al., 2021) |
| SYFIASFRLFA | M | 94 | 104 | HLA class I | HTMA | (Snyder et al., 2020) |
| TLACFVLAAV | M | 61 | 70 | A*02:07/A*02:01 | multimer staining /ICS/proliferation | (Jin et al., 2021; Deng et al., 2021) |
| TRSMWSFNPETNILL | M | 106 | 120 | HLA class I | ICS | (Heide et al., 2021) |
| TSRTLSYYK | M | 172 | 180 | A*30:01 | ICS | (Jin et al., 2021) |
| TVATSRTLSY | M | 169 | 178 | A*01:01 | multimer staining | (Saini et al., 2021; Gangaev et al., 2021) |
| TVATSRTLSYYK | M | 169 | 180 | HLA class I | HTMA | (Snyder et al., 2020) |
| VATSRTLSY | M | 170 | 178 | B*35:01/B*07:02/A*01:01 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021; Weingarten-Gabbay et al., 2021) |
| VATSRTLSYY | M | 170 | 179 | A*01:01 | multimer staining | (Saini et al., 2021) |
| VPLHGTIL | M | 122 | 129 | B*07:02 | AIM | (Tarke et al., 2021) |
| VTLACFVLA | M | 60 | 68 | A*02:06 | proliferation | (Jin et al., 2021) |
| WICLLQFAY | M | 31 | 39 | HLA class I | HTMA | (Snyder et al., 2020) |
| WLLWPVTLA | M | 55 | 63 | A*02:01 | ICS | (Habel et al., 2020) |
| YANRNRFLY | M | 39 | 47 | B*35:01/A*01:01 | AIM/ELISA | (Tarke et al., 2021; Titov et al., 2022) |
| YSRYRIGNYK | M | 196 | 205 | A*30:01/A*11:01 | AIM/proliferation | (Tarke et al., 2021; Jin et al., 2021) |
| YSRYRIGNYKLNTDH | M | 196 | 210 | HLA class I | ICS | (Heide et al., 2021) |
| YYKLGASQR | M | 178 | 186 | A*33:03 | ICS | (Jin et al., 2021) |
| AAGLEAPFLY | ORF3a | 98 | 107 | A*01:01 | multimer staining | (Saini et al., 2021) |
| AAGLEAPFLYLY | ORF3a | 98 | 109 | B*44:02 | AIM | (Tarke et al., 2021) |
| AGLEAPFLY | ORF3a | 99 | 107 | A*29:02 | AIM | (Tarke et al., 2021) |
| ALLAVFQSA | ORF3a | 51 | 59 | A*02:01 | multimer staining | (Saini et al., 2021) |
| ALSKGVHFV | ORF3a | 72 | 80 | A*02:01 | ELISA/HTMA/multimer staining/ELISPOT | (Saini et al., 2021; Snyder et al., 2020; Titov et al., 2022; Nelde et al., 2021; Kared et al., 2021; Minervina et al., 2022) |
| APFLYLYAL | ORF3a | 103 | 111 | B*08:01/B*07:02 | multimer staining | (Saini et al., 2021) |
| ATIPIQASL | ORF3a | 33 | 41 | B*57:01 | AIM | (Tarke et al., 2021) |
| CRSKNPLLY | ORF3a | 133 | 141 | C*06:02 | multimer staining | (Saini et al., 2021) |
| DYYQLYSTQL | ORF3a | 210 | 219 | A*24:02 | multimer staining | (Saini et al., 2021) |
| EEHVQIHTI | ORF3a | 241 | 249 | HLA class I | HTMA | (Snyder et al., 2020) |
| FLYLYALVY | ORF3a | 105 | 113 | C*07:02 | multimer staining | (Saini et al., 2021) |
| FTIGTVTLK | ORF3a | 8 | 16 | A*68:01 | AIM | (Tarke et al., 2021) |
| FTSDYYQLY | ORF3a | 207 | 215 | A*01:01/A*24:02 | ICS/multimer staining/AIM/ELISA/cytotoxicity | (Saini et al., 2021; Tarke et al., 2021; Wagner et al., 2022; Titov et al., 2022; Schulien et al., 2021; Swaminathan et al., 2022; Ferretti et al., 2020; Panikkar et al., 2022; Kared et al., 2021; Gangaev et al., 2021; Peng et al., 2020; Minervina et al., 2022) |
| FVRATATIPI | ORF3a | 28 | 37 | HLA class I | HTMA | (Snyder et al., 2020) |
| FVRIIMRLW | ORF3a | 120 | 128 | B*57:01 | AIM | (Tarke et al., 2021) |
| FVTVYSHLL | ORF3a | 87 | 95 | A*02:01 | multimer staining | (Saini et al., 2021) |
| GLEAPFLYL | ORF3a | 100 | 108 | A*02:01 | AIM | (Tarke et al., 2021) |
| HSYFTSDYY | ORF3a | 204 | 212 | A*29:02 | AIM | (Tarke et al., 2021) |
| HVTFFIYNK | ORF3a | 227 | 235 | A*68:01 | AIM | (Tarke et al., 2021) |
| IPIQASLPF | ORF3a | 35 | 43 | B*35:01/B*51:01 | AIM/HTMA | (Snyder et al., 2020; Tarke et al., 2021) |
| IPYNSVTSSI | ORF3a | 158 | 167 | HLA class I | HTMA | (Snyder et al., 2020) |
| IPYNSVTSSIVI | ORF3a | 158 | 169 | B*51:01 | AIM | (Tarke et al., 2021) |
| ITLKKRWQL | ORF3a | 63 | 71 | B*08:01/B*57:01 | AIM | (Tarke et al., 2021) |
| ITLKKRWQLAL | ORF3a | 63 | 73 | HLA class I | HTMA | (Snyder et al., 2020) |
| IVGVALLAVF | ORF3a | 47 | 56 | HLA class I | HTMA | (Snyder et al., 2020) |
| IYDEPTTTT | ORF3a | 263 | 271 | C*07:02 | multimer staining | (Saini et al., 2021) |
| LEAPFLYLY | ORF3a | 101 | 109 | A*29:02 | AIM | (Tarke et al., 2021) |
| LLYDANYFL | ORF3a | 139 | 147 | A*02:01 | ICS/multimer staining/AIM/ELISA/cytotoxicity | (Saini et al., 2021; Weingarten-Gabbay et al., 2021; Wagner et al., 2022; Titov et al., 2022; Schulien et al., 2021; Swaminathan et al., 2022; Ferretti et al., 2020; Kared et al., 2021; Quiros-Fernandez et al., 2021; Minervina et al., 2022) |
| LPFGWLIV | ORF3a | 41 | 48 | B*51:01 | AIM | (Tarke et al., 2021) |
| LYLYALVYF | ORF3a | 106 | 114 | A*24:02 | AIM | (Tarke et al., 2021) |
| MDLFMRIFTI | ORF3a | 1 | 10 | HLA class I | HTMA | (Snyder et al., 2020) |
| NLLLLFVTV | ORF3a | 82 | 90 | A*02:01 | multimer staining/ICS | (Saini et al., 2021) |
| NPLLYDANY | ORF3a | 137 | 145 | B*53:01 | AIM | (Tarke et al., 2021) |
| NPLLYDANYFL | ORF3a | 137 | 147 | A*02:01 | multimer staining | (Saini et al., 2021) |
| NPLLYDANYFLCW | ORF3a | 137 | 149 | HLA class I | HTMA | (Snyder et al., 2020) |
| QSASKIITL | ORF3a | 57 | 65 | B*08:01 | AIM/multimer staining | (Saini et al., 2021; Tarke et al., 2021) |
| RIFTIGTVTLK | ORF3a | 6 | 16 | HLA class I | HTMA | (Snyder et al., 2020) |
| SASKIITLK | ORF3a | 58 | 66 | A*03:01/A*11:01 | multimer staining | (Kared et al., 2021) |
| SASKIITLKKRW | ORF3a | 58 | 69 | B*57:01 | AIM | (Tarke et al., 2021) |
| SEHDYQIGGYTEKW | ORF3a | 180 | 193 | HLA class I | HTMA | (Snyder et al., 2020) |
| SYFTSDYYQLY | ORF3a | 205 | 215 | A*24:02 | multimer staining | (Saini et al., 2021) |
| TLKKRWQLA | ORF3a | 64 | 72 | B*08:01 | multimer staining | (Saini et al., 2021) |
| TTSPISEHDY | ORF3a | 175 | 184 | HLA class I | HTMA | (Snyder et al., 2020) |
| TVYSHLLLV | ORF3a | 89 | 97 | A*02:01 | AIM | (Tarke et al., 2021) |
| VAAGLEAPF | ORF3a | 97 | 105 | B*35:01 | AIM | (Tarke et al., 2021) |
| VLHSYFTSDYYQLY | ORF3a | 202 | 215 | HLA class I | HTMA | (Snyder et al., 2020) |
| VYFLQSINF | ORF3a | 112 | 120 | A*24:02 | ICS/multimer staining/ELISPOT/ELISA/cytotoxicity | (Wagner et al., 2022; Ferretti et al., 2020; Nelde et al., 2021; Kared et al., 2021; Minervina et al., 2022) |
| VRIIMRLWL | ORF3a | 121 | 129 | C*07:02 | multimer staining | (Saini et al., 2021) |
| YFTSDYYQL | ORF3a | 206 | 214 | C*07:02 | multimer staining | (Saini et al., 2021) |
| YFTSDYYQLY | ORF3a | 206 | 215 | A*29:02/A*29:01/A*01:01 | AIM/ICS/multimer staining | (Saini et al., 2021; Tarke et al., 2021; Swaminathan et al., 2022; Panikkar et al., 2022) |
| YLYALVYFL | ORF3a | 107 | 115 | A*02:01 | ICS/multimer staining | (Schulien et al., 2021; Kared et al., 2021) |
| YYQLYSTQL | ORF3a | 211 | 219 | A*24:02/C*07:02 | /ELISPOTAIM/ELISA/HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020; Tarke et al., 2021; Titov et al., 2022; Nelde et al., 2021) |
| HLVDFQVTI | ORF6 | 3 | 11 | A*02:01 | ELISPOT/ELISA/HTMA/multimer staining | (Saini et al., 2021; Snyder et al., 2020; Titov et al., 2022; Prakash et al., 2021) |
| HLVDFQVTIA | ORF6 | 3 | 12 | A*02:01 | multimer staining | (Saini et al., 2021) |
| IIKNLSKSLTENKY | ORF6 | 36 | 49 | HLA class I | HTMA | (Snyder et al., 2020) |
| LDYIINLII | ORF6 | 29 | 37 | HLA class I | HTMA | (Snyder et al., 2020) |
| LIIMRTFKV | ORF6 | 16 | 24 | B*08:01 | multimer staining | (Saini et al., 2021) |
| RTFKVSIWNLDY | ORF6 | 20 | 31 | A*01:01 | ELISPOT | (Nelde et al., 2021) |
| SIWNLDYIINL | ORF6 | 25 | 35 | A*02:01 | multimer staining | (Saini et al., 2021) |
| TFKVSIWNL | ORF6 | 21 | 29 | B*08:01 | multimer staining | (Saini et al., 2021) |
| VTIAEILLI | ORF6 | 9 | 17 | HLA class I | HTMA | (Snyder et al., 2020) |
| EGNSPFHPL | ORF7a | 41 | 49 | B*08:01 | multimer staining | (Saini et al., 2021) |
| FACPDGVKHVY | ORF7a | 65 | 75 | A*01:01 | multimer staining | (Saini et al., 2021) |
| FAFACPDGVKHVYQL | ORF7a | 63 | 77 | HLA class I | HTMA | (Snyder et al., 2020) |
| FIRQEEVQELY | ORF7a | 87 | 97 | A*01:01/B*15:01 | multimer staining | (Saini et al., 2021) |
| GLITLSYHL | ORF7a | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) | ||
| HPLADNKFAL | ORF7a | 47 | 56 | B*08:01 | multimer staining | (Saini et al., 2021) |
| IRQEEVQEL | ORF7a | 88 | 96 | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| KFALTCFSTQF | ORF7a | 53 | 63 | A*24:02 | multimer staining | (Saini et al., 2021) |
| KLFIRQEEV | ORF7a | 85 | 93 | HLA class I | HTMA | (Snyder et al., 2020) |
| LLKEPCSSGTY | ORF7a | 30 | 40 | B*15:01 | multimer staining | (Saini et al., 2021) |
| QECVRGTTVL | ORF7a | 21 | 30 | HLA class I | HTMA | (Snyder et al., 2020) |
| QLRARSVSPK | ORF7a | 76 | 85 | A*03:01 | ELISA/ELISPOT | (Titov et al., 2022; Nelde et al., 2021) |
| RARSVSPKL | ORF7a | 78 | 86 | B*07:02 | multimer staining | (Kared et al., 2021) |
| RARSVSPKLFIR | ORF7a | 78 | 89 | HLA class I | HTMA | (Snyder et al., 2020) |
| SPFHPLADNKFAL | ORF7a | 44 | 56 | HLA class I | HTMA | (Snyder et al., 2020) |
| SPIFLIVAA | ORF7a | 98 | 106 | B*07:02 | multimer staining | (Saini et al., 2021) |
| VFITLCFTLK | ORF7a | 108 | 117 | HLA class I | HTMA | (Snyder et al., 2020) |
| VQELYSPIFLIV | ORF7a | 93 | 104 | HLA class I | HTMA | (Snyder et al., 2020) |
| YEGNSPFHPL | ORF7a | 40 | 49 | B*40:01 | HTMA/ELISPOT | (Snyder et al., 2020; Nelde et al., 2021) |
| IIFWFSLEL | ORF7b | 26 | 34 | A*02:01 | ELISPOT | (Prakash et al., 2021) |
| IMLIIFWFSL | ORF7b | 23 | 32 | HLA class I | HTMA | (Snyder et al., 2020) |
| EPKLGSLVV | ORF8 | 92 | 100 | B*07:02 | multimer staining | (Saini et al., 2021) |
| EYHDVRVVL | ORF8 | 110 | 118 | A*24:02 | multimer staining | (Saini et al., 2021) |
| EYHDVRVVLDF | ORF8 | 110 | 120 | A*24:02 | multimer staining | (Saini et al., 2021) |
| FLGIITTV | ORF8 | 6 | 13 | A*02:01 | multimer staining | (Saini et al., 2021) |
| GARKSAPLI | ORF8 | 50 | 58 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| GNYTVSCLPFTI | ORF8 | 77 | 88 | HLA class I | HTMA | (Snyder et al., 2020) |
| IQYIDIGNY | ORF8 | 71 | 79 | HLA class I | HTMA | (Snyder et al., 2020) |
| KLGSLVVRC | ORF8 | 94 | 102 | A*02:01 | multimer staining | (Saini et al., 2021) |
| LEYHDVRVVL | ORF8 | 109 | 118 | B*40:01 | ELISPOT | (Nelde et al., 2021) |
| QECSLQSCT | ORF8 | 18 | 26 | A*02:01 | multimer staining | (Xiao et al., 2022) |
| QSCTQHQPY | ORF8 | 23 | 31 | A*01:01 | multimer staining | (Saini et al., 2021) |
| RVGARKSAPL | ORF8 | 48 | 57 | HLA class I | HTMA | (Snyder et al., 2020) |
| VDDPCPIHFY | ORF8 | 33 | 42 | A*01:01 | multimer staining | (Saini et al., 2021) |
| YEDFLEYHDVRVVL | ORF8 | 105 | 118 | HLA class I | HTMA | (Snyder et al., 2020) |
| YIDIGNYTV | ORF8 | 73 | 81 | A*02:01 | ELISPOT/multimer staining | (Xiao et al., 2022; Prakash et al., 2021) |
| YVVDDPCPI | ORF8 | 31 | 39 | A*02:01 | ELISPOT | (Prakash et al., 2021) |
| YVVDDPCPIHFY | ORF8 | 31 | 42 | HLA class I | HTMA | (Snyder et al., 2020) |
| DEFVVVTV | ORF9b | 89 | 96 | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| ELPDEFVVV | ORF9b | 86 | 94 | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| ELPDEFVVVTV | ORF9b | 86 | 96 | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| KAFQLTPIAV | ORF9b | 67 | 76 | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| LEDKAFQL | ORF9b | 64 | 71 | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| SLEDKAFQL | ORF9b | 63 | 71 | A*02:01/B*07:02 | multimer staining | (Weingarten-Gabbay et al., 2021) |
| NVFAFPFTI | ORF10 | 5 | 13 | A*02:01/B*13:01 | ELISPOT | (Prakash et al., 2021; Ma et al., 2021) |
| NYIAQVDVVNFNL | ORF10 | 25 | 37 | HLA class I | HTMA | (Snyder et al., 2020) |
| SLLLCRMNSRNYIA | ORF10 | 15 | 28 | HLA class I | HTMA | (Snyder et al., 2020) |
| YINVFAFPF | ORF10 | 3 | 11 | A*02:01 | ELISPOT | (Prakash et al., 2021) |
Table 2.
List of CD4+ T-cell epitopes validated from SARS-CoV-2 antigens.
| Sequence | Protein | Start | End | HLA restriction | Methods to validate the epitope peptides | References |
|---|---|---|---|---|---|---|
| AADLDDFSKQLQQSM | N | 397 | 411 | DR | ELISPOT/ICS | (Nelde et al., 2021) |
| AAEASKKPRQKRTAT | N | 251 | 265 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| AALALLLLDRLNQLE | N | 217 | 231 | DRB1*11:01 | ELISA/CBA/AIM | (Panikkar et al., 2022; Verhagen et al., 2021) |
| AALALLLLDRLNQLESKMS | N | 217 | 235 | HLA class II | ELISA | (Verhagen et al., 2021) |
| AALALLLLDRLNQLESKMSG | N | 217 | 236 | DRB1*03:01/DRB1*11:01/DRB1*11:04/DRB3*01:01 | multimer staining | (Johansson et al., 2021) |
| ADETQALPQRQKKQQ | N | 376 | 390 | HLA class II | ICS | (Heide et al., 2021) |
| AFFGMSRIGMEVTPS | N | 313 | 327 | HLA class II | ELISPOT | (Keller et al., 2020) |
| AFFGMSRIGMEVTPSGTWLT | N | 313 | 332 | DRB1*04:01/DRB1*04:04/DRB1*11:01 | multimer staining /multimer staining | (Johansson et al., 2021) |
| AGNGGDAALALLLLD | N | 211 | 225 | DQB1*03:01/DQB1*06:02 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| AIKLDDKDPNFKDQV | N | 336 | 350 | DRB1*03:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| AIVLQLPQGTTLPKG | N | 156 | 170 | DR | ELISPOT | (Nelde et al., 2021) |
| ALALLLLDRLNQLESKM | N | 218 | 234 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| ALPQRQKKQQTVTLL | N | 381 | 395 | HLA class II | ICS | (Heide et al., 2021) |
| ANKDGIIWVATEGALNTPK | N | 125 | 143 | HLA class II | ELISA | (Verhagen et al., 2021) |
| AQFAPSASAFFGMSRIGMEV | N | 305 | 324 | DRB1*07:01/DRB1*11:01 | multimer staining | (Johansson et al., 2021) |
| ASAFFGMSRIGMEVT | N | 311 | 325 | DRB1*11:01/DRB1*11:04/DRB1*01:02/DRB1*14:01/DQB1*05:03/ | ICS/AIM/ELISPOT/ELISA | (Tarke et al., 2021; Titov et al., 2022; Nelde et al., 2021; Heide et al., 2021; Rammensee et al., 2021) |
| ASWFTALTQHGKEDL | N | 50 | 64 | DRB4*01:03 | ELISA/ICS/ELISPOT | (Titov et al., 2022; Nelde et al., 2021) |
| DAALALLLLDRLNQL | N | 216 | 230 | DPB1*02:01/DPA1*01:03/DPB1*04:01/DQA1*05:01/DQB1*02:01/DQA1*05:01/DQB1*03:01/DQA1*03:01/DQB1*03:02/DQA1*01:01/DQB1*05:01/DQA1*01:02/DQB1*06:02/DRB1*01:01/DRB1*04:01/DRB1*04:05/DRB1*08:02/DRB1*09:01/DRB1*11:01/DRB1*13:02/DRB3*01:01/DRB4*01:01/DRB5*01:01/DQB1*05:03/DRB1*15:01/DRB1*14:01/DRB1*12:01/DRB1*03:01/DQB1*06:02 | ICS/AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020; Heide et al., 2021) |
| DDFSKQLQQSMSSADSTQA | N | 401 | 419 | DRB1*11:01 | multimer staining | (Johansson et al., 2021) |
| DDQIGYYRRATRRIR | N | 81 | 95 | DPB1*02:01/DQA1*05:01/DQB1*03:01/DRB1*01:01/DRB1*04:01/DRB1*04:05/DRB1*07:01/DRB1*08:02/DRB1*09:01/DRB1*11:01/DRB3*01:01/DRB3*02:02/DRB5*01:01/DRB1*11:01/DRB1*01:01/DRB1*13:01/DRB1*16:02/DRB1*15:01/DRB1*14:06/DRB1*14:01 | ICS/AIM/ELISA/ELISPOT | (Tarke et al., 2021; Le Bert et al., 2020; Mateus et al., 2020; Heide et al., 2021; Verhagen et al., 2021) |
| DDQIGYYRRATRRIRGG | N | 81 | 97 | DRB1*11:01 | AIM | (Pogorelyy et al., 2022) |
| DDQIGYYRRATRRIRGGDG | N | 81 | 99 | HLA class II | ELISA | (Verhagen et al., 2021) |
| DDQIGYYRRATRRIRGGDGK | N | 81 | 100 | DRB1*11:01/DRB5*01:01 | multimer staining | (Johansson et al., 2021) |
| DKKKKADETQALPQR | N | 371 | 385 | HLA class II | ICS | (Heide et al., 2021) |
| DLSPRWYFYYLGTGP | N | 103 | 117 | HLA class II | ICS | (Schmidt et al., 2021) |
| DQIGYYRRATRRIRGG | N | 82 | 97 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| DYKHWPQIAQFAPSA | N | 297 | 311 | HLA class II | ELISA | (Verhagen et al., 2021) |
| DYKHWPQIAQFAPSASAFFG | N | 297 | 316 | DRB1*07:01 | multimer staining | (Johansson et al., 2021) |
| EGALNTPKDHIGTRN | N | 136 | 150 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| ERSGARSKQRRPQGL | N | 31 | 45 | HLA class II | ICS | (Heide et al., 2021) |
| ESKMSGKGQQQQGQT | N | 231 | 245 | HLA class II | ICS | (Heide et al., 2021) |
| FGDQELIRQGTDYKH | N | 286 | 300 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| FKDQVILLNKHIDAY | N | 346 | 360 | DPB1*02:01/DPA1*01:03/DPB1*04:01/DQA1*05:01/DQB1*02:01/DQA1*05:01/DQB1*03:01/DQA1*03:01/DQB1*03:02/DQA1*01:01/DQB1*05:01/DQA1*01:02/DQB1*06:02/DRB1*01:01/DRB1*04:01/DRB1*04:05/DRB1*07:01/DRB1*08:02/DRB1*09:01/DRB1*11:01/DRB1*12:01/DRB1*13:02/DRB3*01:01/DRB3*02:02/DRB4*01:01/DRB5*01:01/DQB1*06:02/DRB1*03:01/DRB1*16:02/DRB1*15:01/DRB1*14:06/DRB1*14:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| FPRGQGVPINTNSSP | N | 66 | 80 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| FYAEGSRGGSQASSR | N | 171 | 185 | HLA class II | ICS | (Heide et al., 2021) |
| GGDGKMKDLSPRWYF | N | 96 | 110 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| GIIWVATEGALNTPK | N | 129 | 143 | DRB1*04:01/DRB1*04:04 | AIM | (Panikkar et al., 2022) |
| GIIWVATEGALNTPKDHIGT | N | 129 | 148 | DRB1*04:01DRB1*04:04/DRB1*07:01 | multimer staining | (Johansson et al., 2021) |
| GKGQQQQGQTVTKKS | N | 236 | 250 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| GMEVTPSGTWLTYTG | N | 321 | 335 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| GMEVTPSGTWLTYTGAIKLD | N | 321 | 340 | DRB1*07:01/DRB5*01:01 | multimer staining/ICS | (Le Bert et al., 2020; Johansson et al., 2021) |
| GMSRIGMEVTPSGTW | N | 316 | 330 | HLA class II | ICS | (Heide et al., 2021) |
| GPEAGLPYGANKDGI | N | 116 | 130 | HLA class II | ICS | (Heide et al., 2021) |
| GTWLTYTGAIKLDDK | N | 328 | 342 | DR | ELISPOT/ICS/AIM | (Nelde et al., 2021) |
| GVPINTNSSPDDQIG | N | 71 | 85 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| GYYRRATRRIRGGDG | N | 85 | 99 | DRB1*08:01/DRB1*11:01 | AIM | (Panikkar et al., 2022) |
| HIDAYKTFPPTEPKK | N | 356 | 370 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| IGYYRRATRRIRGGD | N | 84 | 98 | DR11/DRB1*13:01/DRB1*11:01/DRB1*11:04 | ICS/ELISA/ELISPOT/AIM | (Titov et al., 2022; Nelde et al., 2021; Rammensee et al., 2021) |
| IKLDDKDPNFKDQVI | N | 337 | 351 | HLA class II | AIM | (Zhao et al., 2021) |
| ILLNKHIDAYKTFPP | N | 351 | 365 | DRB1*14:06/DRB1*15:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| IWVATEGALNTPKDH | N | 131 | 145 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| KAYNVTQAFGRRGPE | N | 266 | 280 | DPB1*02:01/DPA1*01:03/DPB1*04:01/DQA1*05:01/DQB1*03:01/DQA1*03:01/DQB1*03:02/DQA1*01:02/DQB1*06:02/DRB1*01:01/DRB1*04:01/DRB1*04:05/DRB1*07:01/DRB1*08:02/DRB1*09:01/DRB1*11:01/DRB1*13:02/DRB1*15:01/DRB3*01:01/DRB3*02:02/DRB4*01:01/DRB5*01:01 | ICS/AIM | (Tarke et al., 2021; Le Bert et al., 2020; Heide et al., 2021) |
| KDGIIWVATEGALNT | N | 127 | 141 | DR | ELISPOT/ICS/AIM | (Nelde et al., 2021) |
| KEDLKFPRGQGVPIN | N | 61 | 75 | HLA class II | ICS | (Heide et al., 2021) |
| KGFYAEGSRGGSQASSRSSS | N | 169 | 188 | DRB1*04:01 | multimer staining | (Johansson et al., 2021) |
| KKPRQKRTATKAYNV | N | 256 | 270 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021; Le Bert et al., 2021) |
| KPRQKRTATKAYNVT | N | 257 | 271 | DPA1*02:01/DPB1*14:01 | ELISPOT | (Keller et al., 2020) |
| KPRQKRTATKAYNVTQAFGR | N | 257 | 276 | DRB1*07:01/DRB5*01:01 | multimer staining | (Johansson et al., 2021) |
| KQQTVTLLPAADLDDF | N | 388 | 403 | DRB1 | ELISPOT | (Prakash et al., 2021) |
| KRTATKAYNVTQAFG | N | 261 | 275 | DQB1*06:02/DQB1*06:03 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| KTFPPTEPKKDKKKK | N | 361 | 375 | HLA class II | ICS | (Heide et al., 2021) |
| LIRQGTDYKHWPQIA | N | 291 | 305 | HLA class II | ICS/AIM | (Tarke et al., 2021; Le Bert et al., 2020; Heide et al., 2021) |
| LLLLDRLNQLESKMS | N | 221 | 235 | DPB1*02:01/DRB1*03:01/DRB1*04:01/DRB1*04:05/DRB1*07:01/DRB1*08:02/DRB1*09:01/DRB1*11:01/DRB1*12:01/DRB1*13:02/DRB1*15:01/DPA1*01:03/DPB1*04:01/DQA1*05:01/DQB1*02:01/DQA1*03:01/DQB1*03:02/DQA1*01:01/DQB1*05:01/DQA1*01:02/DQB1*06:02/DRB1*01:01/DRB3*01:01/DRB4*01:01/DRB5*01:01/DRB1*01:01/DRB1*11:01/DRB1*03:01/DRB1*15:01/DRB1*14:01/DRB1*12:01 | ICS/AIM/ELISPOT | (Tarke et al., 2021; Nelde et al., 2021; Mateus et al., 2020; Heide et al., 2021; Rammensee et al., 2021) |
| LNKHIDAYKTFPPTEPKKDK | N | 353 | 372 | DRB1*11:01/DPB1*04:01 | multimer staining | (Johansson et al., 2021) |
| LPNNTASWFTALTQHGKED | N | 45 | 63 | HLA class II | ELISA | (Verhagen et al., 2021) |
| LPQGTTLPKGFYAEG | N | 161 | 175 | HLA class II | ICS | (Heide et al., 2021) |
| LPQGTTLPKGFYAEGSRGGS | N | 161 | 180 | DRB1*04:01 | multimer staining | (Johansson et al., 2021) |
| LPYGANKDGIIWVAT | N | 121 | 135 | DPB1*02:01/DPA1*01:03/DPB1*04:01/DQA1*05:01/DQB1*02:01/DQA1*05:01/DQB1*03:01/DQA1*03:01/DQB1*03:02/DQA1*01:02/DQB1*06:02/DRB1*01:01/DRB1*03:01/DRB1*04:01/DRB1*04:05/DRB1*07:01/DRB1*08:02/DRB1*09:01/DRB1*11:01/DRB1*12:01/DRB1*15:01/DRB3*01:01/DRB3*02:02/DRB4*01:01/DRB5*01:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| LPYGANKDGIIWVATEGALN | N | 121 | 140 | DRB1*04:01/DRB1*04:04/DRB1*07:01 | multimer staining | (Johansson et al., 2021) |
| LTQHGKEDLKFPRGQ | N | 56 | 70 | HLA class II | AIM | (Tarke et al., 2021) |
| LTYTGAIKLDDKDPN | N | 331 | 345 | DRB1*07:01 | ICS,AIM | (Tarke et al., 2021; Heide et al., 2021) |
| MKDLSPRWYFYYLGT | N | 101 | 115 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| MKDLSPRWYFYYLGTGPEAG | N | 25 | 44 | HLA class II | ICS | (Le Bert et al., 2020) |
| MSDNGPQNQRNAPRI | N | 1 | 15 | HLA class II | ICS | (Heide et al., 2021) |
| NAPRITFGGPSDSTG | N | 11 | 25 | DQB1*03:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| NFGDQELIRQGTDYKHWPQ | N | 285 | 303 | HLA class II | ELISA/CBA | (Verhagen et al., 2021) |
| NFKDQVILLNKHIDAYKTF | N | 345 | 363 | HLA class II | ELISA | (Verhagen et al., 2021) |
| NFKDQVILLNKHIDAYKTFP | N | 345 | 364 | DRB1*11:01/DRB1*11:04/DPB1*04:01 | multimer staining | (Johansson et al., 2021) |
| NKDGIIWVATEGALN | N | 126 | 140 | DPB1*02:01/DPA1*01:03/DPB1*04:01/DQA1*05:01/DQB1*02:01/DQA1*05:01/DQB1*03:01/DQA1*03:01/DQB1*03:02/DQA1*01:02/DQB1*06:02/DRB1*01:01/DRB1*03:01/DRB1*04:01/DRB1*04:05/DRB1*08:02/DRB1*09:01/DRB1*11:01/DRB1*15:01/DRB3*01:01/DRB3*02:02/DRB4*01:01/DRB5*01:01/DQB1*02:01/DRB1*07:01/DRB1*04:04/DQB1*05:03/DQB1*03:02/DQB1*02:02 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| NSTPGSSKRTSPARM | N | 196 | 210 | HLA class II | ICS | (Heide et al., 2021) |
| PANNAAIVLQLPQGT | N | 151 | 165 | HLA class II | ICS | (Heide et al., 2021) |
| PNFKDQVILLNKHIDAYK | N | 5 | 22 | HLA class II | ELISPOT | (Peng et al., 2020) |
| PNNTASWFTALTQHG | N | 46 | 60 | HLA class II | ICS | (Heide et al., 2021) |
| PQNQRNAPRITFGGP | N | 6 | 20 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| PRWYFYYLGTGPEAG | N | 106 | 120 | DPB1*02:01/DQA1*05:01/DQB1*02:01/DQA1*05:01/DQB1*03:01/DQA1*03:01/DQB1*03:02/DQA1*01:01/DQB1*05:01/DQA1*01:02/DQB1*06:02/DRB1*01:01/DRB1*04:01/DRB1*04:05/DRB1*07:01/DRB1*08:02/DRB1*09:01/DRB1*11:01/DRB1*12:01/DRB1*15:01/DRB3*01:01/DRB3*02:02/DRB5*01:01/DRB1*01:01/DRB1*11:01/DQB1*05:01/DQB1*05:03/DQB1*02:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| PSASAFFGMSRIGMEVTPS | N | 309 | 327 | HLA class II | ELISA | (Verhagen et al., 2021) |
| PSGTWLTYTGAIKLD | N | 326 | 340 | DQB1*06:03/DRB1*15:01/DRB1*07:01/DRB1*01:02 | ICS/AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020; Heide et al., 2021) |
| QASSRSSSRSRNSSR | N | 181 | 195 | HLA class II | ICS | (Heide et al., 2021) |
| QELIRQGTDYKHWPQ | N | 289 | 303 | HLA class II | ELISA | (Verhagen et al., 2021) |
| QELIRQGTDYKHWPQIAQF | N | 289 | 307 | HLA class II | ELISA | (Verhagen et al., 2021) |
| QELIRQGTDYKHWPQIAQFA | N | 289 | 308 | DRB4*01:01 | multimer staining | (Johansson et al., 2021) |
| QFAPSASAFFGMSRI | N | 306 | 320 | DRB1*07:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| QKKQQTVTLLPAADL | N | 386 | 400 | DRB1*01:02 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| QQGQTVTKKSAAEAS | N | 241 | 255 | HLA class II | ICS | (Heide et al., 2021) |
| QQTVTLLPAADLDDF | N | 389 | 403 | HLA class II | ELISA | (Verhagen et al., 2021) |
| QRNAPRITFGGPSDSTGSN | N | 9 | 27 | HLA class II | ELISA | (Verhagen et al., 2021) |
| QTQGNFGDQELIRQG | N | 281 | 295 | HLA class II | ICS | (Heide et al., 2021) |
| QTQGNFGDQELIRQGTDYKH | N | 281 | 300 | DRB4*01:01 | multimer staining | (Johansson et al., 2021) |
| QVILLNKHIDAYKTF | N | 349 | 363 | HLA class II | ELISA/AIM | (Zhao et al., 2021; Verhagen et al., 2021) |
| RATRRIRGGDGKMKD | N | 89 | 103 | HLA class II | ELISA | (Verhagen et al., 2021) |
| RATRRIRGGDGKMKDLSPRW | N | 89 | 108 | DRB5*01:01 | multimer staining | (Johansson et al., 2021) |
| RLNQLESKMSGKGQQ | N | 226 | 240 | HLA class II | ICS | (Heide et al., 2021) |
| RMAGNGGDAALALLL | N | 209 | 223 | HLA class II | ELISA | (Verhagen et al., 2021) |
| RMAGNGGDAALALLLLDRL | N | 209 | 227 | HLA class II | ELISA | (Verhagen et al., 2021) |
| RNSSRNSTPGSSKRT | N | 191 | 205 | HLA class II | ICS | (Heide et al., 2021) |
| RPQGLPNNTASWFTA | N | 41 | 55 | HLA class II | ICS | (Heide et al., 2021) |
| RPQGLPNNTASWFTALTQHG | N | 41 | 60 | DRB1*04:01 | multimer staining | (Johansson et al., 2021) |
| RQGTDYKHWPQIAQFAPSA | N | 293 | 311 | HLA class II | ELISA | (Verhagen et al., 2021) |
| RQKKQQTVTLLPAADLDDFS | N | 385 | 404 | DRB1*01:01 | multimer staining | (Johansson et al., 2021) |
| RRGPEQTQGNFGDQE | N | 276 | 290 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| RSKQRRPQGLPNNTA | N | 36 | 50 | HLA class II | ICS | (Heide et al., 2021) |
| RWYFYYLGTGPEAGL | N | 107 | 121 | DRB1*11:01/DRB3*02:02 | ELISPOT/ICS/AIM/ELISA | (Titov et al., 2022; Nelde et al., 2021; Rammensee et al., 2021) |
| SAFFGMSRIGMEVTPSGTW | N | 312 | 330 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| SDSTGSNQNGERSGA | N | 21 | 35 | HLA class II | ICS | (Heide et al., 2021) |
| SNQNGERSGARSKQR | N | 26 | 40 | HLA class II | ICS | (Heide et al., 2021) |
| SPARMAGNGGDAALA | N | 206 | 220 | HLA class II | ICS | (Heide et al., 2021) |
| SPRWYFYYLGTGPEA | N | 105 | 119 | HLA class II | ELISA | (Verhagen et al., 2021) |
| SPRWYFYYLGTGPEAGLPY | N | 105 | 123 | HLA class II | ELISA | (Verhagen et al., 2021) |
| SRGGSQASSRSSSRS | N | 176 | 190 | HLA class II | ICS | (Heide et al., 2021) |
| SSKRTSPARMAGNGG | N | 201 | 215 | HLA class II | ICS | (Heide et al., 2021) |
| SSSRSRNSSRNSTPG | N | 186 | 200 | HLA class II | ICS | (Heide et al., 2021) |
| SWFTALTQHGKEDLK | N | 51 | 65 | DQA1*05:01/DQB1*02:01/DPA1*01:03/DPB1*04:01/DQB1*03:01/DQA1*03:01/DQB1*03:02/DQA1*01:02/DQB1*06:02/DRB1*01:01/DRB1*04:01/DRB1*04:05/DRB1*07:01/DRB1*08:02/DRB1*09:01/DRB1*11:01/DRB1*12:01/DRB1*15:01/DRB3*02:02/DRB4*01:01/DRB5*01:01/DRB1*15:01/DQB1*06:02 | ICS | (Le Bert et al., 2020; Heide et al., 2021) |
| TASWFTALTQHGKEDLKFPR | N | 49 | 68 | DRB1*04:01/DRB5*01:01 | multimer staining | (Johansson et al., 2021) |
| TDYKHWPQIAQFAPS | N | 296 | 310 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| TEPKKDKKKKADETQ | N | 366 | 380 | HLA class II | ICS | (Heide et al., 2021) |
| TFGGPSDSTGSNQNG | N | 16 | 30 | DQB1*03:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| TKAYNVTQAFGRRGPEQTQG | N | 265 | 284 | DRB1*07:01/DRB5*01:01 | multimer staining | (Johansson et al., 2021) |
| TLPKGFYAEGSRGGS | N | 166 | 180 | HLA class II | ICS | (Heide et al., 2021) |
| TNSSPDDQIGYYRRA | N | 76 | 90 | HLA class II | ICS | (Heide et al., 2021) |
| TPKDHIGTRNPANNA | N | 141 | 155 | HLA class II | ICS | (Heide et al., 2021) |
| TQAFGRRGPEQTQGN | N | 271 | 285 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| TRRIRGGDGKMKDLS | N | 91 | 105 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| TVTLLPAADLDDFSK | N | 391 | 405 | DRB1*01:02/DQB1*05:03 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| TWLTYTGAIKLDDKD | N | 329 | 343 | HLA class II | ELISA | (Verhagen et al., 2021) |
| TWLTYTGAIKLDDKDPNF | N | 329 | 346 | HLA class II | ELISPOT | (Peng et al., 2020) |
| TWLTYTGAIKLDDKDPNFKD | N | 329 | 348 | DRB5*01:01/DRB1*07:01/DRB1*03:01 | multimer staining | (Johansson et al., 2021) |
| VTKKSAAEASKKPRQ | N | 246 | 260 | HLA class II | ICS | (Heide et al., 2021) |
| WLTYTGAIKL | N | 330 | 339 | HLA class II | ICS | (Jin et al., 2021) |
| WPQIAQFAPSASAFF | N | 301 | 315 | DQB1*02:02/DRB1*15:01/DRB1*07:01/DRB1*04:04/DQB1*05:03 | ICS/AIM | (Tarke et al., 2021; Le Bert et al., 2020; Heide et al., 2021) |
| YKHWPQIAQFAPSAS | N | 298 | 312 | DR | ELISPOT/ICS | (Nelde et al., 2021) |
| YKTFPPTEPK | N | 360 | 369 | HLA class II | ICS | (Jin et al., 2021) |
| YTGAIKLDDKDPNFK | N | 333 | 347 | HLA class II | ELISA | (Verhagen et al., 2021) |
| YYLGTGPEAGLPYGA | N | 111 | 125 | HLA class II | ICS | (Heide et al., 2021) |
| YYRRATRRIRG | N | 86 | 96 | DRB1*11:01 | ICS | (Heide et al., 2021) |
| YYRRATRRIRGGDGK | N | 86 | 100 | DQA1*05:01/DQB1*03:01/DRB1*01:01/DRB1*04:01/DRB1*04:05/DRB1*07:01/DRB1*08:02/DRB1*09:01/DRB1*12:01/DRB1*15:01/DRB3*01:01/DRB3*02:02/DRB4*01:01/DRB5*01:01/DRB1*01:01/DRB1*13:01/DRB1*14:06 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| YYRRATRRIRGGDGKMK | N | 86 | 102 | DRB1*11:01 | AIM | (Pogorelyy et al., 2022) |
| AYCCNIVNVSLVKPS | E | 41 | 55 | HLA class II | ICS | (Heide et al., 2021) |
| FLAFVVFLLVTLAIL | E | 20 | 34 | DRB1 | ELISPOT | (Prakash et al., 2021) |
| FLLVTLAILTALRLC | E | 26 | 40 | DRB1 | ICS/ELISPOT | (Prakash et al., 2021; Heide et al., 2021) |
| FYVYSRVKNLNSSRV | E | 56 | 70 | DRB1*01:01/DRB1*04:01/DRB1*15:01/DR11/DR | multimer staining/ICS/ELISPOT | (Poluektov et al., 2021; Nelde et al., 2021; Heide et al., 2021; Rammensee et al., 2021) |
| IVNVSLVKPSFYVYS | E | 46 | 60 | HLA class II | ICS | (Heide et al., 2021) |
| LAILTALRLCAYCCN | E | 31 | 45 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| LIVNSVLLFL | E | 12 | 21 | HLA class II | ICS | (Jin et al., 2021) |
| LVKPSFYVYSRVKNL | E | 51 | 65 | DPB1*02:01/DPA1*01:03/DPB1*04:01/DQA1*05:01/DQB1*03:01/DQA1*01:02/DQB1*06:02/DRB1*01:01/DRB1*04:01/DRB1*04:05/DRB1*07:01/DRB1*08:02/DRB1*09:01/DRB1*11:01/DRB1*12:01/DRB1*13:02/DRB1*15:01/DRB3*01:01/DRB3*02:02/DRB4*01:01/DRB5*01:01/DRB1*11:01/DRB1*01:01 | ICS | (Heide et al., 2021) |
| MYSFVSEETGTLIVN | E | 1 | 15 | HLA class II | ICS | (Heide et al., 2021) |
| RVKNLNSSRVPDLLV | E | 61 | 75 | HLA class II | ICS | (Heide et al., 2021) |
| SEETGTLIVNSVLLF | E | 6 | 20 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| SFYVYSRVKNLNSSRVPD | E | 55 | 72 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| VNSVLLFLAF | E | 14 | 23 | HLA class II | ICS | (Jin et al., 2021) |
| ANVYLKHGGGVAGAL | pp1a | 243 | 257 | HLA class II | ICS/AIM | (Eggenhuizen et al., 2021) |
| LKHGGGVAGALNKAT | pp1a | 247 | 261 | HLA class II | ICS | (Eggenhuizen et al., 2021) |
| YLKHGGGVAGALNKA | pp1a | 246 | 260 | HLA class II | ICS/AIM | (Eggenhuizen et al., 2021) |
| ADAVIKTLQPVSELL | pp1ab | 876 | 890 | DRB1*14:01 | AIM | (Tarke et al., 2021) |
| AITILDGISQYSLRL | pp1ab | 566 | 580 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| AMRNAGIVGV | pp1ab | 4587 | 4596 | HLA class II | ICS | (Jin et al., 2021) |
| ASRELKVTFFPDLNG | pp1ab | 1951 | 1965 | DQB1*05:03 | AIM | (Tarke et al., 2021) |
| AVITREVGFVVPGLP | pp1ab | 2856 | 2870 | HLA class II | AIM | (Tarke et al., 2021) |
| AVMSLKEGQINDMIL | pp1ab | 7056 | 7070 | HLA class II | AIM | (Tarke et al., 2021) |
| AVTANVNALLSTDGN | pp1ab | 5091 | 5105 | HLA class II | AIM | (Tarke et al., 2021) |
| CCHLAKALNDFSNSG | pp1ab | 3231 | 3245 | HLA class II | AIM | (Tarke et al., 2021) |
| CTFLLNKEMYLKLRS | pp1ab | 3181 | 3195 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| DAFKLNIKLLGVGGK | pp1ab | 3836 | 3850 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| DNFKFVCDNIKFADD | pp1ab | 1926 | 1940 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| DTRYVLMDGSIIQFP | pp1ab | 2951 | 2965 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| DVDTDFVNEFYAYLR | pp1ab | 5128 | 5142 | HLA class II | ELISPOT | (Swadling et al., 2022) |
| DVFHLYLQYIRKLHD | pp1ab | 5271 | 5285 | DRB1*13:02/DRB1*04:04 | AIM | (Tarke et al., 2021) |
| EAARYMRSLKVPATV | pp1ab | 1461 | 1475 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| EEIAIILASFSASTS | pp1ab | 471 | 485 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| EFYAYLRKHFSMMIL | pp1ab | 5136 | 5150 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| EIIKSQDLSVVSKVV | pp1ab | 6756 | 6770 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| ELHLSWEVGKPRPPL | pp1ab | 5486 | 5500 | HLA class II | AIM | (Tarke et al., 2021) |
| ENLLLYIDINGNLHP | pp1ab | 1251 | 1265 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| ESDDYIATNGPLKVG | pp1ab | 1086 | 1100 | HLA class II | AIM | (Tarke et al., 2021) |
| ESPFVMMSAPPAQYE | pp1ab | 1801 | 1815 | DRB1 | ELISPOT | (Prakash et al., 2021) |
| FDAYVNTFSSTFNVP | pp1ab | 2591 | 2605 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| FGEYSHVVAFNTLLF | pp1ab | 3071 | 3085 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| FGLVAEWFLAYILFT | pp1ab | 2321 | 2335 | DRB1*12:01/DQB1*05:03 | AIM | (Tarke et al., 2021) |
| FLHFLPRVFSAVGNI | pp1ab | 2881 | 2895 | DRB1*15:01 | AIM | (Tarke et al., 2021) |
| FNICQAVTANVNALL | pp1ab | 5086 | 5100 | DRB1*14:01/DQB1*03:01 | AIM | (Tarke et al., 2021) |
| FSNSGSDVLYQPPQT | pp1ab | 3241 | 3255 | DQB1*06:02 | AIM | (Tarke et al., 2021) |
| FTGYRVTKNSKVQIG | pp1ab | 5506 | 5520 | DRB1*07:01 | AIM | (Tarke et al., 2021) |
| FTSLEIPRRNVATLQ | pp1ab | 5911 | 5925 | HLA class II | ELISPOT | (Swadling et al., 2022) |
| FVSLAIDAYPLTKHP | pp1ab | 5251 | 5265 | DQB1*03:02/DQB1*06:04/DRB1*15:01/DQB1*02:02 | AIM | (Tarke et al., 2021) |
| GETFVTHSKGLYRKC | pp1ab | 706 | 720 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| GLVASIKNFKSVLYY | pp1ab | 5166 | 5180 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| GPPGTGKSHFAIGLA | pp1ab | 282 | 296 | HLA class II | ICS/AIM | (Eggenhuizen et al., 2021) |
| GSLIYSTAALGVLMS | pp1ab | 2241 | 2255 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| GYKKPASRELKVTFF | pp1ab | 1946 | 1960 | HLA class II | AIM | (Tarke et al., 2021) |
| HCANFNVLFSTVFPP | pp1ab | 4701 | 4715 | DQB1*06:02/DRB1*07:01/DQB1*02:02 | AIM | (Tarke et al., 2021) |
| HTTDPSFLGRYMSAL | pp1ab | 1636 | 1650 | HLA class II | AIM | (Tarke et al., 2021) |
| IAATRGATVVIGTSK | pp1ab | 4971 | 4985 | DRB1*07:01/DQB1*03:03 | AIM | (Tarke et al., 2021) |
| IATNGPLKVGGSCVL | pp1ab | 1091 | 1105 | DRB1*13:02 | AIM | (Tarke et al., 2021) |
| IDAYPLTKHPNQEYA | pp1ab | 5256 | 5270 | HLA class II | AIM | (Tarke et al., 2021) |
| IQWMVMFTPLVPFWI | pp1ab | 3126 | 3140 | DRB1*04:04/DRB1*07:01/DQB1*02:02 | AIM | (Tarke et al., 2021) |
| ISPYNSQNAVASKIL | pp1ab | 5836 | 5850 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| ISSFKWDLTAFGLVA | pp1ab | 2311 | 2325 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| KEGQINDMILSLLSK | pp1ab | 7061 | 7075 | HLA class II | AIM | (Tarke et al., 2021) |
| KGGKIVNNWLKQLIK | pp1ab | 2761 | 2775 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| KHFYWFFSNYLKRRV | pp1ab | 3151 | 3165 | DRB1*15:01 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| KLLKSIAATRGATVV | pp1ab | 4966 | 4980 | DRB1*07:01/DQB1*03:03 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| KSAFYILPSIISNEK | pp1ab | 1350 | 1364 | DRB1 | ELISPOT | (Prakash et al., 2021) |
| KTDGTLMIERFVSLA | pp1ab | 5241 | 5255 | HLA class II | AIM | (Tarke et al., 2021) |
| KVTFFPDLNGDVVAI | pp1ab | 1956 | 1970 | DQB1*05:03 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| LCLFLLPSLATVAYF | pp1ab | 3636 | 3650 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| LDAYNMMISAGFSLW | pp1ab | 6420 | 6434 | DRB1 | ELISPOT | (Prakash et al., 2021) |
| LDDFVEIIKSQDLSV | pp1ab | 6751 | 6765 | DR | ELISPOT | (Nelde et al., 2021) |
| LEASFNYLKSPNFSK | pp1ab | 2211 | 2225 | DRB1*01:01/DRB1*04:01/DRB1*15:01 | multimer staining/ELISPOT | (Poluektov et al., 2021; Mateus et al., 2020) |
| LFVAAIFYLITPVHV | pp1ab | 2781 | 2795 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| LIVTALRANSAVKLQ | pp1ab | 4126 | 4140 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| LLVLVQSTQWSLFFF | pp1ab | 3591 | 3605 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| LMIERFVSLAIDAYP | pp1ab | 5246 | 5260 | DQB1*02:02/DRB1*15:01/DRB1*13:02/DRB1*10:01/DRB1*07:01/DRB1*04:04/DRB1*01:01/DQB1*06:04/DQB1*05:01/DQB1*04:02/DQB1*03:02 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| LMIERFVSLAIDAYPLTK | pp1ab | 5246 | 5263 | HLA class II | AIM | (Piadel et al., 2022) |
| LNQLTGYKKPASREL | pp1ab | 1941 | 1955 | HLA class II | AIM | (Tarke et al., 2021) |
| LPNDDTLRVEAFEYY | pp1ab | 1621 | 1635 | DQB1*03:02 | AIM | (Tarke et al., 2021) |
| LQGPPGTGKSHFAIG | pp1ab | 5612 | 5626 | HLA class II | ICS | (Eggenhuizen et al., 2021) |
| LRAKHYVYIGDPAQL | pp1ab | 5715 | 5729 | HLA class II | ELISPOT | (Swadling et al., 2022) |
| LRKHFSMMILSDDAV | pp1ab | 5141 | 5155 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| LTQYNRYLALYNKYK | pp1ab | 3201 | 3215 | DRB1*15:01 | AIM | (Tarke et al., 2021) |
| LVAEWFLAYILFTRFFYV | pp1ab | 2323 | 2340 | HLA class II | AIM | (Piadel et al., 2022) |
| MAAYVDNSSLTIKKP | pp1ab | 2096 | 2110 | DQB1*05:03 | AIM | (Tarke et al., 2021) |
| MFTPLVPFWITIAYI | pp1ab | 3131 | 3145 | DRB1*15:01 | AIM | (Tarke et al., 2021) |
| NELSRVLGLKTLATH | pp1ab | 2111 | 2125 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| NHNFLVQAGNVQLRV | pp1ab | 3326 | 3340 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| NHTKKWKYPQVNGLT | pp1ab | 1651 | 1665 | HLA class II | AIM | (Tarke et al., 2021) |
| NKDFYDFAVSKGFFK | pp1ab | 4808 | 4822 | HLA class II | ELISPOT | (Swadling et al., 2022) |
| NLYDKLVSSFLEMKS | pp1ab | 1181 | 1195 | DRB1*14:01/DQB1*05:02 | AIM | (Tarke et al., 2021) |
| NMFITREEAIRHVRA | pp1ab | 5996 | 6010 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| NRYFRLTLGVYDYLV | pp1ab | 3801 | 3815 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| NTLLFLMSFTVLCLT | pp1ab | 3081 | 3095 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| NTVKSVGKFCLEASF | pp1ab | 2201 | 2215 | HLA class II | AIM | (Tarke et al., 2021) |
| NVLFSTVFPPTSFGP | pp1ab | 4706 | 4720 | DQB1*02:02 | AIM | (Tarke et al., 2021) |
| NVNRFNVAITRAKVG | pp1ab | 5881 | 5895 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| PDILRVYANLGERVR | pp1ab | 4561 | 4575 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| PDLNGDVVAIDYKHY | pp1ab | 1961 | 1975 | HLA class II | AIM | (Tarke et al., 2021) |
| PLMYKGLPWNVVRIK | pp1ab | 6076 | 6090 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| PLNSIIKTIQPRVEK | pp1ab | 276 | 290 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| PNFSKLINIIIWFLL | pp1ab | 2221 | 2235 | DRB1*15:01/DRB1*07:01 | AIM | (Tarke et al., 2021) |
| PNMLRIMASLVLARK | pp1ab | 5019 | 5033 | DRB1 | ELISPOT | (Prakash et al., 2021) |
| PRPPLNRNYVFTGYR | pp1ab | 5496 | 5510 | HLA class II | AIM | (Tarke et al., 2021) |
| PVYSFLPGVYSVIYL | pp1ab | 3096 | 3110 | DRB1*15:01 | AIM | (Tarke et al., 2021) |
| QDALFAYTKRNVIPT | pp1ab | 4916 | 4930 | HLA class II | AIM | (Tarke et al., 2021) |
| QKYSTLQGPPGTGKS | pp1ab | 275 | 289 | HLA class II | ICS/AIM | (Eggenhuizen et al., 2021) |
| QNCVLKLKVDTANPK | pp1ab | 3346 | 3360 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| QTFFKLVNKFLALCA | pp1ab | 676 | 690 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| RAMPNMLRIMASLVL | pp1ab | 5016 | 5030 | DRB1*15:01/DQB1*06:02 | AIM | (Tarke et al., 2021) |
| REEAIRHVRAWIGFD | pp1ab | 6001 | 6015 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| RENNRVVISSDVLVN | pp1ab | 7081 | 7095 | DRB1*07:01/DQB1*02:02 | AIM | (Tarke et al., 2021) |
| RFYFYTSKTTVASLI | pp1ab | 1421 | 1435 | DRB1*14:01/DRB1*15:02/DQB1*06:01 | AIM | (Tarke et al., 2021) |
| RIKIVQMLSDTLKNL | pp1ab | 6088 | 6102 | DRB1 | ELISPOT | (Prakash et al., 2021) |
| RRCPAEIVDTVSALVY | pp1ab | 5766 | 5781 | HLA class II | AIM | (Piadel et al., 2022) |
| RVESSSKLWAQCVQL | pp1ab | 3880 | 3894 | HLA class II | ICS | (Le Bert et al., 2020) |
| RYLALYNKYKYFSGA | pp1ab | 3206 | 3220 | DRB1*15:01 | AIM | (Tarke et al., 2021) |
| SDVLYQPPQTSITSA | pp1ab | 3246 | 3260 | HLA class II | AIM | (Tarke et al., 2021) |
| SEFSSLPSYAAFATA | pp1ab | 3948 | 3962 | DRB1*01:01/DRB1*04:01/DRB1*15:01 | multimer staining | (Poluektov et al., 2021) |
| SEMVMCGGSLYVKPG | pp1ab | 5056 | 5070 | HLA class II | AIM | (Tarke et al., 2021) |
| SFLAHIQWMVMFTPL | pp1ab | 3121 | 3135 | DRB1*15:01/DQB1*06:02 | AIM | (Tarke et al., 2021) |
| SFLGRYMSALNHTKK | pp1ab | 1641 | 1655 | DRB1*04:04 | AIM | (Tarke et al., 2021) |
| SGHNLAKHCLHVVGP | pp1ab | 1106 | 1120 | HLA class II | AIM | (Tarke et al., 2021) |
| SHNIALIWNVKDFMS | pp1ab | 2706 | 2720 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| SHRFYRLANECAQVL | pp1ab | 5041 | 5055 | DRB1*08:01/DRB1*01:01 | AIM | (Tarke et al., 2021) |
| SIVAGGIVAIVVTCL | pp1ab | 3046 | 3060 | DQB1*04:02/DQB1*03:02 | AIM | (Tarke et al., 2021) |
| SKLWAQCVQLHNDIL | pp1ab | 3885 | 3899 | HLA class II | ICS | (Le Bert et al., 2020) |
| SLFFFLYENAFLPFA | pp1ab | 3601 | 3615 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| SLLMPILTLTRALTA | pp1ab | 4631 | 4645 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| SPLYAFASEAARVVR | pp1ab | 531 | 545 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| TFTRSTNSRIKASMP | pp1ab | 2181 | 2195 | DRB1*14:01 | AIM | (Tarke et al., 2021) |
| TIAYIICISTKHFYW | pp1ab | 3141 | 3155 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| TLRVEAFEYYHTTDP | pp1ab | 1626 | 1640 | DQB1*05:03 | AIM | (Tarke et al., 2021) |
| TLVYKVYYGNALDQA | pp1ab | 3716 | 3730 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| TNSRIKASMPTTIAK | pp1ab | 2186 | 2200 | DRB1*07:01/DRB1*04:04 | AIM | (Tarke et al., 2021) |
| TPSFKKGAKLLHKPI | pp1ab | 1976 | 1990 | HLA class II | AIM | (Tarke et al., 2021) |
| TQLCQYLNTLTLAVP | pp1ab | 6846 | 6860 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| TSHKLVLSVNPYVCN | pp1ab | 5361 | 5375 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| TSLLVLVQSTQWSLF | pp1ab | 3589 | 3603 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| VLKKLKKSLNVAKSE | pp1ab | 3976 | 3990 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| VLSFCAFAVDAAKAY | pp1ab | 4266 | 4280 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| VNARLRAKHYVYIGD | pp1ab | 5711 | 5725 | HLA class II | AIM | (Tarke et al., 2021) |
| VNRFNVAITRAKVGI | pp1ab | 558 | 572 | HLA class II | ICS/AIM | (Eggenhuizen et al., 2021) |
| VPGLPGTILRTTNGD | pp1ab | 2866 | 2880 | HLA class II | AIM | (Tarke et al., 2021) |
| VSALVYDNKLKAHKD | pp1ab | 452 | 466 | HLA class II | ICS/AIM | (Eggenhuizen et al., 2021) |
| VTKNSKVQIGEYTFE | pp1ab | 5511 | 5525 | HLA class II | AIM | (Tarke et al., 2021) |
| VWHVNNATNKATYKP | pp1ab | 1991 | 2005 | HLA class II | AIM | (Tarke et al., 2021) |
| WDLTAFGLVAEWFLA | pp1ab | 2316 | 2330 | DQB1*05:03 | AIM | (Tarke et al., 2021) |
| YCIDGALLTKSSEYK | pp1ab | 1846 | 1860 | DRB1*15:02 | AIM | (Tarke et al., 2021) |
| YLTFYLTNDVSFLAH | pp1ab | 3111 | 3125 | DRB1*14:01/DRB1*15:01/DRB1*16:01/DQB1*05:02 | AIM | (Tarke et al., 2021) |
| YMSALNHTKKWKYPQ | pp1ab | 1646 | 1660 | HLA class II | AIM | (Tarke et al., 2021) |
| YREAACCHLAKALND | pp1ab | 3226 | 3240 | HLA class II | AIM | (Tarke et al., 2021) |
| YPKCDRAMPNMLRIM | pp1ab | 5011 | 5025 | HLA class II | AIM | (Tarke et al., 2021) |
| AENSVAYSNNSIAIP | S | 701 | 715 | DRB1*15:01/DQB1*03:01 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| AGFIKQYGDCLGDIA | S | 831 | 845 | DQB1*05:03 | AIM/ICS | (Tarke et al., 2021; Zhang et al., 2022; Tarke et al., 2022) |
| AIPTNFTISVTTEILPVSMT | S | 713 | 732 | DRB1*07:01 | multimer staining | (Johansson et al., 2021) |
| ALLAGTITSGWTFGA | S | 876 | 890 | DQB1*06:02 | AIM | (Tarke et al., 2021) |
| ALQIPFAMQMAYRFNGIGV | S | 893 | 911 | HLA class II | ELISA | (Verhagen et al., 2021) |
| APHGVVFLHVTYVPA | S | 1056 | 1070 | DRB1*12:01 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| AQALNTLVKQLSSNF | S | 956 | 970 | HLA class II | AIM/ELISPOT | (Mateus et al., 2020; Tarke et al., 2022) |
| AQYTSALLAGTITSG | S | 871 | 885 | DQB1*06:02 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020; Tarke et al., 2022) |
| ARDLICAQKFNGLTV | S | 846 | 860 | HLA class II | AIM | (Tarke et al., 2021) |
| ASFSTFKCYGVSPTKLN | S | 372 | 388 | DRB1*15:02/DPA1*01:03/DPB1*06:01 | ELISPOT | (Woldemeskel et al., 2021) |
| ASVYAWNRKRISN | S | 348 | 360 | DR | ICS/ELISPOT | (Rammensee et al., 2021) |
| AYSNNSIAIPTNFTI | S | 706 | 720 | DQB1*03:01 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020; Tarke et al., 2022) |
| CAQKFNGLTVLPPLL | S | 851 | 865 | DQB1*06:02/DRB1*16:01/DQB1*05:02 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| CEFQFCNDPFLGVYY | S | 131 | 145 | DQB1*05:02/DQB1*05:03 | AIM/ELISPOT/ICS | (Tarke et al., 2021; Mateus et al., 2020; Zhang et al., 2022; Tarke et al., 2022) |
| CPFGEVFNATRFASV | S | 336 | 350 | DRB1*07:01/DRB1*13:01/DQB1*06:03 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| CPFGEVFNATRFASVYAWNR | S | 336 | 355 | HLA class II | proliferation | (Low et al., 2021) |
| CSNLLLQYGSFCTQL | S | 749 | 763 | DRB1*15:01 | AIM,ELISA | (Panikkar et al., 2022; Li et al., 2021; Loyal et al., 2021) |
| CTFEYVSQPFLMDLE | S | 166 | 180 | DQB1*02:01/DRB1*16:01/DRB1*07:01/DQB1*05:03/DQB1*05:02/DQB1*02:02 | AIM,ICS,ELISPOT | (Tarke et al., 2021; Mateus et al., 2020; Tarke et al., 2022; Le Bert et al., 2021) |
| CTFEYVSQPFLMDLEGK | S | 166 | 182 | DPA1*01:03/DPB1*04:01 | AIM | (Pogorelyy et al., 2022) |
| CTLKSFTVEKGIYQT | S | 301 | 315 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| CVADYSVLYNSASFS | S | 361 | 375 | DQB1*06:02/DQB1*05:03 | AIM | (Tarke et al., 2021) |
| DCTMYICGDSTECSN | S | 737 | 751 | HLA class II | ELISA | (Verhagen et al., 2021) |
| DKVEAEVQIDRLITGRLQSL | S | 985 | 1004 | DRB1*03:01 | multimer staining | (Johansson et al., 2021) |
| DSFKEELDKYFKNHT | S | 1146 | 1160 | HLA class II | AIM | (Tarke et al., 2022) |
| DSKTQSLLIVNNATN | S | 111 | 125 | HLA class II | AIM | (Tarke et al., 2021) |
| DSKVGGNYNYLYRLFRK | S | 442 | 458 | DRB1*11:01 | ELISPOT | (Woldemeskel et al., 2021) |
| DSLSSTASALGKLQDVV | S | 936 | 952 | HLA class II | ICS | (Bartolo et al., 2021) |
| DSTECSNLLLQYGSF | S | 745 | 759 | HLA class II | ELISA | (Li et al., 2021) |
| DSTECSNLLLQYGSFCTQLN | S | 745 | 764 | DRB1*15:01 | multimer staining | (Johansson et al., 2021) |
| ECDIPIGAGICASYQ | S | 661 | 675 | HLA class II | ELISA/ELISPOT | (Mateus et al., 2020; Verhagen et al., 2021) |
| EFVFKNIDGYFKIYS | S | 191 | 205 | DRB1*14:01/DRB1*15:01/DQB1*05:03 | AIM | (Tarke et al., 2021; Tarke et al., 2022) |
| EIRASANLAATKMSECVLGQ | S | 1017 | 1036 | DRB1*04:01/DRB1*04:04 | multimer staining | (Johansson et al., 2021) |
| EIYQAGSTPCNGVEG | S | 471 | 485 | HLA class II | AIM/ICS | (Tarke et al., 2021; Zhang et al., 2022) |
| EKSNIIRGWIFGTTL | S | 96 | 110 | DRB1*15:01 | AIM | (Tarke et al., 2021) |
| ELDKYFKNHTSPDVD | S | 1151 | 1165 | HLA class II | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| ELLHAPATVCGPKKSTNLVK | S | 516 | 535 | HLA class II | proliferation | (Low et al., 2021) |
| ENQKLIANQFNSAIGKI | S | 918 | 934 | DRB3*02:02 | ELISPOT | (Woldemeskel et al., 2021) |
| EPQIITTDNTFVSGN | S | 1111 | 1125 | HLA class II | AIM | (Tarke et al., 2022) |
| EVRQIAPGQTGKIADYNYKL | S | 406 | 425 | HLA class II | proliferation | (Low et al., 2021) |
| FGEVFNATRFASVYA | S | 338 | 352 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| FGGFNFSQILPDPSK | S | 797 | 811 | HLA class II | ELISPOT | (Zhao et al., 2021) |
| FGGFNFSQILPDPSKPSKR | S | 797 | 815 | HLA class II | ELISA | (Verhagen et al., 2021) |
| FGTTLDSKTQSLLIV | S | 106 | 120 | HLA class II | AIM | (Tarke et al., 2021) |
| FIEDLLFNKVTLADA | S | 817 | 831 | HLA class II | AIM | (Loyal et al., 2021) |
| FIEDLLFNKVTLADAGFIKQ | S | 817 | 836 | DPB1*04:01 | multimer staining | (Johansson et al., 2021) |
| FKIYSKHTPINLVRD | S | 201 | 215 | DRB1*13:01/DRB1*07:01 | AIM/ELISPOT | (Tarke et al., 2021; Zhao et al., 2021) |
| FKIYSKHTPINLVRDLPQGF | S | 201 | 220 | DRB1*07:01/DRB3*01:01 | multimer staining | (Johansson et al., 2021) |
| FNCYFPLQSYGFQPT | S | 486 | 500 | DRB1*12:01/DQB1*05:03 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| FNCYFPLQSYGFQPTNGVGY | S | 486 | 505 | HLA class II | proliferation | (Low et al., 2021) |
| FNFNGLTGTGVLTES | S | 541 | 555 | HLA class II | ELISA/AIM/ELISPOT | (Mateus et al., 2020; Tarke et al., 2022; Verhagen et al., 2021) |
| FNGLTVLPPLLTDEM | S | 855 | 869 | DR | ELISPOT | (Nelde et al., 2021) |
| FQFCNDPFLGVYYHK | S | 133 | 147 | HLA class II | ELISA | (Verhagen et al., 2021) |
| FQFCNDPFLGVYYHKNNK | S | 133 | 150 | HLA class II | ELISA | (Verhagen et al., 2021) |
| FRKSNLKPFERDISTEIYQA | S | 456 | 475 | HLA class II | proliferation | (Low et al., 2021) |
| FTGCVIAWNSNNLDSKVGG | S | 429 | 447 | HLA class II | ELISA | (Verhagen et al., 2021) |
| FTVEKGIYQTSNFRV | S | 306 | 320 | DRB1*07:01 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| FVIRGDEVRQIAPGQTG | S | 400 | 416 | DQA1*05:05/DQB1*03:01 | ELISPOT | (Woldemeskel et al., 2021) |
| FVSGNCDVVIGIVNN | S | 1121 | 1135 | HLA class II | AIM | (Tarke et al., 2021) |
| FYEPQIITTDNTFVSGNCD | S | 1109 | 1127 | HLA class II | ELISA | (Verhagen et al., 2021) |
| GAAAYYVGYLQPRTF | S | 261 | 275 | HLA class II | AIM | (Tarke et al., 2022) |
| GAALQIPFAMQMAYR | S | 891 | 905 | HLA class II | AIM | (Tarke et al., 2022) |
| GAEHVNNSYECDIPIGA | S | 652 | 668 | DQA1*02:01/DQB1*02:02 | ELISPOT | (Woldemeskel et al., 2021) |
| GAGAALQIPFAMQMAYRFNG | S | 889 | 908 | DRB1*01:01/DRB1*07:01/DRB1*11:04/DRB5*01:01 | multimer staining | (Johansson et al., 2021) |
| GAISSVLNDILSRLD | S | 971 | 985 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| GCVIAWNSNNLDSKV | S | 431 | 445 | HLA class II | ICS/AIM/ELISPOT | (Mateus et al., 2020; Tarke et al., 2022; Mahajan et al., 2021) |
| GFQPTNGVGYQPYRVVVLSF | S | 496 | 515 | HLA class II | proliferation | (Low et al., 2021) |
| GGNYNYLYRLFRKSN | S | 446 | 460 | HLA class II | ICS/AIM/ELISPOT | (Mateus et al., 2020; Mahajan et al., 2021) |
| GGNYNYLYRLFRKSNLKPFE | S | 446 | 465 | HLA class II | proliferation | (Low et al., 2021) |
| GINASVVNIQKEIDR | S | 1171 | 1185 | HLA class II | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| GINITRFQTLLALHRSY | S | 232 | 248 | HLA class II | AIM | (Dykema et al., 2021) |
| GIVNNTVYDPLQPEL | S | 1131 | 1145 | DQB1*03:02/DQB1*02:02 | AIM | (Tarke et al., 2021) |
| GIYQTSNFRVQPTES | S | 311 | 325 | HLA class II | AIM/ELISPOT | (Mateus et al., 2020; Tarke et al., 2022) |
| GKIADYNYKLPDDFT | S | 416 | 430 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| GKIADYNYKLPDDFTGCVIA | S | 416 | 435 | HLA class II | proliferation | (Low et al., 2021) |
| GKLQDVVNQNAQALN | S | 946 | 960 | HLA class II | ICS/AIM | (Mahajan et al., 2021) |
| GKQGNFKNLREFVFK | S | 181 | 195 | HLA class II | AIM | (Tarke et al., 2021) |
| GLTVLPPLLTDEMIAQYTSA | S | 857 | 876 | DRB1*03:01 | multimer staining | (Johansson et al., 2021) |
| GNYNYLYRLFRKSNL | S | 447 | 461 | HLA class II | ELISA | (Li et al., 2021) |
| GNYNYLYRLFRKSNLKPFER | S | 447 | 466 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| GPKKSTNLVKNKCVNFNFNG | S | 526 | 545 | HLA class II | proliferation | (Low et al., 2021) |
| GSTPCNGVEGFNCYFPLQSY | S | 476 | 495 | HLA class II | proliferation | (Low et al., 2021) |
| GVSPTKLNDLCFTNV | S | 390 | 404 | HLA class II | ELISPOT | (Peng et al., 2020) |
| GWTAGAAAYYVGYLQ | S | 257 | 271 | HLA class II | ELISA/AIM | (Li et al., 2021) |
| GWTFGAGAALQIPFA | S | 885 | 899 | DQB1*03:01 | ELISA | (Titov et al., 2022; Verhagen et al., 2021) |
| HADQLTPTWRVYSTGSNVFQ | S | 625 | 644 | DRB1*07:01 | multimer staining | (Johansson et al., 2021) |
| HKNNKSWMESEFRVY | S | 146 | 160 | DQB1*05:03 | AIM | (Tarke et al., 2021) |
| HWFVTQRNFYEPQII | S | 1101 | 1115 | HLA class II | AIM/ELISA/CBA/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020; Tarke et al., 2022; Verhagen et al., 2021) |
| HWFVTQRNFYEPQIITTDN | S | 1101 | 1119 | HLA class II | ELISA | (Verhagen et al., 2021) |
| IDGYFKIYSKHTPIN | S | 197 | 211 | HLA class II | ELISPOT | (Zhao et al., 2021) |
| IDRLITGRLQSLQTYVTQQL | S | 993 | 1012 | DRB1*01:01/DRB1*04:04 | multimer staining | (Johansson et al., 2021) |
| IEDLLFNKVTLADAG | S | 818 | 832 | DRB3*02:02/DRB4*01:03 | ELISA | (Titov et al., 2022) |
| IGAGICASYQTQTNS | S | 666 | 680 | HLA class II | AIM | (Tarke et al., 2022) |
| IGINITRFQTLLALH | S | 231 | 245 | DRB1*07:01 | AIM/ELISPOT/ICS | (Tarke et al., 2021; Mateus et al., 2020; Zhang et al., 2022; Tarke et al., 2022) |
| ILPVSMTKTSVDCTM | S | 726 | 740 | HLA class II | AIM | (Tarke et al., 2022) |
| INITRFQTLLALHRSYLTPG | S | 233 | 252 | DRB1*04:04/DRB1*15:01/DRB5*01:01 | multimer staining | (Johansson et al., 2021) |
| IPFAMQMAYRFNGIG | S | 896 | 910 | DQB1*05:03/DRB1*12:01/DRB1*14:01/DRB1*15:01/DQB1*04:02 | AIM/ICS/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020; Tarke et al., 2022; Mahajan et al., 2021) |
| IPFAMQMAYRFNGIGVTQNV | S | 896 | 915 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| IRGWIFGTTLDSKTQ | S | 101 | 115 | HLA class II | AIM | (Tarke et al., 2021) |
| ISGINASVVNIQKEI | S | 1169 | 1183 | HLA class II | ELISA | (Titov et al., 2022) |
| ISSVLNDILSRLDKV | S | 973 | 987 | HLA class II | AIM | (Loyal et al., 2021) |
| ITRFQTLLALHRSYL | S | 235 | 249 | DR | ELISPOT/ICS | (Nelde et al., 2021) |
| IVRFPNITNLCPFGE | S | 326 | 340 | DRB1*15:01 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| IYKTPPIKDF | S | 788 | 797 | HLA class II | ICS | (Jin et al., 2021) |
| KAHFPREGVFVSNGT | S | 1086 | 1100 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| KAHFPREGVFVSNGTHWFVT | S | 1086 | 1105 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| KCVNFNFNGLTGTGVLTESN | S | 537 | 556 | DRB1*01:01 | multimer staining | (Johansson et al., 2021) |
| KEELDKYFKNHTSPD | S | 1149 | 1163 | HLA class II | ELISA | (Verhagen et al., 2021) |
| KHTPINLVRDLPQGF | S | 206 | 220 | DRB1*03:01 | AIM | (Tarke et al., 2021) |
| KLIANQFNSAIGKIQ | S | 921 | 935 | HLA class II | ELISA/AIM | (Tarke et al., 2022; Verhagen et al., 2021) |
| KLNDLCFTNVYADSF | S | 386 | 400 | DQB1*02:02/DRB1*07:01/DQB1*02:01 | AIM | (Tarke et al., 2021; Tarke et al., 2022) |
| KLNDLCFTNVYADSFVI | S | 386 | 402 | DPA1*02:01/DPB1*14:01 | ELISPOT | (Woldemeskel et al., 2021) |
| KLNDLCFTNVYADSFVIRGD | S | 386 | 405 | HLA class II | proliferation | (Low et al., 2021) |
| KNFTTAPAICHDGKAHFPRE | S | 1073 | 1092 | DRB1*03:01 | multimer staining | (Johansson et al., 2021) |
| KNTQEVFAQVKQIYK | S | 776 | 790 | HLA class II | AIM | (Tarke et al., 2021) |
| KPSKRSFIEDLLFNK | S | 811 | 825 | DQB1*05:03/DQB1*02:02 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| KRISNCVADYSVLYN | S | 356 | 370 | DQB1*02:02/DRB1*03:01/DQB1*02:01 | AIM | (Tarke et al., 2021; Tarke et al., 2022) |
| KRISNCVADYSVLYNSASFS | S | 356 | 375 | HLA class II | proliferation | (Low et al., 2021) |
| KSNIIRGWIFGTTLDSKTQS | S | 97 | 116 | DRB1*15:01 | multimer staining | (Johansson et al., 2021) |
| KVCEFQFCNDPFLGVYYHK | S | 129 | 147 | HLA class II | ELISA/CBA | (Verhagen et al., 2021) |
| KVCEFQFCNDPFLGVYYHKN | S | 129 | 148 | DPB1*04:01 | multimer staining | (Johansson et al., 2021) |
| KVFRSSVLHSTQDLF | S | 41 | 55 | HLA class II | AIM | (Tarke et al., 2022) |
| KVFRSSVLHSTQDLFLPFFS | S | 41 | 60 | DRB1*07:01 | multimer staining | (Johansson et al., 2021) |
| KYEQYIKWPWYIWLG | S | 1205 | 1219 | HLA class II | ELISA | (Li et al., 2021) |
| LDSKVGGNYNYLYRLFRKS | S | 441 | 459 | HLA class II | ELISA | (Verhagen et al., 2021) |
| LDSKVGGNYNYLYRLFRKSN | S | 441 | 460 | DRB1*11:01/DRB1*11:04 | multimer staining | (Johansson et al., 2021) |
| LGDIAARDLICAQKF | S | 841 | 855 | HLA class II | AIM | (Tarke et al., 2021) |
| LGDISGINASVVNIQ | S | 1166 | 1180 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| LGVYYHKNNKSWMES | S | 141 | 155 | HLA class II | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| LGVYYHKNNKSWMESEF | S | 141 | 157 | DRB3*02:02 | ELISPOT | (Woldemeskel et al., 2021) |
| LKPFERDISTEIYQA | S | 461 | 475 | DRB1 | AIM/multimer staining/ICS/ELISA | (Tarke et al., 2021; Prakash et al., 2021; Verhagen et al., 2021) |
| LLALHRSYLTPGDSS | S | 241 | 255 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| LLFNKVTLADAGFIK | S | 821 | 835 | DQB1*06:02 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| LLQYGSFCTQLNRAL | S | 753 | 767 | DRB1*15:01 | AIM/ELISA | (Panikkar et al., 2022; Verhagen et al., 2021; Loyal et al., 2021) |
| LLQYGSFCTQLNRALTGIAV | S | 753 | 772 | DRB1*15:01 | multimer staining | (Johansson et al., 2021) |
| LITGRLQSLQTYVTQ | S | 996 | 1010 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| LMDLEGKQGNFKNLR | S | 176 | 190 | HLA class II | AIM | (Tarke et al., 2021; Tarke et al., 2022) |
| LNEVAKNLNESLIDL | S | 1186 | 1200 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| LPDDFTGCVIAWNSNNLDSK | S | 425 | 444 | DRB1*15:01 | multimer staining | (Johansson et al., 2021) |
| LPDPSKPSKRSFIED | S | 806 | 820 | HLA class II | AIM | (Tarke et al., 2021) |
| LPFFSNVTWFHAIHV | S | 56 | 70 | DRB1*15:01/DRB1*16:01/DQB1*05:02 | AIM | (Tarke et al., 2021; Tarke et al., 2022) |
| LPLVSSQCVNLTTRTQL | S | 8 | 24 | DRB4*01:01 | ELISPOT | (Woldemeskel et al., 2021) |
| LPPLLTDEMIAQYTS | S | 861 | 875 | DQB1*04:02 | AIM | (Tarke et al., 2021) |
| LPQGFSALEPLVDLP | S | 216 | 230 | DQB1*03:03/DQB1*05:03/DQB1*02:02 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| LQPELDSFKEELDKY | S | 1141 | 1155 | HLA class II | AIM/ELISA | (Tarke et al., 2021; Tarke et al., 2022; Li et al., 2021; Verhagen et al., 2021) |
| LQSLQTYVTQQLIRA | S | 1001 | 1015 | HLA class II | AIM/ELISA | (Titov et al., 2022; Loyal et al., 2021) |
| LQSLQTYVTQQLIRAAEIRA | S | 1001 | 1020 | DRB1*15:01 | AIM/multimer staining | (Johansson et al., 2021) |
| LQTYVTQQLIRAAEI | S | 1004 | 1018 | HLA class II | ELISA | (Titov et al., 2022) |
| LSFELLHAPATVCGP | S | 513 | 527 | HLA class II | ELISA | (Verhagen et al., 2021) |
| LSFELLHAPATVCGPKKSTN | S | 513 | 532 | DRB1*01:01 | multimer staining | (Johansson et al., 2021) |
| LSRLDKVEAEVQIDR | S | 981 | 995 | HLA class II | proliferation | (Low et al., 2021) |
| LSRLDKVEAEVQIDRLITGR | S | 981 | 1000 | HLA class II | proliferation | (Low et al., 2021) |
| LTDEMIAQYTSALLA | S | 865 | 879 | DRB1*15:01 | AIM/ELISA | (Panikkar et al., 2022; Li et al., 2021) |
| LTDEMIAQYTSALLAGTITS | S | 865 | 884 | DRB1*15:01 | multimer staining | (Johansson et al., 2021) |
| LTGTGVLTESNKKFL | S | 546 | 560 | HLA class II | AIM | (Tarke et al., 2021; Tarke et al., 2022) |
| LYENQKLIANQFNSA | S | 916 | 930 | DRB1*12:01 | AIM | (Tarke et al., 2021) |
| LYNSASFSTF | S | 368 | 377 | HLA class II | ICS | (Jin et al., 2021) |
| MFVFLVLLPLVSS | S | 1 | 13 | DRB1 | ELISPOT | (Prakash et al., 2021) |
| MIAQYTSALLAGTIT | S | 869 | 883 | DRB1*15:01 | AIM/ELISA | (Panikkar et al., 2022; Li et al., 2021) |
| MTKTSVDCTMYICGD | S | 731 | 745 | HLA class II | ICS | (Zhang et al., 2022) |
| NCTFEYVSQPFLMDL | S | 165 | 179 | DPB1*04:01 | ELISA/CBA/AIM | (Panikkar et al., 2022; Verhagen et al., 2021) |
| PPAYTNSFTRGVYYP | S | 25 | 39 | HLA class II | ELISA | (Verhagen et al., 2021) |
| PPAYTNSFTRGVYYPDKVFR | S | 25 | 44 | DRB1*01:01/DRB3*01:01/DRB1*04:01/DRB1*07:01 | multimer staining | (Johansson et al., 2021) |
| PRRARSVASQSIIAYTMSLG | S | 681 | 700 | DRB1*07:01 | multimer staining | (Johansson et al., 2021) |
| PSKPSKRSFIEDLLFNKVTL | S | 809 | 828 | DPB1*04:01 | multimer staining/AIM | (Johansson et al., 2021) |
| PTNFTISVTTEILPVSM | S | 715 | 731 | DRB1*07:01 | ELISPOT | (Woldemeskel et al., 2021) |
| QALNTLVKQLSSNFG | S | 957 | 971 | HLA class II | AIM | (Loyal et al., 2021) |
| QDVNCTEVPVAIHADQLTP | S | 613 | 631 | HLA class II | ELISA | (Verhagen et al., 2021) |
| QELGKYEQYIKWPWY | S | 1201 | 1215 | HLA class II | AIM | (Tarke et al., 2021) |
| QFCNDPFLGVYHKNNK | S | 134 | 149 | HLA class II | AIM | (Dykema et al., 2021) |
| QFCNDPFLGVYYHKNNK | S | 134 | 150 | DRB1*11:01 | ELISPOT | (Woldemeskel et al., 2021) |
| QIITTDNTFVSGNCDVVIGI | S | 1113 | 1132 | DRB1*03:01/DRB1*04:01 | multimer staining | (Johansson et al., 2021) |
| QIPFAMQMAYRFNGI | S | 895 | 909 | HLA class II | ELISA/ICS | (Titov et al., 2022) |
| QLIRAAEIRASANLAATK | S | 1011 | 1028 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| QLIRAAEIRASANLAATKM | S | 1011 | 1029 | DRB1 | multimer staining/AIM/ICS | (Prakash et al., 2021) |
| QLSSNFGAISSVLND | S | 965 | 979 | HLA class II | ELISA | (Verhagen et al., 2021) |
| QMAYRFNGIGVTQNV | S | 901 | 915 | DQB1*03:01 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020; Tarke et al., 2022) |
| QNVLYENQKLIANQF | S | 913 | 927 | HLA class II | ELISA | (Verhagen et al., 2021) |
| QNVLYENQKLIANQFNSAIG | S | 913 | 932 | DRB1*11:01/DRB1*11:04/DRB1*15:01 | multimer staining | (Johansson et al., 2021) |
| QPTESIVRFPNITNL | S | 321 | 335 | HLA class II | AIM/ELISPOT | (Zhao et al., 2021; Mateus et al., 2020) |
| QPTESIVRFPNITNLCPFGE | S | 321 | 340 | DRB1*04:04/DRB1*15:01 | multimer staining | (Johansson et al., 2021) |
| QPYRVVVLSFELLHA | S | 506 | 520 | DRB1*14:01/DQB1*05:03 | AIM/ICS | (Tarke et al., 2021; Mahajan et al., 2021) |
| QPYRVVVLSFELLHAPATVC | S | 506 | 525 | HLA class II | proliferation | (Low et al., 2021) |
| QQLIRAAEIRASANL | S | 1010 | 1024 | HLA class II | ELISA | (Titov et al., 2022) |
| QRNFYEPQIITTDNT | S | 1106 | 1120 | HLA class II | AIM | (Tarke et al., 2021; Tarke et al., 2022) |
| NFGAISSVLNDILSR | S | 969 | 983 | HLA class II | AIM | (Loyal et al., 2021) |
| NFKNLREFVFKNIDGYFKIY | S | 185 | 204 | DRB5*01:01 | multimer staining | (Johansson et al., 2021) |
| NFRVQPTESIVRFPN | S | 317 | 331 | DRB1*04:01 | ELISA/AIM | (Panikkar et al., 2022; Verhagen et al., 2021) |
| NFSQILPDPSKPSKR | S | 810 | 824 | DRB1*03:01 | ELISPOT/AIM/ELISA/CBA | (Tarke et al., 2021; Zhao et al., 2021; Peng et al., 2020; Mateus et al., 2020; Verhagen et al., 2021; Loyal et al., 2021) |
| NFSQILPDPSKPSKRSFIE | S | 801 | 819 | HLA class II | ELISA | (Verhagen et al., 2021) |
| NFSQILPDPSKPSKRSFIED | S | 801 | 820 | DRB1*03:01/DRB1*04:01/DRB1*04:04 | multimer staining | (Johansson et al., 2021) |
| NGVEGFNCYFPLQSY | S | 481 | 495 | HLA class II | ICS | (Mahajan et al., 2021) |
| NGVEGFNCYFPLQSYGFQPT | S | 481 | 500 | DRB5*01:01 | multimer staining | (Johansson et al., 2021) |
| NIDGYFKIYSKHTPI | S | 196 | 210 | DRB1*07:01/DRB1*16:01/DRB1*15:01 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020; Tarke et al., 2022) |
| NIIRGWIFGTTLDSKTQ | S | 99 | 115 | DPA1*01:03 | ELISPOT | (Woldemeskel et al., 2021) |
| NKSWMESEFRVYSSA | S | 149 | 163 | HLA class II | ELISA | (Li et al., 2021) |
| NLLLQYGSFCTQLNR | S | 760 | 774 | DQB1*05:03/DRB1*15:01/DRB1*04:04 | ELISPOT/AIM | (Tarke et al., 2021; Peng et al., 2020; Mateus et al., 2020; Tarke et al., 2022) |
| NLLLQYGSFCTQLNRAL | S | 751 | 767 | DRB1*15:01 | AIM | (Pogorelyy et al., 2022) |
| NLVRDLPQGFSALEP | S | 211 | 225 | DRB1*03:01 | AIM | (Tarke et al., 2021) |
| NNATNVVIKVCEFQF | S | 121 | 135 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| NNSYECDIPIGAGIC | S | 657 | 671 | HLA class II | ELISA | (Verhagen et al., 2021) |
| NNSYECDIPIGAGICASYQ | S | 657 | 675 | HLA class II | ELISA/CBA | (Verhagen et al., 2021) |
| NPVLPFNDGVYFAST | S | 81 | 95 | HLA class II | AIM | (Tarke et al., 2021) |
| NQNAQALNTLVKQLSSNFG | S | 953 | 971 | HLA class II | ELISA | (Verhagen et al., 2021) |
| NQNAQALNTLVKQLSSNFGA | S | 953 | 972 | DRB1*01:01/DRB1*04:04/DRB1*11:01/DRB1*11:04 | multimer staining | (Johansson et al., 2021) |
| NRKRISNCVAD | S | 354 | 364 | DP | proliferation | (Low et al., 2021) |
| NTLVKQLSSNFGAISSV | S | 960 | 976 | DRB3*02:02 | ELISPOT | (Woldemeskel et al., 2021) |
| NTQEVFAQVKQIYKTPPIKD | S | 777 | 796 | DRB1*11:04/DRB5*01:01 | multimer staining | (Johansson et al., 2021) |
| NVFQTRAGCLIGAEH | S | 641 | 655 | HLA class II | AIM | (Tarke et al., 2022) |
| NVFQTRAGCLIGAEHVNNS | S | 641 | 659 | HLA class II | ELISA | (Verhagen et al., 2021) |
| NVTWFHAIHVSGTNG | S | 61 | 75 | HLA class II | ELISA/ELISPOT | (Keller et al., 2020; Verhagen et al., 2021) |
| NVVIKVCEFQFCNDP | S | 125 | 139 | HLA class II | ELISA | (Verhagen et al., 2021) |
| PAYTNSFTRGVYYPD | S | 26 | 40 | HLA class II | AIM | (Tarke et al., 2022) |
| PDDFTGCVIAWNSNN | S | 426 | 440 | HLA class II | AIM | (Tarke et al., 2022) |
| PDDFTGCVIAWNSNNLDSKV | S | 426 | 445 | HLA class II | proliferation | (Low et al., 2021) |
| PFAMQMAYRFNGIGV | S | 897 | 911 | HLA class II | ELISA | (Verhagen et al., 2021) |
| PFAMQMAYRFNGIGVTQNVL | S | 897 | 916 | DRB1*01:01/DRB1*11:01/DRB1*11:04/DRB5*01:01 | multimer staining | (Johansson et al., 2021) |
| PFFSNVTWFHAIHVS | S | 57 | 71 | HLA class II | ELISPOT | (Keller et al., 2020) |
| PFFSNVTWFHAIHVSGTNGT | S | 57 | 76 | DRB1*01:01/DRB1*07:01/DRB1*15:01 | multimer staining | (Johansson et al., 2021) |
| PFGEVFNATRFASVYAWNRK | S | 337 | 356 | DRB5*01:01/DPB1*04:01 | multimer staining | (Johansson et al., 2021) |
| PFNDGVYFASTEKSNII | S | 85 | 101 | DRB3*02:02 | ELISPOT | (Woldemeskel et al., 2021) |
| PHGVVFLHVTYVPAQEKNFT | S | 1057 | 1076 | DRB5*01:01 | multimer staining | (Johansson et al., 2021) |
| PINLVRDLPQGFSAL | S | 209 | 223 | DRB1*03:01/DRB3*01:01 | ELISA/ELISPOT | (Verhagen et al., 2021),25 |
| PINLVRDLPQGFSALEPLVD | S | 209 | 228 | DRB3*01:01 | multimer staining | (Johansson et al., 2021) |
| PLVDLPIGINITRFQTLLAL | S | 225 | 244 | DRB1*04:04 | multimer staining | (Johansson et al., 2021) |
| QTYVTQQLIRAAEIR | S | 1005 | 1019 | HLA class II | ELISA | (Titov et al., 2022) |
| QYGDCLGDIAARDLI | S | 836 | 850 | HLA class II | AIM | (Tarke et al., 2021) |
| RALTGIAVEQDKNTQ | S | 765 | 779 | HLA class II | ELISA | (Verhagen et al., 2021) |
| RDISTEIYQAGSTPCNGVEG | S | 466 | 485 | HLA class II | proliferation | (Low et al., 2021) |
| RFASVYAWNRKR | S | 346 | 357 | DR | proliferation | (Low et al., 2021) |
| RFASVYAWNRKRISN | S | 346 | 360 | DRB1*07:01/DRB1*14:01/DRB1*13:01 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020; Tarke et al., 2022) |
| RFASVYAWNRKRISNCVADY | S | 346 | 365 | HLA class II | proliferation | (Low et al., 2021) |
| RFNGIGVTQNVLYENQKLIA | S | 905 | 924 | DRB1*11:04/DRB1*15:01 | multimer staining | (Johansson et al., 2021) |
| REFVFKNIDGYFKIYSK | S | 190 | 206 | DRB3*02:02/DRB5*01:01 | ELISPOT | (Woldemeskel et al., 2021) |
| REGVFVSNGTHWFVT | S | 1091 | 1105 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| RISNCVADYSVLYNSASFS | S | 357 | 375 | HLA class II | ELISA | (Verhagen et al., 2021) |
| RKRISNCVAD | S | 355 | 364 | HLA class II | proliferation | (Low et al., 2021) |
| RKSNLKPFERDISTEIYQAG | S | 457 | 476 | DRB1*04:01/DRB3*01:01 | multimer staining | (Johansson et al., 2021) |
| RSFIEDLLFNKVT | S | 815 | 827 | DPA1*01:03/DPB1*04:01 | ELISPOT/ICS | (Woldemeskel et al., 2022) |
| RTQLPPAYTNSFTRG | S | 21 | 35 | HLA class II | AIM | (Tarke et al., 2022) |
| RVVVLSFELLHAPATVCGP | S | 509 | 527 | HLA class II | ELISA | (Verhagen et al., 2021) |
| SAIGKIQDSLSSTASALGKL | S | 929 | 948 | DRB1*04:01/DRB1*04:04 | multimer staining | (Johansson et al., 2021) |
| SALEPLVDLPIGINI | S | 221 | 235 | HLA class II | AIM | (Tarke et al., 2021) |
| SANNCTFEYVSQPFLMD | S | 162 | 178 | DPA1*01:03/DPB1*04:01 | ELISPOT | (Woldemeskel et al., 2021) |
| SASFSTFKCYGVSPT | S | 371 | 385 | DRB1*15:01 | AIM/ELISA/ICS | (Tarke et al., 2021; Zhang et al., 2022; Tarke et al., 2022; Li et al., 2021) |
| SCGSCCKFDEDDSEPVLKGV | S | 1249 | 1268 | DRB3*01:01 | multimer staining | (Johansson et al., 2021) |
| SETKCTLKSFTVEKGIYQTS | S | 297 | 316 | DRB1*04:01 | multimer staining | (Johansson et al., 2021) |
| SFIEDLLFNKVTLAD | S | 816 | 830 | DRB1*03:01/DRB1*12:01/DRB1*14:01/DQB1*05:03 | proliferation/AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020; Tarke et al., 2022; Low et al., 2021; Loyal et al., 2021) |
| SFTRGVYYPDKVFRS | S | 31 | 45 | HLA class II | AIM/ELISPOT | (Mateus et al., 2020; Tarke et al., 2022) |
| SFTVEKGIYQTSNFRVQPTE | S | 305 | 324 | DRB1*04:01/DRB1*07:01 | multimer staining | (Johansson et al., 2021) |
| SGWTAGAAAYYVGYL | S | 256 | 270 | HLA class II | AIM | (Tarke et al., 2022) |
| SIAIPTNFTISVTTE | S | 711 | 725 | HLA class II | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020; Tarke et al., 2022) |
| SIIAYTMSLGAENSV | S | 691 | 705 | HLA class II | AIM/ELISPOT | (Mateus et al., 2020; Tarke et al., 2022) |
| SKHTPINLVRDLPQG | S | 205 | 219 | HLA class II | ELISPOT | (Keller et al., 2020) |
| SKRSFIEDLLFNKVT | S | 813 | 827 | DRB1*07:01 | AIM | (Panikkar et al., 2022; Loyal et al., 2021) |
| SKRSFIEDLLFNKVTLA | S | 813 | 829 | DPA1*01:03/DPB1*04:01/DPA1*01:03/DPB1*04:01/DPA1*02:01/DPB1*01:01/DPA1*02:02/DPB1*02:01 | AIM/ELISPOT | (Woldemeskel et al., 2021; Dykema et al., 2021) |
| SKRSFIEDLLFNKVTLADA | S | 813 | 831 | HLA class II | ELISA | (Verhagen et al., 2021) |
| SLIDLQELGK | S | 1196 | 1205 | HLA class II | ICS | (Jin et al., 2021) |
| SLLIVNNATNVVIKV | S | 116 | 130 | DRB1*14:01/DRB1*12:01 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| SLSSTASALGKLQDVVNQNA | S | 937 | 956 | DRB1*04:01 | multimer staining | (Johansson et al., 2021) |
| SNFRVQPTESIVRFP | S | 316 | 330 | DRB1*07:01 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020; Tarke et al., 2022) |
| SNFRVQPTESIVRFPNITNL | S | 316 | 335 | HLA class II | proliferation | (Low et al., 2021) |
| SNGTHWFVTQRNFYEPQIIT | S | 1097 | 1116 | DRB1*04:01 | multimer staining | (Johansson et al., 2021) |
| SNLLLQYGSFCTQLNRA | S | 750 | 766 | DRB1*15:01 | ELISPOT | (Woldemeskel et al., 2021) |
| SPRRARSVASQSIIAYT | S | 680 | 696 | DQA1*01:03/DQB1*06:03 | ELISPOT | (Woldemeskel et al., 2021) |
| SQSIIAYTMSLGAENSVAYS | S | 689 | 708 | DRB1*04:01/DRB1*04:04/DRB1*07:01/DRB1*15:01 | multimer staining | (Johansson et al., 2021) |
| SSANNCTFEYVSQPF | S | 161 | 175 | HLA class II | AIM | (Tarke et al., 2021) |
| SSANNCTFEYVSQPFLM | S | 161 | 177 | HLA class II | AIM | (Pogorelyy et al., 2022) |
| SSANNCTFEYVSQPFLMDL | S | 161 | 179 | HLA class II | ELISA | (Verhagen et al., 2021) |
| SSANNCTFEYVSQPFLMDLE | S | 161 | 180 | DPB1*04:01 | multimer staining | (Johansson et al., 2021) |
| STECSNLLLQYGSFC | S | 746 | 760 | DQB1*06:02 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020; Tarke et al., 2022) |
| STECSNLLLQYGSFCTQ | S | 746 | 762 | DRB1*15:01 | AIM | (Pogorelyy et al., 2022) |
| STEIYQAGSTPCNGV | S | 469 | 483 | HLA class II | ELISA | (Verhagen et al., 2021) |
| SVASQSIIAYTMSLG | S | 686 | 700 | HLA class II | AIM | (Tarke et al., 2022) |
| SVLHSTQDLFLPFFS | S | 46 | 60 | DRB1*07:01/DQB1*02:02 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020; Tarke et al., 2022) |
| SVLYNSASFSTFKCY | S | 366 | 380 | DRB1*15:01 | AIM | (Tarke et al., 2021; Tarke et al., 2022) |
| SVLYNSASFSTFKCYGVSPT | S | 366 | 385 | HLA class II | proliferation | (Low et al., 2021) |
| SVTTEILPVSMTKTS | S | 721 | 735 | HLA class II | AIM | (Tarke et al., 2021) |
| SYQTQTNSPRRARSVASQSI | S | 673 | 692 | DRB1*07:01 | multimer staining | (Johansson et al., 2021) |
| TAPAICHDGKAHFPR | S | 1077 | 1091 | HLA class II | ELISA | (Verhagen et al., 2021) |
| TDEMIAQYTSALLAG | S | 875 | 889 | DRB1*04:04/DRB1*15:01/DQB1*06:02 | ELISPOT/AIM/ELISA | (Tarke et al., 2021; Titov et al., 2022; Peng et al., 2020; Mateus et al., 2020; Tarke et al., 2022) |
| TDNTFVSGNCDVVIG | S | 1117 | 1131 | HLA class II | ELISA | (Verhagen et al., 2021) |
| TECSNLLLQYGSFCTQL | S | 747 | 763 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| TESNKKFLPFQQFGRDIADT | S | 553 | 572 | DRB5*01:01 | multimer staining | (Johansson et al., 2021) |
| TFKCYGVSPTKLNDL | S | 376 | 390 | HLA class II | AIM/ICS | (Tarke et al., 2021; Mahajan et al., 2021) |
| TFKCYGVSPTKLNDLCFTNV | S | 376 | 395 | HLA class II | proliferation | (Low et al., 2021) |
| TITSGWTFGAGAALQ | S | 881 | 895 | DQB1*06:02/DQB1*04:02 | AIM | (Tarke et al., 2021; Tarke et al., 2022) |
| TKLNDLCFTNVYADS | S | 385 | 399 | HLA class II | ELISA | (Verhagen et al., 2021) |
| TLEILDITPCSFGGV | S | 581 | 595 | HLA class II | AIM/ELISA | (Tarke et al., 2021; Verhagen et al., 2021) |
| TLVKQLSSNFGAISS | S | 961 | 975 | DRB1*04:04 | AIM/ELISPOT | (Panikkar et al., 2022; Mateus et al., 2020) |
| TLVKQLSSNFGAISSVLNDI | S | 961 | 980 | DRB1*01:01/DRB1*04:04 | multimer staining/AIM | (Johansson et al., 2021) |
| TNVYADSFVIRGDEVRQIAP | S | 393 | 412 | DRB1*03:01/DRB3*01:01 | multimer staining | (Johansson et al., 2021) |
| TPPIKDFGGFNFSQI | S | 791 | 805 | DRB1*15:01 | AIM | (Tarke et al., 2021) |
| TQLNRALTGIAVEQD | S | 761 | 775 | DQB1*06:02/DQB1*04:02 | AIM/ELISPOT/ICS | (Tarke et al., 2021; Mateus et al., 2020; Zhang et al., 2022; Tarke et al., 2022) |
| TQLNRALTGIAVEQDKNTQ | S | 761 | 779 | HLA class II | ELISA | (Verhagen et al., 2021) |
| TQQLIRAAEIRASANLAATK | S | 1009 | 1028 | DRB1*03:01/DRB1*04:01 | multimer staining | (Johansson et al., 2021) |
| TQRNFYEPQIITTDNTFVSG | S | 1105 | 1124 | DRB1*03:01/DRB1*04:01 | multimer staining | (Johansson et al., 2021) |
| TRFASVYAWNRKRIS | S | 345 | 359 | HLA class II | ELISA | (Verhagen et al., 2021) |
| TRFASVYAWNRKRISNCVA | S | 345 | 363 | HLA class II | ELISA | (Verhagen et al., 2021) |
| TRFASVYAWNRKRISNCVAD | S | 345 | 364 | DRB1*03:01/DRB1*11:01/DRB5*01:01 | multimer staining | (Johansson et al., 2021) |
| TRFQTLLALHRSYLT | S | 236 | 250 | DRB1*01:01/DRB1*04:01/DRB1*15:01/DRB1*12:01/DRB1*14:01/DQB1*05:03 | multimer staining/AIM/ELISPOT | (Poluektov et al., 2021; Tarke et al., 2021; Mateus et al., 2020) |
| TRGVYYPDKVFRSSV | S | 33 | 47 | HLA class II | ELISA | (Verhagen et al., 2021) |
| TRGVYYPDKVFRSSVLHSTQ | S | 33 | 52 | DRB1*04:01/DRB3*01:01 | multimer staining | (Johansson et al., 2021) |
| TVYDPLQPELDSFKE | S | 1136 | 1150 | HLA class II | AIM | (Tarke et al., 2022) |
| VLLPLVSSQCVNLTT | S | 6 | 20 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| VLYQDVNCTEVPVAIHA | S | 610 | 626 | DRB1*13:01 | ELISPOT | (Woldemeskel et al., 2021) |
| VFAQVKQIYKTPPIK | S | 781 | 795 | DRB1*15:01 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020; Tarke et al., 2022) |
| VFKNIDGYFKIYSKHTPINL | S | 193 | 212 | DRB5*01:01 | multimer staining | (Johansson et al., 2021) |
| VFNATRFASVYAWNR | S | 341 | 355 | HLA class II | ICS/AIM/ELISPOT | (Mateus et al., 2020; Mahajan et al., 2021) |
| VGGNYNYLYRLFRKS | S | 445 | 459 | HLA class II | ELISA | (Verhagen et al., 2021) |
| VGGNYNYLYRLFRKSNLKP | S | 445 | 463 | HLA class II | ELISA/CBA | (Verhagen et al., 2021) |
| VGYQPYRVVVLSFELLHAPA | S | 503 | 522 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| VIAWNSNNLDSKVGGNYNYL | S | 433 | 452 | DRB1*15:01 | multimer staining | (Johansson et al., 2021) |
| VIRGDEVRQIAPGQT | S | 401 | 415 | DRB1*13:01 | AIM | (Tarke et al., 2021) |
| VIRGDEVRQIAPGQTGKIAD | S | 401 | 420 | DRB3*01:01 | multimer staining | (Johansson et al., 2021) |
| VNLTTRTQLPPAYTN | S | 16 | 30 | HLA class II | AIM | (Tarke et al., 2021) |
| VNNATNVVIKVCEFQFC | S | 120 | 136 | DRB3*02:02 | ELISPOT | (Woldemeskel et al., 2021) |
| VNNSYECDIPIGAGI | S | 656 | 670 | HLA class II | AIM | (Tarke et al., 2021) |
| VNNTVYDPLQPELDS | S | 1133 | 1147 | HLA class II | AIM | (Loyal et al., 2021) |
| VQIDRLITGRLQSLQ | S | 991 | 1005 | HLA class II | AIM/ELISPOT | (Mateus et al., 2020; Tarke et al., 2022) |
| VSMTKTSVDCTMYICGD | S | 729 | 745 | DQA1*02:01/DQB1*02:02//DQB1*03:03 | ELISPOT | (Woldemeskel et al., 2021) |
| VSQPFLMDLEGKQGN | S | 171 | 185 | DRB1*03:01 | AIM | (Tarke et al., 2021) |
| VSSQCVNLTTRTQLP | S | 11 | 25 | HLA class II | AIM | (Tarke et al., 2021) |
| VTLADAGFIKQYGDC | S | 826 | 840 | HLA class II | AIM | (Tarke et al., 2021) |
| VTQNVLYENQKLIAN | S | 911 | 925 | DRB1*12:01/DRB1*03:01 | AIM | (Tarke et al., 2021) |
| VVIKVCEFQFCNDPF | S | 126 | 140 | HLA class II | AIM/ELISPOT | (Tarke et al., 2021; Tarke et al., 2022)34 |
| VVLSFELLHAPATVC | S | 511 | 525 | DRB1*12:01/DRB1*14:01/DQB1*05:03 | ELISPOT/AIM | (Tarke et al., 2021; Peng et al., 2020) |
| VVNQNAQALNTLVKQ | S | 951 | 965 | HLA class II | AIM | (Tarke et al., 2022) |
| VYAWNRKRIS | S | 350 | 359 | DR | proliferation | (Low et al., 2021) |
| VYYPDKVFRSSVLHS | S | 36 | 50 | DRB1*13:01/DRB1*14:01/DRB1*03:01 | AIM | (Tarke et al., 2021) |
| VYYPDKVFRSSVLHSTQ | S | 36 | 52 | DPA1*01:03/DPB1*04:01 | ELISPOT | (Woldemeskel et al., 2021) |
| TNFTISVTTEILPVS | S | 716 | 730 | DQB1*06:03/DRB1*07:01/DRB1*14:01/DQB1*02:02 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020; Tarke et al., 2022) |
| TTAPAICHDGKAHFP | S | 1076 | 1090 | HLA class II | AIM/ELISPOT | (Mateus et al., 2020; Tarke et al., 2022) |
| TTDNTFVSGNCDVVI | S | 1116 | 1130 | HLA class II | AIM | (Tarke et al., 2022) |
| WNRKRISNCVADYSV | S | 353 | 367 | HLA class II | ELISA | (Verhagen et al., 2021) |
| WNRKRISNCVADYSVLYNS | S | 353 | 371 | HLA class II | ELISA/CBA | (Verhagen et al., 2021) |
| WNRKRISNCVADYSVLYNSA | S | 353 | 372 | DRB1*03:01/DRB4*01:01 | multimer staining | (Johansson et al., 2021) |
| WNSNNLDSKVGGNYN | S | 436 | 450 | HLA class II | AIM | (Tarke et al., 2021) |
| WNSNNLDSKVGGNYNYLYRL | S | 436 | 455 | HLA class II | proliferation | (Low et al., 2021) |
| WRVYSTGSNVFQTRAGCLIG | S | 633 | 652 | DRB1*07:01 | multimer staining | (Johansson et al., 2021) |
| WTFGAGAALQIPFAM | S | 886 | 900 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| YADSFVIRGDEVRQI | S | 396 | 410 | DRB1*13:01/DQB1*02:02 | AIM | (Tarke et al., 2021; Tarke et al., 2022) |
| YADSFVIRGDEVRQIAPGQT | S | 396 | 415 | HLA class II | proliferation | (Low et al., 2021) |
| YAWNRKRISNCVADY | S | 360 | 374 | DRB1*13:01 | ELISPOT/AIM | (Tarke et al., 2021; Peng et al., 2020; Tarke et al., 2022) |
| YAWNRKRISNCVADYSV | S | 351 | 367 | DRB3*02:02/DRB4*01:03 | ELISPOT | (Woldemeskel et al., 2021) |
| YENQKLIANQFNSAI | S | 917 | 931 | HLA class II | ELISA | (Verhagen et al., 2021) |
| YENQKLIANQFNSAIGKIQ | S | 917 | 935 | HLA class II | ELISA | (Verhagen et al., 2021) |
| YEQYIKWPWYIWLGF | S | 1206 | 1220 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| YFPLQSYGFQPTNGVGYQPY | S | 489 | 508 | DRB5*01:01 | multimer staining | (Johansson et al., 2021) |
| YGSFCTQLNRALTGI | S | 756 | 770 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| YLYRLFRKSNLKPFE | S | 451 | 465 | HLA class II | ICS/AIM | (Mahajan et al., 2021) |
| YNYLYRLFRKSNLKP | S | 449 | 463 | DPA1*01:03/DPB1*02:01 | ELISA/ELISPOT | (Keller et al., 2020; Verhagen et al., 2021) |
| YNYLYRLFRKSNLKPFERDI | S | 449 | 468 | DRB1*11:01/DRB1*11:04/DRB3*01:01 | multimer staining | (Johansson et al., 2021) |
| YQPYRVVVLSFELLHAPATV | S | 505 | 524 | DRB1*01:01 | multimer staining | (Johansson et al., 2021) |
| YQTSNFRVQPTESIVRFPN | S | 313 | 331 | HLA class II | ELISA | (Verhagen et al., 2021) |
| YQTSNFRVQPTESIVRFPNI | S | 313 | 332 | DRB1*04:01/DRB1*01:01 | multimer staining | (Johansson et al., 2021) |
| YVGYLQPRTFLLKYN | S | 266 | 280 | HLA class II | ICS/AIM | (Tarke et al., 2022) |
| ACFVLAAVYRINWITGGIA | M | 63 | 81 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| AIAMACLVGLMWLSY | M | 81 | 95 | HLA class II | AIM | (Tarke et al., 2021) |
| ASFRLFARTRSMWSFN | M | 98 | 113 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| ATSRTLSYYKLGASQ | M | 171 | 185 | DQB1*05:03/DRB1*16:01/DQB1*05:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| AVYRINWITGGIAIA | M | 69 | 83 | DRB1*01:02 | AIM | (Panikkar et al., 2022) |
| CLVGLMWLSYFIASF | M | 86 | 100 | DQB1*05:01/DRB1*12:02/DRB1*12:01/DQB1*05:03 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| EELKKLLEQWNLVIG | M | 11 | 25 | DQB1*05:02/DQB1*05:01 | ICS,AIM | (Tarke et al., 2021; Heide et al., 2021) |
| FIASFRLFARTRSMW | M | 96 | 110 | DRB1*03:01/DRB1*14:01/DQB1*05:03 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| FLFLTWICLLQFAYA | M | 26 | 40 | DQB1*05:03/DRB1*01:02/DQB1*05:01 | AIM | (Tarke et al., 2021) |
| FLWLLWPVTLACFVLA | M | 53 | 68 | HLA class II | AIM | (Hu et al., 2021) |
| FVLAAVYRINWITGGIAIAM | M | 65 | 84 | DRB1*01:01 | multimer staining | (Johansson et al., 2021) |
| GAVILRGHLRIAGHH | M | 141 | 155 | DRB1*15:01/DRB1*13:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| GAVILRGHLRIAGHHLG | M | 141 | 157 | DRB1*11:01 | AIM | (Pogorelyy et al., 2022) |
| GAVILRGHLRIAGHHLGR | M | 141 | 158 | DRB1*11:01/DRB1*13:01/DRB1*11:04 | ELISPOT/ELISA | (Titov et al., 2022; Peng et al., 2020) |
| GHHLGRCDIKDLPKEITVAT | M | 153 | 172 | DRB1*11:01/DRB1*11:04 | multimer staining | (Johansson et al., 2021) |
| GLMWLSYFIASFRLFARTRS | M | 89 | 108 | DRB1*01:01/DRB1*11:01 | multimer staining | (Johansson et al., 2021) |
| GTILTRPLLESELVI | M | 126 | 140 | DRB1*13:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| GTITVEELKKLLEQW | M | 6 | 20 | HLA class II | ICS | (Heide et al., 2021) |
| HLRIAGHHLGR | M | 148 | 158 | DRB1*11:01 | ICS/multimer staining/AIM | (Heide et al., 2021) |
| IAGHHLGRCDIKDLP | M | 151 | 165 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| IASFRLFARTRSMWSFNPET | M | 97 | 116 | DRB1*04:01/DRB1*07:01/DRB1*11:01 | multimer staining | (Johansson et al., 2021) |
| IGNYKLNTDHSSSSD | M | 201 | 215 | DRB1*03:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| IGNYKLNTDHSSSSDNIALL | M | 201 | 220 | DRB1*04:01 | multimer staining | (Johansson et al., 2021) |
| IKDLPKEITVATSRT | M | 161 | 175 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| IKDLPKEITVATSRTLSYYK | M | 161 | 180 | DRB1*03:01/DRB1*15:01 | multimer staining | (Johansson et al., 2021) |
| ITGGIAIAMACLVGL | M | 76 | 90 | DQB1*03:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| KEITVATSRTLSYYK | M | 166 | 180 | DPB1*02:01/DPA1*01:03/DPB1*04:01/DQA1*05:01/DQB1*02:01/DQA1*05:01/DQB1*03:01/DQA1*03:01/DQB1*03:02/DQA1*01:02/DQB1*06:02/DRB1*01:01/DRB1*03:01/DRB1*04:01/DRB1*04:05/DRB1*07:01/DRB1*08:02/DRB1*09:01/DRB1*11:01/DRB1*12:01/DRB1*13:02/DRB1*15:01/DRB3*01:01/DRB3*02:02/DRB4*01:01/DRB5*01:01/DQB1*06:03/DRB1*16:02/DRB1*15:01/DRB1*14:06/DRB1*14:01/DRB1*07:01/DRB1*03:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| LGASQRVAGDSGFAA | M | 181 | 195 | HLA class II | ICS/AIM/ELISPOT | (Tarke et al., 2021; Keller et al., 2020; Heide et al., 2021) |
| LGRCDIKDLPKEITV | M | 156 | 170 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| LIFLWLLWPVTLACF | M | 51 | 65 | DQB1*05:03/DRB1*01:02/DQB1*05:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| LLEQWNLVIGFLFLT | M | 16 | 30 | DQB1*05:03/DQB1*02:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| LLWPVTLACFVLAAV | M | 56 | 70 | DQB1*05:03/DQB1*06:03/DQB1*05:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| LNTDHSSSSDNIALL | M | 206 | 220 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| LRGHLRIAGHHLGRC | M | 145 | 159 | DRB1*11:01/DRB1*11:04/DRB1*08:01 | ELISPOT/AIM | (Panikkar et al., 2022; Keller et al., 2020) |
| LRGHLRIAGHHLGRCDIKDL | M | 145 | 164 | DRB1*03:01/DRB1*11:01/DRB1*11:04/DRB4*01:01 | multimer staining | (Johansson et al., 2021) |
| LRIAGHHLGRCDIKD | M | 149 | 163 | HLA class II | ELISPOT | (Keller et al., 2020) |
| LSYYKLGASQRVAGD | M | 176 | 190 | DRB1*01:01/DRB1*04:01/DRB1*15:01/DPB1*02:01/DQA1*05:01/DQB1*02:01/DQA1*05:01/DQB1*03:01/DQA1*01:01/DQB1*05:01/DQA1*01:02/DQB1*06:02/DRB1*03:01/DRB1*04:01/DRB1*04:05/DRB1*08:02/DRB1*09:01/DRB1*11:01/DRB1*12:01/DRB1*13:02/DRB3*01:01/DRB3*02:02/DRB4*01:01/DRB5*01:01/DQB1*03:01/DRB1*16:02/DRB1*16:01/DRB1*15:01/DRB1*14:06/DRB1*07:01/DRB1*01:01/DQB1*06:03/DQB1*06:02/DRB1*01:01/DRB3*02:02/DQB1*03:01/DQB1*02:01 | multimer staining /ICS/AIM/ELISPOT/ELISA | (Poluektov et al., 2021; Tarke et al., 2021; Titov et al., 2022; Nelde et al., 2021; Prakash et al., 2021; Heide et al., 2021) |
| LYIIKLIFLWLLWPV | M | 46 | 60 | DRB1*12:01/DQB1*02:01 | AIM | (Tarke et al., 2021) |
| MADSNGTITVEELKK | M | 1 | 15 | HLA class II | ICS | (Heide et al., 2021) |
| NLVIGFLFLTWICLL | M | 21 | 35 | DRB1*01:02/DQB1*05:01 | AIM | (Tarke et al., 2021) |
| NRFLYIIKLIFLWLLWPVTL | M | 43 | 62 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| NRNRFLYIIKLIFLW | M | 41 | 55 | DQB1*05:03/DRB1*03:01/DRB1*12:01/DQB1*02:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| NVPLHGTILTRPLLE | M | 121 | 135 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| QFAYANRNRFLYIIK | M | 36 | 50 | DRB1*14:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| QFAYANRNRFLYIIKLI | M | 36 | 52 | DRB1*11:01 | multimer staining | (Johansson et al., 2021) |
| MWLSYFIASFRLFAR | M | 91 | 105 | DQB1*02:01/DRB1*16:02/DRB1*16:01/DRB1*14:06/DRB1*14:01/DRB1*03:01/DQB1*05:03/DQB1*05:02/DQB1*05:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| RGHLRIAGHHLGRCD | M | 146 | 160 | DPB1*02:01/DPA1*01:03/DPB1*04:01/DQA1*05:01/DQB1*03:01/DQA1*01:01/DQB1*05:01/DRB1*01:01/DRB1*03:01/DRB1*04:01/DRB1*04:05/DRB1*08:02/DRB1*09:01/DRB1*12:01/DRB1*13:02/DRB3*01:01/DRB3*02:02/DRB4*01:01/DRB5*01:01/DRB1*07:01/DRB1*15:01/DRB1*14:01/DRB1*13:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021; Le Bert et al., 2021) |
| RGHLRIAGHHLGRCDIK | M | 146 | 162 | DRB1*11:01 | AIM | (Pogorelyy et al., 2022) |
| RLFARTRSMWSFNPE | M | 101 | 115 | DRB1*14:01/DQB1*05:03 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| RPLLESELVIGAVIL | M | 131 | 145 | DQB1*02:02 | AIM | (Tarke et al., 2021) |
| RTRSMWSFNPETNILLNVPL | M | 105 | 124 | DRB1*01:01/DRB1*04:01 | multimer staining | (Johansson et al., 2021) |
| RVAGDSGFAAYSRYR | M | 186 | 200 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| SELVIGAVILRGHLR | M | 136 | 150 | DQB1*06:02/DRB1*16:01/DRB1*15:01/DRB1*14:01/DRB1*13:01/DRB1*01:02/DQB1*06:03 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| SFNPETNILLNVPLH | M | 111 | 125 | DRB1*01:02 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| SGFAAYSRYRIGNYK | M | 191 | 205 | DRB1*15:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| SRTLSYYKLGASQRV | M | 173 | 187 | DRB5*01:02/DRB5*01:01 | ELISPOT | (Keller et al., 2020) |
| SYFIASFRLF | M | 94 | 103 | HLA class II | ICS | (Jin et al., 2021) |
| SYYKLGASQRVAGDS | M | 177 | 191 | DRB1*07:01/DQA1*05:01/DQB1*03:01/DRB1*01:01 | ELISPOT | (Keller et al., 2020) |
| SYYKLGASQRVAGDSGFAAY | M | 177 | 196 | DRB1*04:01/DRB1*07:01/DRB1*11:01/DRB5*01:01 | multimer staining | (Johansson et al., 2021) |
| TNILLNVPLHGTILT | M | 116 | 130 | DRB1*10:01/DRB1*16:02/DRB1*15:01/DRB1*14:06/DRB1*14:01/DRB1*12:02 | AIM | (Tarke et al., 2021) |
| TRSMWSFNPETNILL | M | 106 | 120 | DQB1*05:02/DQB1*05:03/DRB1*01:02/DQB1*05:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| TNILLNVPLHGTILTRP | M | 116 | 132 | DRB3*02:02 | AIM | (Pogorelyy et al., 2022) |
| TSRTLSYYKLGASQRVA | M | 172 | 188 | DRB1*07:01/DRB1*01:01 | ELISPOT/ELISA/ICS | (Titov et al., 2022; Peng et al., 2020) |
| TVATSRTLSYYKLGASQRVA | M | 169 | 188 | DRB1*03:01/DRB1*04:01/DRB1*07:01/DRB1*11:01/DRB5*01:01/DRB1*04:01/DRB1*04:01 | multimer staining | (Johansson et al., 2021) |
| TVEELKKLLEQWNLVIGFLF | M | 9 | 28 | DRB1*07:01 | multimer staining | (Johansson et al., 2021) |
| VLAAVYRINWITGGI | M | 66 | 80 | DQB1*05:01/DRB1*14:01/DRB1*12:02/DQB1*05:03 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| WICLLQFAYANRNRF | M | 31 | 45 | DRB1*03:01/DRB1*14:01/DQB1*05:03 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| YRINWITGGIAIAMA | M | 71 | 85 | DQB1*02:02/DRB1*16:01/DRB1*15:01/DRB1*14:01/DRB1*13:01/DRB1*12:01/DRB1*10:01/DRB1*07:01/DQB1*06:03/DQB1*06:02/DQB1*05:03/DQB1*05:02/DQB1*05:01/DQB1*03:01 | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| YSRYRIGNYK | M | 196 | 205 | HLA class II | proliferation | (Jin et al., 2021) |
| YSRYRIGNYKLNTDH | M | 196 | 210 | HLA class II | ICS/AIM | (Tarke et al., 2021; Heide et al., 2021) |
| YYKLGASQRVA | M | 178 | 188 | DRB1*01:01 | ICS | (Heide et al., 2021) |
| ALLAVFQSASKIITL | ORF3a | 51 | 65 | DRB1*11:01/DQB1*03:01 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| CNLLLLFVTVYSHLL | ORF3a | 81 | 95 | DRB1*07:01/DRB1*11:01/DQB1*02:01 | AIM | (Tarke et al., 2021) |
| EHVTFFIYNKIVDEP | ORF3a | 226 | 240 | DQB1*05:01/DRB1*08:01/DRB1*11:01/DQB1*02:01 | AIM | (Tarke et al., 2021) |
| FIYNKIVDEPEEHVQ | ORF3a | 231 | 245 | DRB1*08:01/DQB1*05:01 | AIM | (Tarke et al., 2021) |
| FLCWHTNCYDYCIPY | ORF3a | 146 | 160 | DQB1*05:03 | AIM | (Tarke et al., 2021) |
| FMRIFTIGTVTLKQG | ORF3a | 4 | 18 | DR | ELISPOT/ICS | (Nelde et al., 2021) |
| GSSGVVNPVMEPIYD | ORF3a | 251 | 265 | DQB1*04:02 | AIM | (Tarke et al., 2021) |
| INFVRIIMRLWLCWKCRSKN | ORF3a | 118 | 137 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| KIITLKKRWQLALSK | ORF3a | 61 | 75 | DRB1*11:01 | AIM | (Tarke et al., 2021) |
| KKRWQLALSKGVHFV | ORF3a | 66 | 80 | DRB1*07:01 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| KNPLLYDANYFLCWH | ORF3a | 136 | 150 | DRB1*15:01/DQB1*05:03 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| LEAPFLYLYALVYFL | ORF3a | 101 | 115 | DRB1*11:01/DQB1*02:01 | AIM | (Tarke et al., 2021) |
| LVAAGLEAPFLYLYA | ORF3a | 96 | 110 | DQB1*02:02/DQB1*02:01 | AIM | (Tarke et al., 2021) |
| LVYFLQSINFVRIIM | ORF3a | 111 | 125 | DRB1*12:01/DRB1*14:01/DQB1*05:03 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| LYLYALVYFLQSINF | ORF3a | 106 | 120 | DQB1*02:01/DRB1*12:01/DRB1*11:01/DQB1*05:03/DQB1*03:02 | AIM | (Tarke et al., 2021) |
| RLWLCWKCRSKNPLL | ORF3a | 126 | 140 | HLA class II | AIM | (Tarke et al., 2021) |
| SDFVRATATIPIQAS | ORF3a | 26 | 40 | HLA class II | ELISPOT | (Mateus et al., 2020; de Castro et al., 2022) |
| TDTGVEHVTFFIYNK | ORF3a | 221 | 235 | HLA class II | AIM | (Tarke et al., 2021) |
| TNCYDYCIPYNSVTS | ORF3a | 151 | 165 | DQB1*05:01 | AIM | (Tarke et al., 2021) |
| QSINFVRIIMRLWLC | ORF3a | 116 | 130 | DQB1*06:02/DRB1*15:01/DRB1*14:01/DRB1*12:01/DRB1*11:01/DRB1*03:01 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| VRIIMRLWLCWKCRS | ORF3a | 121 | 135 | DRB1*11:01 | AIM | (Tarke et al., 2021) |
| YFTSDYYQLYSTQLS | ORF3a | 206 | 220 | DRB1*16:02 | AIM | (Tarke et al., 2021) |
| YDANYFLCWHTNCYD | ORF3a | 141 | 155 | HLA class II | AIM | (Tarke et al., 2021) |
| AEILLIIMRTFKVSI | ORF6 | 12 | 26 | DRB1 | ELISPOT | (Prakash et al., 2021) |
| IAEILLIIMRTFKVS | ORF6 | 11 | 25 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| IWNLDYIINLIIKNL | ORF6 | 26 | 40 | DR | ELISPOT/ICS | (Nelde et al., 2021; Mateus et al., 2020) |
| LIIMRTFKVSIWNLD | ORF6 | 16 | 30 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| MFHLVDFQVTIAEIL | ORF6 | 1 | 15 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| TFKVSIWNLDYIINL | ORF6 | 21 | 35 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| YIINLIIKNLSKSLT | ORF6 | 31 | 45 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| AAIVFITLCFTLKRKT | ORF7a | 105 | 120 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| DGVKHVYQLRARSVSPKL | ORF7a | 4 | 21 | HLA class II | ELISPOT | (Peng et al., 2020) |
| QEEVQELYSPIFLIV | ORF7a | 90 | 104 | DR | ELISPOT | (Nelde et al., 2021) |
| IILFLALITLATCEL | ORF7a | 3 | 17 | DRB1 | ELISPOT | (Prakash et al., 2021) |
| LYSPIFLIVAAIVFI | ORF7a | 96 | 110 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| MKIILFLALITLATC | ORF7a | 1 | 15 | DRB1 | ELISPOT | (Prakash et al., 2021; Mateus et al., 2020) |
| SPIFLIVAAIVFITL | ORF7a | 98 | 112 | DRB1 | ELISPOT | (Prakash et al., 2021) |
| VKHVYQLRARSVSPK | ORF7a | 71 | 85 | HLA class II | ELISPOT | (Mateus et al., 2020) |
| DFYLCFLAFLLFLVL | ORF7b | 8 | 22 | DRB1 | ELISPOT | (Prakash et al., 2021) |
| ARKSAPLIELCVDEA | ORF8 | 51 | 65 | HLA class II | AIM | (Tarke et al., 2021) |
| CVDEAGSKSPIQYID | ORF8 | 61 | 75 | HLA class II | AIM | (Tarke et al., 2021) |
| DFLEYHDVRVVLDFI | ORF8 | 107 | 121 | DQB1*06:04/DRB1*15:02/DQB1*05:02 | AIM | (Tarke et al., 2021) |
| EDFLEYHDVRVVLDF | ORF8 | 106 | 120 | DQB1*06:04/DRB1*13:02/DRB1*15:02/DQB1*05:02 | AIM | (Tarke et al., 2021) |
| FHQECSLQSCTQHQP | ORF8 | 16 | 30 | HLA class II | AIM | (Tarke et al., 2021) |
| FLGIITTVAAFHQEC | ORF8 | 6 | 20 | HLA class II | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| FTINCQEPKLGSLVV | ORF8 | 86 | 100 | HLA class II | AIM | (Tarke et al., 2021) |
| FYSKWYIRVGARKSA | ORF8 | 41 | 55 | DQB1*06:01/DRB1*14:01/DRB1*13:03/DRB1*11:04/DRB1*11:01/DRB1*07:01/DRB1*04:02/DRB1*14:06/DRB1*15:01/DRB1*15:02/DRB1*16:01/DRB1*16:02 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| GSLVVRCSFYEDFLE | ORF8 | 96 | 110 | DQB1*05:02/DQB1*05:03 | AIM | (Tarke et al., 2021) |
| IGNYTVSCLPFTINC | ORF8 | 76 | 90 | DQB1*03:03/DRB1*15:02 | AIM | (Tarke et al., 2021) |
| IQYIDIGNYTVSCLP | ORF8 | 71 | 85 | DRB1*13:02/DRB1*11:04 | AIM | (Tarke et al., 2021) |
| PCPIHFYSKWYIRVG | ORF8 | 36 | 50 | DRB1*08:02/DRB1*16:01/DRB1*15:02/DRB1*15:01/DRB1*13:01 | AIM | (Tarke et al., 2021) |
| PLIELCVDEAGSKSP | ORF8 | 56 | 70 | HLA class II | AIM | (Tarke et al., 2021) |
| QEPKLGSLVVRCSFY | ORF8 | 91 | 105 | DRB1*11:04 | AIM | (Tarke et al., 2021) |
| MKFLVFLGIITTVAA | ORF8 | 1 | 15 | DRB1 | ELISPOT | (Prakash et al., 2021) |
| MKFLVFLGIITTVAAFH | ORF8 | 1 | 17 | HLA class II | ELISPOT | (de Castro et al., 2022) |
| RCSFYEDFLEYHDVR | ORF8 | 101 | 115 | DQB1*05:02 | AIM | (Tarke et al., 2021) |
| SKWYIRVGARKSAPL | ORF8 | 43 | 57 | DR | ELISPOT/ICS | (Nelde et al., 2021; de Castro et al., 2022) |
| SLQSCTQHQPYVVDD | ORF8 | 21 | 35 | HLA class II | AIM | (Tarke et al., 2021) |
| TQHQPYVVDDPCPIH | ORF8 | 26 | 40 | DRB1*13:02 | AIM | (Tarke et al., 2021) |
| TTVAAFHQECSLQSC | ORF8 | 11 | 25 | DQB1*05:02 | AIM | (Tarke et al., 2021) |
| YIRVGARKSAPLIEL | ORF8 | 46 | 60 | DRB1*11:04/DRB1*13:02/DRB1*15:01/DRB1*16:01/DQB1*03:01 | AIM/ELISPOT | (Tarke et al., 2021; Mateus et al., 2020) |
| YVVDDPCPIHFYSKW | ORF8 | 31 | 45 | DRB1*13:02/DRB1*15:02 | AIM | (Tarke et al., 2021) |
| FAFPFTIYSL | ORF10 | 7 | 16 | HLA class II | ELISPOT | (Ma et al., 2021) |
| INVFAFPFTIYSLLL | ORF10 | 4 | 18 | DR | ELISPOT | (Nelde et al., 2021) |
Notes:
HTMA: high throughput multiplexed assay, is one method analyzing TCRs after sorting antigen-specific (CD3CD8CD137) T cells.
SPR: surface plasmon resonance, is one method detctcting the binding of MHC-peptide complex and the TCRs.
CBA: cytometric bead array.
Among all the studies collected here, 19 reported both CD8+ T-cell epitopes and CD4+ T-cell epitopes, 35 only reported CD8+ T-cell epitopes, and 16 only reported CD4+ T-cell epitopes. A total of 2214 SARS-CoV-2 antigen-specific T-cell epitopes were involved, including 1349 CD8+ T-cell epitopes and 790 CD4+ T-cell epitopes. Fig. 1A and 1B display the predominant HLA class I allotypes and HLA class II allotypes presenting these epitope peptides, respectively. Of these, 678 (50.2%) CD8+ T-cell epitopes are restricted by HLA-A0201, A2402, B0702, A0101, A1101, or B0801. The remainder are restricted mainly by 12 HLA-A, 8 HLA-B and 4 HLA-C supertypes. For the CD4+ T-cell epitopes, the majority of currently described restrictions apply to 10 DRB1 and 5 DQB1 supertypes. Obviously, these HLA allotypes cannot yet cover the major populations in an indicated geographic region. Further efforts are required to focus more on the regional dominant HLA supertypes for the design of regional vaccines and SARA-CoV-2-specific T-cell detection systems. In addition, 74.54% of all CD8+ T-cell epitopes were derived from the S protein and nonstructural proteins (Fig. 1C), while 80.91% of all CD4+ T-cell epitopes were derived from the S protein, N protein and nonstructural proteins (Fig. 1D).
Fig. 1.
HLA restriction and protein distribution of validated CD8+ T cell epitopes and CD4+ T cell epitopes in SARS-CoV-2 proteome. (A) and (B) displayed the number of CD8+ T-cell epitopes and CD4+ T-cell epitopes restricted by each HLA allotype, respectively. (C) and (D) showed the fraction of CD8+ T-cell epitopes and CD4+ T-cell epitopes in each SARS-CoV-2 protein, respectively.
6. Conclusion
This review systemically collected the CD8+ T-cell epitopes and CD4+ T-cell epitopes defined from the SARS-CoV-2 proteome during the last three years and displayed their HLA restrictions and the methods verifying their immunogenicity. These data will benefit the investigation of host cellular immunity and the development of vaccines and specific T-cell detection systems for SARS-CoV-2 infection.
Declaration of Competing Interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Acknowledgments
This work was supported by National Nature Science Foundation of China (82041006) and the foundation from State Key Laboratory of Pathogen and Biosecurity (SKLPBS2139).
Data Availability
The data that has been used is confidential.
References
- Yu P., Qi F., Xu Y., Li F., Liu P., Liu J., Bao L., Deng W., Gao H., Xiang Z., Xiao C., Lv Q., Gong S., Liu J., Song Z., Qu Y., Xue J., Wei Q., Liu M., Wang G., Wang S., Yu H., Liu X., Huang B., Wang W., Zhao L., Wang H., Ye F., Zhou W., Zhen W., Han J., Wu G., Jin Q., Wang J., Tan W., Qin C. Age-related rhesus macaque models of COVID-19. Anim. Models Exp. Med. 2020;3:93–97. doi: 10.1002/ame2.12108. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rydyznski Moderbacher C., Ramirez S.I., Dan J.M., Grifoni A., Hastie K.M., Weiskopf D., Belanger S., Abbott R.K., Kim C., Choi J., Kato Y., Crotty E.G., Kim C., Rawlings S.A., Mateus J., Tse L.P.V., Frazier A., Baric R., Peters B., Greenbaum J., Ollmann Saphire E., Smith D.M., Sette A., Crotty S. Antigen-specific adaptive immunity to SARS-CoV-2 in acute COVID-19 and associations with age and disease severity. Cell. 2020;183:996–1012. doi: 10.1016/j.cell.2020.09.038. e19. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Oberhardt V., Luxenburger H., Kemming J., Schulien I., Ciminski K., Giese S., Csernalabics B., Lang-Meli J., Janowska I., Staniek J., Wild K., Basho K., Marinescu M.S., Fuchs J., Topfstedt F., Janda A., Sogukpinar O., Hilger H., Stete K., Emmerich F., Bengsch B., Waller C.F., Rieg S., Sagar, Boettler T., Zoldan K., Kochs G., Schwemmle M., Rizzi M., Thimme R., Neumann-Haefelin C., Hofmann M. Rapid and stable mobilization of CD8+ T cells by SARS-CoV-2 mRNA vaccine. Nature. 2021;597:268–273. doi: 10.1038/s41586-021-03841-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zuo J., Dowell A.C., Pearce H., Verma K., Long H.M., Begum J., Aiano F., Amin-Chowdhury Z., Hoschler K., Brooks T., Taylor S., Hewson J., Hallis B., Stapley L., Borrow R., Linley E., Ahmad S., Parker B., Horsley A., Amirthalingam G., Brown K., Ramsay M.E., Ladhani S., Moss P. Robust SARS-CoV-2-specific T cell immunity is maintained at 6 months following primary infection. Nat. Immunol. 2021;22:620–626. doi: 10.1038/s41590-021-00902-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Toor S.M., Saleh R., Sasidharan Nair V., Taha R.Z., Elkord E. T-cell responses and therapies against SARS-CoV-2 infection. Immunology. 2021;162:30–43. doi: 10.1111/imm.13262. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Caccamo N., Sullivan L.C., Brooks A.G., Dieli F. Harnessing HLA-E-restricted CD8 T lymphocytes for adoptive cell therapy of patients with severe COVID-19. Br. J. Haematol. 2020;190:e185–e187. doi: 10.1111/bjh.16895. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nitschke K., Luxenburger H., Kiraithe M.M., Thimme R., Neumann-Haefelin C. CD8+ T-Cell responses in Hepatitis B and C: the HLA-A, B, and C of Hepatitis B and C. Dig. Dis. 2016;34:396–409. doi: 10.1159/000444555. [DOI] [PubMed] [Google Scholar]
- Roche P.A., Furuta K. The ins and outs of MHC class II-mediated antigen processing and presentation. Nat. Rev. Immunol. 2015;15:203–216. doi: 10.1038/nri3818. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Elahi S., Horton H. Association of HLA-alleles with the immune regulation of chronic viral infections. Int. J. Biochem. Cell Biol. 2012;44:1361–1365. doi: 10.1016/j.biocel.2012.05.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wang L., Zou Z.-Q., Wang K. Clinical relevance of HLA gene variants in HBV infection. J. Immunol. Res. 2016;2016 doi: 10.1155/2016/9069375. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Boeijen L.L., Hoogeveen R.C., Boonstra A., Lauer G.M. Hepatitis B virus infection and the immune response: The big questions. Best Pract. Res., Clin. Gastroenterol. 2017;31:265–272. doi: 10.1016/j.bpg.2017.05.003. [DOI] [PubMed] [Google Scholar]
- Medzhitov R. Recognition of microorganisms and activation of the immune response. Nature. 2007;449:819–826. doi: 10.1038/nature06246. [DOI] [PubMed] [Google Scholar]
- Littera R., Campagna M., Deidda S., Angioni G., Cipri S., Melis M., Firinu D., Santus S., Lai A., Porcella R., Lai S., Rassu S., Scioscia R., Meloni F., Schirru D., Cordeddu W., Kowalik M.A., Serra M., Ragatzu P., Carta M.G., Del Giacco S., Restivo A., Deidda S., Orrà S., Palimodde A., Perra R., Orrà G., Conti M., Balestrieri C., Serra G., Onali S., Marongiu F., Perra A., Chessa L. Human leukocyte antigen complex and other immunogenetic and clinical factors influence susceptibility or protection to SARS-CoV-2 infection and severity of the disease course. The sardinian experience. Front. Immunol. 2020;11 doi: 10.3389/fimmu.2020.605688. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Augusto, D. G.; Yusufali, T.; Peyser, N. D.; Butcher, X.; Marcus, G. M.; Olgin, J. E.; Pletcher, M. J.; Maiers, M.; Hollenbach, J. A. HLA-B*15:01 is associated with asymptomatic SARS-CoV-2 infection. medRxiv 2021, 2021.05.13.21257065.
- Wang F., Huang S., Gao R., Zhou Y., Lai C., Li Z., Xian W., Qian X., Li Z., Huang Y., Tang Q., Liu P., Chen R., Liu R., Li X., Tong X., Zhou X., Bai Y., Duan G., Zhang T., Xu X., Wang J., Yang H., Liu S., He Q., Jin X., Liu L. Initial whole-genome sequencing and analysis of the host genetic contribution to COVID-19 severity and susceptibility. Cell Discov. 2020;6:83. doi: 10.1038/s41421-020-00231-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Matern B.M., Olieslagers T.I., Voorter C.E.M., Groeneweg M., Tilanus M.G.J. Insights into the polymorphism in HLA-DRA and its evolutionary relationship with HLA haplotypes. HLA. 2020;95:117–127. doi: 10.1111/tan.13730. [DOI] [PubMed] [Google Scholar]
- Zidi I., Laaribi A.B., Bortolotti D., Belhadj M., Mehri A., Yahia H.B., Babay W., Chaouch H., Zidi N., Letaief A., Yacoub S., Boukadida J., Di Luca D., Hannachi N., Rizzo R. HLA-E polymorphism and soluble HLA-E plasma levels in chronic hepatitis B patients. HLA. 2016;87:153–159. doi: 10.1111/tan.12767. [DOI] [PubMed] [Google Scholar]
- Lan J., Ge J., Yu J., Shan S., Zhou H., Fan S., Zhang Q., Shi X., Wang Q., Zhang L., Wang X. Structure of the SARS-CoV-2 spike receptor-binding domain bound to the ACE2 receptor. Nature. 2020;581:215–220. doi: 10.1038/s41586-020-2180-5. [DOI] [PubMed] [Google Scholar]
- Naqvi A.A.T., Fatima K., Mohammad T., Fatima U., Singh I.K., Singh A., Atif S.M., Hariprasad G., Hasan G.M., Hassan M.I. Insights into SARS-CoV-2 genome, structure, evolution, pathogenesis and therapies: Structural genomics approach. Biochim. Biophys. Acta Mol. Basis Dis. 2020;1866 doi: 10.1016/j.bbadis.2020.165878. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tang T., Bidon M., Jaimes J.A., Whittaker G.R., Daniel S. Coronavirus membrane fusion mechanism offers a potential target for antiviral development. Antiviral Res. 2020;178 doi: 10.1016/j.antiviral.2020.104792. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Li S., Yuan L., Dai G., Chen R.A., Liu D.X., Fung T.S. Regulation of the ER stress response by the ion channel activity of the infectious bronchitis coronavirus envelope protein modulates virion release, apoptosis, viral fitness, and pathogenesis. Front. Microbiol. 2020;10 doi: 10.3389/fmicb.2019.03022. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cong Y., Ulasli M., Schepers H., Mauthe M., V’kovski P., Kriegenburg F., Thiel V., de Haan Cornelis A.M., Reggiori F., Dutch Rebecca E. Nucleocapsid protein recruitment to replication-transcription complexes plays a crucial role in coronaviral life cycle. J. Virol. 2020;94:e01925. doi: 10.1128/JVI.01925-19. -19. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zelba H., Worbs D., Harter J., Pieper N., Kyzirakos-Feger C., Kayser S., Seibold M., Bartsch O., KÃdding J., Biskup S. A highly specific assay for the detection of SARS-CoV-2-reactive CD4+ and CD8+ T cells in COVID-19 patients. J. Immunol. 2021;206:580. doi: 10.4049/jimmunol.2000811. [DOI] [PubMed] [Google Scholar]
- Grifoni A., Weiskopf D., Ramirez S.I., Mateus J., Dan J.M., Moderbacher C.R., Rawlings S.A., Sutherland A., Premkumar L., Jadi R.S., Marrama D., de Silva A.M., Frazier A., Carlin A.F., Greenbaum J.A., Peters B., Krammer F., Smith D.M., Crotty S., Sette A. Targets of T cell responses to SARS-CoV-2 coronavirus in humans with COVID-19 disease and unexposed individuals. Cell. 2020;181:1489–1501. doi: 10.1016/j.cell.2020.05.015. e15. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jiang S., Wu S., Zhao G., He Y., Guo X., Zhang Z., Hou J., Ding Y., Cheng A., Wang B. Identification of a promiscuous conserved CTL epitope within the SARS-CoV-2 spike protein. Emerg. Microbes Infect. 2022;11:730–740. doi: 10.1080/22221751.2022.2043727. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shafer-Weaver K., Sayers T., Strobl S., Derby E., Ulderich T., Baseler M., Malyguine A. The Granzyme B ELISPOT assay: an alternative to the 51Cr-release assay for monitoring cell-mediated cytotoxicity. J. Transl. Med. 2003;1:14. doi: 10.1186/1479-5876-1-14. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Freer G., Rindi L. Intracellular cytokine detection by fluorescence-activated flow cytometry: Basic principles and recent advances. Methods. 2013;61:30–38. doi: 10.1016/j.ymeth.2013.03.035. [DOI] [PubMed] [Google Scholar]
- Ji N., Forsthuber T.G. In: Multiple Sclerosis: Methods and Protocols. Weissert R., editor. Springer New York; New York, NY: 2016. ELISPOT Techniques; pp. 63–71. [Google Scholar]
- Portilho A.I., Gimenes Lima G., De Gaspari E. Enzyme-linked immunosorbent assay: an adaptable methodology to study SARS-CoV-2 humoral and cellular immune responses. J. Clin. Med. 2022;11 doi: 10.3390/jcm11061503. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Poluektov Y., George M., Daftarian P., Delcommenne M.C. Assessment of SARS-CoV-2 specific CD4+ and CD8+ T cell responses using MHC class I and II tetramers. Vaccine. 2021;39:2110–2116. doi: 10.1016/j.vaccine.2021.03.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Meyers L.M., GutiÃrrez A.H., Boyle C.M., Terry F., McGonnigal B.G., Salazar A., Princiotta M.F., Martin W.D., De Groot A.S., Moise L. Highly conserved, non-human-like, and cross-reactive SARS-CoV-2 T cell epitopes for COVID-19 vaccine design and validation. NPJ Vaccines. 2021;6:71. doi: 10.1038/s41541-021-00331-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhang H., Deng S., Ren L., Zheng P., Hu X., Jin T., Tan X. Profiling CD8+ T cell epitopes of COVID-19 convalescents reveals reduced cellular immune responses to SARS-CoV-2 variants. Cell Rep. 2021;36 doi: 10.1016/j.celrep.2021.109708. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Paul S., Croft N.P., Purcell A.W., Tscharke D.C., Sette A., Nielsen M., Peters B. Benchmarking predictions of MHC class I restricted T cell epitopes in a comprehensively studied model system. PLoS Comput. Biol. 2020;16 doi: 10.1371/journal.pcbi.1007757. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Saini S.K., Hersby D.S., Tamhane T., Povlsen H.R., Hernandez S.P.A., Nielsen M., Gang A.O., Hadrup S.R. SARS-CoV-2 genome-wide T cell epitope mapping reveals immunodominance and substantial CD8+ T cell activation in COVID-19 patients. Sci. Immunol. 2021;6:eabf7550. doi: 10.1126/sciimmunol.abf7550. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Snyder, T. M.; Gittelman, R. M.; Klinger, M.; May, D. H.; Osborne, E. J.; Taniguchi, R.; Zahid, H. J.; Kaplan, I. M.; Dines, J. N.; Noakes, M. T.; Pandya, R.; Chen, X.; Elasady, S.; Svejnoha, E.; Ebert, P.; Pesesky, M. W.; Almeida, P. D.; O’Donnell, H.; DeGottardi, Q.; Keitany, G.; Lu, J.; Vong, A.; Elyanow, R.; Fields, P.; Greissl, J.; Baldo, L.; Semprini, S.; Cerchione, C.; Nicolini, F.; Mazza, M.; Delmonte, O. M.; Dobbs, K.; Laguna-Goya, R.; CarreÃo-Tarragona, G.; Barrio, S.; Imberti, L.; Sottini, A.; Quiros-Roldan, E.; Rossi, C.; Biondi, A.; Bettini, L. R.; D’Angio, M.; Bonfanti, P.; Tompkins, M. F.; Alba, C.; Dalgard, C.; Sambri, V.; Martinelli, G.; Goldman, J. D.; Heath, J. R.; Su, H. C.; Notarangelo, L. D.; Paz-Artal, E.; Martinez-Lopez, J.; Carlson, J. M.; Robins, H. S. Magnitude and Dynamics of the T-Cell Response to SARS-CoV-2 Infection at Both Individual and Population Levels. medRxiv 2020, 2020.07.31.20165647.
- Tarke A., Sidney J., Kidd C.K., Dan J.M., Ramirez S.I., Yu E.D., Mateus J., da Silva Antunes R., Moore E., Rubiro P., Methot N., Phillips E., Mallal S., Frazier A., Rawlings S.A., Greenbaum J.A., Peters B., Smith D.M., Crotty S., Weiskopf D., Grifoni A., Sette A. Comprehensive analysis of T cell immunodominance and immunoprevalence of SARS-CoV-2 epitopes in COVID-19 cases. Cell Rep. Med. 2021;2 doi: 10.1016/j.xcrm.2021.100204. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lee Y.S., Hong S.H., Park H.J., Lee H.Y., Hwang J.Y., Kim S.Y., Park J.W., Choi K.S., Seong J.K., Park S.I., Lee S.M., Hwang K.A., Yun J.W., Nam J.H. Peptides derived from S and N proteins of severe acute respiratory syndrome coronavirus 2 induce T cell responses: a proof of concept for T cell vaccines. Front Microbiol. 2021;12 doi: 10.3389/fmicb.2021.732450. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Szeto C., Chatzileontiadou D.S.M., Nguyen A.T., Sloane H., Lobos C.A., Jayasinghe D., Halim H., Smith C., Riboldi-Tunnicliffe A., Grant E.J., Gras S. The presentation of SARS-CoV-2 peptides by the common HLA-A∗02:01 molecule. iScience. 2021;24 doi: 10.1016/j.isci.2021.102096. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weingarten-Gabbay S., Klaeger S., Sarkizova S., Pearlman L.R., Chen D.Y., Gallagher K.M.E., Bauer M.R., Taylor H.B., Dunn W.A., Tarr C., Sidney J., Rachimi S., Conway H.L., Katsis K., Wang Y., Leistritz-Edwards D., Durkin M.R., Tomkins-Tinch C.H., Finkel Y., Nachshon A., Gentili M., Rivera K.D., Carulli I.P., Chea V.A., Chandrashekar A., Bozkus C.C., Carrington M., Bhardwaj N., Barouch D.H., Sette A., Maus M.V., Rice C.M., Clauser K.R., Keskin D.B., Pregibon D.C., Hacohen N., Carr S.A., Abelin J.G., Saeed M., Sabeti P.C. Profiling SARS-CoV-2 HLA-I peptidome reveals T cell epitopes from out-of-frame ORFs. Cell. 2021;184:3962–3980. doi: 10.1016/j.cell.2021.05.046. e17. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wagner K.I., Mateyka L.M., Jarosch S., Grass V., Weber S., Schober K., Hammel M., Burrell T., Kalali B., Poppert H., Beyer H., Schambeck S., Holdenrieder S., Strötges-Achatz A., Haselmann V., Neumaier M., Erber J., Priller A., Yazici S., Roggendorf H., Odendahl M., Tonn T., Dick A., Witter K., Mijočević H., Protzer U., Knolle P.A., Pichlmair A., Crowell C.S., Gerhard M., D'Ippolito E., Busch D.H. Recruitment of highly cytotoxic CD8+ T cell receptors in mild SARS-CoV-2 infection. Cell Rep. 2022;38 doi: 10.1016/j.celrep.2021.110214. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Habel J.R., Nguyen T.H.O., van de Sandt C.E., Juno J.A., Chaurasia P., Wragg K., Koutsakos M., Hensen L., Jia X., Chua B., Zhang W., Tan H.-X., Flanagan K.L., Doolan D.L., Torresi J., Chen W., Wakim L.M., Cheng A.C., Doherty P.C., Petersen J., Rossjohn J., Wheatley A.K., Kent S.J., Rowntree L.C., Kedzierska K. Suboptimal SARS-CoV-2-specific CD8+ T cell response associated with the prominent HLA-A*02:01 phenotype. Proc. Natl. Acad. Sci. 2020;117:24384–24391. doi: 10.1073/pnas.2015486117. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Titov A., Shaykhutdinova R., Shcherbakova O.V., Serdyuk Y.V., Sheetikov S.A., Zornikova K.V., Maleeva A.V., Khmelevskaya A., Dianov D.V., Shakirova N.T., Malko D.B., Shkurnikov M., Nersisyan S., Tonevitsky A., Khamaganova E., Ershov A.V., Osipova E.Y., Nikolaev R.V., Pershin D.E., Vedmedskia V.A., Maschan M., Ginanova V.R., Efimov G.A. Immunogenic epitope panel for accurate detection of non-cross-reactive T cell response to SARS-CoV-2. JCI Insight. 2022;7 doi: 10.1172/jci.insight.157699. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schulien I., Kemming J., Oberhardt V., Wild K., Seidel L.M., Killmer S., Sagar, Daul F., Salvat Lago M., Decker A., Luxenburger H., Binder B., Bettinger D., Sogukpinar O., Rieg S., Panning M., Huzly D., Schwemmle M., Kochs G., Waller C.F., Nieters A., Duerschmied D., Emmerich F., Mei H.E., Schulz A.R., Llewellyn-Lacey S., Price D.A., Boettler T., Bengsch B., Thimme R., Hofmann M., Neumann-Haefelin C. Characterization of pre-existing and induced SARS-CoV-2-specific CD8+ T cells. Nat. Med. (N. Y., NY, U. S.) 2021;27:78–85. doi: 10.1038/s41591-020-01143-2. [DOI] [PubMed] [Google Scholar]
- Swaminathan S., Lineburg K.E., Ambalathingal G.R., Crooks P., Grant E.J., Mohan S.V., Raju J., Panikkar A., Le Texier L., Tong Z.W.M., Chew K.Y., Neller M.A., Short K.R., Gowda H., Gras S., Khanna R., Smith C. Limited recognition of highly conserved regions of SARS-CoV-2. Microbiol. Spectr. 2022;10 doi: 10.1128/spectrum.02780-21. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ferretti A.P., Kula T., Wang Y., Nguyen D.M.V., Weinheimer A., Dunlap G.S., Xu Q., Nabilsi N., Perullo C.R., Cristofaro A.W., Whitton H.J., Virbasius A., Olivier K.J., Jr., Buckner L.R., Alistar A.T., Whitman E.D., Bertino S.A., Chattopadhyay S., MacBeath G. Unbiased screens show CD8+ T cells of COVID-19 patients recognize shared epitopes in SARS-CoV-2 that largely reside outside the spike protein. Immunity. 2020;53:1095–1107. doi: 10.1016/j.immuni.2020.10.006. e3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nelde A., Bilich T., Heitmann J.S., Maringer Y., Salih H.R., Roerden M., LÃbke M., Bauer J., Rieth J., Wacker M., Peter A., HÃrber S., Traenkle B., Kaiser P.D., Rothbauer U., Becker M., Junker D., Krause G.r., Strengert M., Schneiderhan-Marra N., Templin M.F., Joos T.O., Kowalewski D.J., Stos-Zweifel V., Fehr M., Rabsteyn A., Mirakaj V., Karbach J., JÃger E., Graf M., Gruber L.-C., Rachfalski D., Preuß B., Hagelstein I., MÃrklin M., Bakchoul T., Gouttefangeas C.c., Kohlbacher O., Klein R., StevanoviÄ S., Rammensee H.-G., Walz J.S. SARS-CoV-2-derived peptides define heterologous and COVID-19-induced T cell recognition. Nat. Immunol. 2021;22:74–85. doi: 10.1038/s41590-020-00808-x. [DOI] [PubMed] [Google Scholar]
- Schmidt K.G., Nganou-Makamdop K., Tenbusch M., El Kenz B., Maier C., Lapuente D., Überla K., Spriewald B., Bergmann S., Harrer E.G., Harrer T. SARS-CoV-2-seronegative subjects target CTL epitopes in the SARS-CoV-2 nucleoprotein cross-reactive to common cold coronaviruses. Front. Immunol. 2021;12 doi: 10.3389/fimmu.2021.627568. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Somogyi E., Csiszovszki Z., Molnár L., Lőrincz O., Tóth J., Pattijn S., Schockaert J., Mazy A., Miklós I., Pántya K., Páles P., Tőke E.R. A Peptide vaccine candidate tailored to individuals' genetics mimics the multi-targeted T cell immunity of COVID-19 convalescent subjects. Front. Genet. 2021;12 doi: 10.3389/fgene.2021.684152. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhao J., Wang L., Schank M., Dang X., Lu Z., Cao D., Khanal S., Nguyen L.N., Nguyen L.N.T., Zhang J., Zhang Y., Adkins J.L., Baird E.M., Wu X.Y., Ning S., Gazzar M.E., Moorman J.P., Yao Z.Q. SARS-CoV-2 specific memory T cell epitopes identified in COVID-19-recovered subjects. Virus Res. 2021;304 doi: 10.1016/j.virusres.2021.198508. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hu C., Shen M., Han X., Chen Q., Li L., Chen S., Zhang J., Gao F., Wang W., Wang Y., Li T., Li S., Huang J., Wang J., Zhu J., Chen D., Wu Q., Tao K., Pang D., Jin A. Identification of cross-reactive CD8+ T cell receptors with high functional avidity to a SARS-CoV-2 immunodominant epitope and its natural mutant variants. Genes Dis. 2022;9:216–229. doi: 10.1016/j.gendis.2021.05.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jin X., Ding Y., Sun S., Wang X., Zhou Z., Liu X., Li M., Chen X., Shen A., Wu Y., Liu B., Zhang J., Li J., Yang Y., Qiu H., Shen C., He Y., Zhao G. Screening HLA-A-restricted T cell epitopes of SARS-CoV-2 and the induction of CD8+ T cell responses in HLA-A transgenic mice. Cell Mol. Immunol. 2021;18:2588–2608. doi: 10.1038/s41423-021-00784-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lee E., Sandgren K., Duette G., Stylianou Vicki V., Khanna R., Eden J.-S., Blyth E., Gottlieb D., Cunningham Anthony L., Palmer S., Subbarao K. Identification of SARS-CoV-2 nucleocapsid and spike T-cell epitopes for assessing T-cell immunity. J. Virol. 2021;95:e02002–e02020. doi: 10.1128/JVI.02002-20. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Poran A., Harjanto D., Malloy M., Arieta C.M., Rothenberg D.A., Lenkala D., van Buuren M.M., Addona T.A., Rooney M.S., Srinivasan L., Gaynor R.B. Sequence-based prediction of SARS-CoV-2 vaccine targets using a mass spectrometry-based bioinformatics predictor identifies immunogenic T cell epitopes. Genome Med. 2020;12:70. doi: 10.1186/s13073-020-00767-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Panikkar A., Lineburg K.E., Raju J., Chew K.Y., Ambalathingal G.R., Rehan S., Swaminathan S., Crooks P., Le Texier L., Beagley L., Best S., Solomon M., Matthews K.K., Srihari S., Neller M.A., Short K.R., Khanna R., Smith C. SARS-CoV-2-specific T cells generated for adoptive immunotherapy are capable of recognizing multiple SARS-CoV-2 variants. PLoS Pathog. 2022;18 doi: 10.1371/journal.ppat.1010339. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kared H., Redd A.D., Bloch E.M., Bonny T.S., Sumatoh H., Kairi F., Carbajo D., Abel B., Newell E.W., Bettinotti M.P., Benner S.E., Patel E.U., Littlefield K., Laeyendecker O., Shoham S., Sullivan D., Casadevall A., Pekosz A., Nardin A., Fehlings M., Tobian A.A.R., Quinn T.C. SARS-CoV-2-specific CD8+ T cell responses in convalescent COVID-19 individuals. J. Clin. Invest. 2021;131 doi: 10.1172/JCI145476. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gangaev A., Ketelaars S.L.C., Isaeva O.I., Patiwael S., Dopler A., Hoefakker K., De Biasi S., Gibellini L., Mussini C., Guaraldi G., Girardis M., Ormeno C.M.P.T., Hekking P.J.M., Lardy N.M., Toebes M., Balderas R., Schumacher T.N., Ovaa H., Cossarizza A., Kvistborg P. Identification and characterization of a SARS-CoV-2 specific CD8+ T cell response with immunodominant features. Nat. Commun. 2021;12:2593. doi: 10.1038/s41467-021-22811-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhang J., Lin H., Ye B., Zhao M., Zhan J., Dong S., Guo Y., Zhao Y., Li M., Liu S., Zhang H., Xiao W., Guo Y., Yue C., Zhang D., Yang M., Zhang J., Quan C., Shi W., Liu X., Liu P., Jiang Y., Wu G., Gao G.F., Liu W.J. One-year sustained cellular and humoral immunities in coronavirus disease 2019 (COVID-19) convalescents. Clin. Infect. Dis. 2022;75:e1072–e1081. doi: 10.1093/cid/ciab884. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Peng Y., Mentzer A.J., Liu G., Yao X., Yin Z., Dong D., Dejnirattisai W., Rostron T., Supasa P., Liu C. Broad and strong memory CD4+ and CD8+ T cells induced by SARS-CoV-2 in UK convalescent individuals following COVID-19. Nat. Immunol. 2020;21:1336–1345. doi: 10.1038/s41590-020-0782-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhang J., Lu D., Li M., Liu M., Yao S., Zhan J., Liu W.J., Gao G.F. A COVID-19 T-cell response detection method based on a newly identified human CD8+ T cell epitope from SARS-CoV-2- Hubei Province, China, 2021. China CDC Wkly. 2022;4:83–87. doi: 10.46234/ccdcw2021.258. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sekine T., Perez-Potti A., Rivera-Ballesteros O., Strålin K., Gorin J.-B., Olsson A., Llewellyn-Lacey S., Kamal H., Bogdanovic G., Muschiol S. Robust T cell immunity in convalescent individuals with asymptomatic or mild COVID-19. Cell. 2020;183:158–168. doi: 10.1016/j.cell.2020.08.017. e14. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Quiros-Fernandez I., Poorebrahim M., Fakhr E., Cid-Arregui A. Immunogenic T cell epitopes of SARS-CoV-2 are recognized by circulating memory and naïve CD8 T cells of unexposed individuals. EBioMedicine. 2021;72 doi: 10.1016/j.ebiom.2021.103610. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Agerer B., Koblischke M., Gudipati V., Montaño-Gutierrez L.F., Smyth M., Popa A., Genger J.W., Endler L., Florian D.M., Mühlgrabner V., Graninger M., Aberle S.W., Husa A.M., Shaw L.E., Lercher A., Gattinger P., Torralba-Gombau R., Trapin D., Penz T., Barreca D., Fae I., Wenda S., Traugott M., Walder G., Pickl W.F., Thiel V., Allerberger F., Stockinger H., Puchhammer-Stöckl E., Weninger W., Fischer G., Hoepler W., Pawelka E., Zoufaly A., Valenta R., Bock C., Paster W., Geyeregger R., Farlik M., Halbritter F., Huppa J.B., Aberle J.H., Bergthaler A. SARS-CoV-2 mutations in MHC-I-restricted epitopes evade CD8+ T cell responses. Sci. Immunol. 2021;6 doi: 10.1126/sciimmunol.abg6461. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Xiao C., Mao L., Wang Z., Gao L., Zhu G., Su J., Chen X., Yuan J., Hu Y., Yin Z., Xie J., Ji W., Niu H., Gao F., Luo O.J., Xiao L., Wang P., Chen G. SARS-CoV-2 variant B.1.1.7 caused HLA-A2+ CD8+ T cell epitope mutations for impaired cellular immune response. iScience. 2022;25 doi: 10.1016/j.isci.2022.103934. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Keller M.D., Harris K.M., Jensen-Wachspress M.A., Kankate V.V., Lang H., Lazarski C.A., Durkee-Shock J., Lee P.-H., Chaudhry K., Webber K., Datar A., Terpilowski M., Reynolds E.K., Stevenson E.M., Val S., Shancer Z., Zhang N., Ulrey R., Ekanem U., Stanojevic M., Geiger A., Liang H., Hoq F., Abraham A.A., Hanley P.J., Cruz C.R., Ferrer K., Dropulic L., Gangler K., Burbelo P.D., Jones R.B., Cohen J.I., Bollard C.M. SARS-CoV-2 specific T-cells are rapidly expanded for therapeutic use and target conserved regions of membrane protein. Blood. 2020;136:2905–2917. doi: 10.1182/blood.2020008488. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nagler A., Kalaora S., Barbolin C., Gangaev A., Ketelaars S.L.C., Alon M., Pai J., Benedek G., Yahalom-Ronen Y., Erez N., Greenberg P., Yagel G., Peri A., Levin Y., Satpathy A.T., Bar-Haim E., Paran N., Kvistborg P., Samuels Y. Identification of presented SARS-CoV-2 HLA class I and HLA class II peptides using HLA peptidomics. Cell Rep. 2021;35 doi: 10.1016/j.celrep.2021.109305. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Minervina A.A., Pogorelyy M.V., Kirk A.M., Crawford J.C., Allen E.K., Chou C.H., Mettelman R.C., Allison K.J., Lin C.Y., Brice D.C., Zhu X., Vegesana K., Wu G., Trivedi S., Kottapalli P., Darnell D., McNeely S., Olsen S.R., Schultz-Cherry S., Estepp J.H., McGargill M.A., Wolf J., Thomas P.G. SARS-CoV-2 antigen exposure history shapes phenotypes and specificity of memory CD8+ T cells. Nat. Immunol. 2022;23:781–790. doi: 10.1038/s41590-022-01184-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lineburg K.E., Grant E.J., Swaminathan S., Chatzileontiadou D.S.M., Szeto C., Sloane H., Panikkar A., Raju J., Crooks P., Rehan S., Nguyen A.T., Lekieffre L., Neller M.A., Tong Z.W.M., Jayasinghe D., Chew K.Y., Lobos C.A., Halim H., Burrows J.M., Riboldi-Tunnicliffe A., Chen W., D'Orsogna L., Khanna R., Short K.R., Smith C., Gras S. CD8+ T cells specific for an immunodominant SARS-CoV-2 nucleocapsid epitope cross-react with selective seasonal coronaviruses. Immunity. 2021;54(5) doi: 10.1016/j.immuni.2021.04.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Prakash S., Srivastava R., Coulon P.-G., Dhanushkodi N.R., Chentoufi A.A., Tifrea D.F., Edwards R.A., Figueroa C.J., Schubl S.D., Hsieh L., Buchmeier M.J., Bouziane M., Nesburn A.B., Kuppermann B.D., BenMohamed L. Genome-wide B cell, CD4+, and CD8+ T cell epitopes that are highly conserved between human and animal coronaviruses, identified from SARS-CoV-2 as targets for preemptive pan-coronavirus vaccines. J. Immunol. 2021;206:2566. doi: 10.4049/jimmunol.2001438. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Deng J., Pan J., Qiu M., Mao L., Wang Z., Zhu G., Gao L., Su J., Hu Y., Luo O.J., Chen G., Wang P. Identification of HLA-A2 restricted CD8+ T cell epitopes in SARS-CoV-2 structural proteins. J. Leukoc. Biol. 2021;110:1171–1180. doi: 10.1002/JLB.4MA0621-020R. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eggenhuizen P.J., Ng B.H., Chang J., Fell A.L., Cheong R.M.Y., Wong W.Y., Gan P.Y., Holdsworth S.R., Ooi J.D. BCG vaccine derived peptides induce SARS-CoV-2 T cell cross-reactivity. Front. Immunol. 2021;12 doi: 10.3389/fimmu.2021.692729. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Swadling L., Diniz M.O., Schmidt N.M., Amin O.E., Chandran A., Shaw E., Pade C., Gibbons J.M., Le Bert N., Tan A.T., Jeffery-Smith A., Tan C.C.S., Tham C.Y.L., Kucykowicz S., Aidoo-Micah G., Rosenheim J., Davies J., Johnson M., Jensen M.P., Joy G., McCoy L.E., Valdes A.M., Chain B.M., Goldblatt D., Altmann D.M., Boyton R.J., Manisty C., Treibel T.A., Moon J.C., van Dorp L., Balloux F., McKnight Á., Noursadeghi M., Bertoletti A., Maini M.K. Pre-existing polymerase-specific T cells expand in abortive seronegative SARS-CoV-2. Nature. 2022;601:110–117. doi: 10.1038/s41586-021-04186-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Le Bert N., Tan A.T., Kunasegaran K., Tham C.Y.L., Hafezi M., Chia A., Chng M.H.Y., Lin M., Tan N., Linster M., Chia W.N., Chen M.I.C., Wang L.-F., Ooi E.E., Kalimuddin S., Tambyah P.A., Low J.G.-H., Tan Y.-J., Bertoletti A. SARS-CoV-2-specific T cell immunity in cases of COVID-19 and SARS, and uninfected controls. Nature. 2020;584:457–462. doi: 10.1038/s41586-020-2550-z. [DOI] [PubMed] [Google Scholar]
- Pan K., Chiu Y., Huang E., Chen M., Wang J., Lai I., Singh S., Shaw R.M., MacCoss M.J., Yee C. Mass spectrometric identification of immunogenic SARS-CoV-2 epitopes and cognate TCRs. Proc. Natl. Acad. Sci. U. S. A. 2021;118 doi: 10.1073/pnas.2111815118. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ma Y., Liu F., Lin T., Chen L., Jiang A., Tian G., Nielsen M., Wang M. Large-scale identification of T-cell epitopes derived from severe acute respiratory syndrome coronavirus 2 for the development of peptide vaccines against coronavirus disease 2019. J. Infect. Dis. 2021;224:956–966. doi: 10.1093/infdis/jiab324. [DOI] [PubMed] [Google Scholar]
- Mateus J., Grifoni A., Tarke A., Sidney J., Ramirez S.I., Dan J.M., Burger Z.C., Rawlings S.A., Smith D.M., Phillips E., Mallal S., Lammers M., Rubiro P., Quiambao L., Sutherland A., Yu E.D., da Silva Antunes R., Greenbaum J., Frazier A., Markmann A.J., Premkumar L., de Silva A., Peters B., Crotty S., Sette A., Weiskopf D. Selective and cross-reactive SARS-CoV-2 T cell epitopes in unexposed humans. Science. 2020;370:89–94. doi: 10.1126/science.abd3871. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhang Y., Yang Z., Tang M., Li H., Tang T., Li G., Zhong Y., Zhang X., Wang X., Wang C. Three specific potential epitopes that could be recognized by T cells of convalescent COVID-19 patients were identified from spike protein. Front. Immunol. 2022;13 doi: 10.3389/fimmu.2022.752622. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tarke A., Coelho C.H., Zhang Z., Dan J.M., Yu E.D., Methot N., Bloom N.I., Goodwin B., Phillips E., Mallal S., Sidney J., Filaci G., Weiskopf D., da Silva Antunes R., Crotty S., Grifoni A., Sette A. SARS-CoV-2 vaccination induces immunological T cell memory able to cross-recognize variants from Alpha to Omicron. Cell. 2022;185:847–859. doi: 10.1016/j.cell.2022.01.015. e11. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Qiu C., Xiao C., Wang Z., Zhu G., Mao L., Chen X., Gao L., Deng J., Su J., Su H., Fang E.F., Zhang Z.J., Zhang J., Xie C., Yuan J., Luo O.J., Huang L.A., Wang P., Chen G. CD8+ T-cell epitope variations suggest a potential antigen HLA-A2 binding deficiency for spike protein of SARS-CoV-2. Front. Immunol. 2021;12 doi: 10.3389/fimmu.2021.764949. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mahajan S., Kode V., Bhojak K., Karunakaran C., Lee K., Manoharan M., Ramesh A., Hv S., Srivastava A., Sathian R., Khan T., Kumar P., Gupta R., Chakraborty P., Chaudhuri A. Immunodominant T-cell epitopes from the SARS-CoV-2 spike antigen reveal robust pre-existing T-cell immunity in unexposed individuals. Sci. Rep. 2021;11:13164. doi: 10.1038/s41598-021-92521-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shimizu K., Iyoda T., Sanpei A., Nakazato H., Okada M., Ueda S., Kato-Murayama M., Murayama K., Shirouzu M., Harada N., Hidaka M., Fujii S.I. Identification of TCR repertoires in functionally competent cytotoxic T cells cross-reactive to SARS-CoV-2. Commun. Biol. 2021;4:1365. doi: 10.1038/s42003-021-02885-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Li L., Chen Q., Han X., Shen M., Hu C., Chen S., Zhang J., Wang Y., Li T., Huang J., Li S., Hao Y., Jin A.T. Cell immunity evaluation and immunodominant epitope T cell receptor identification of severe acute respiratory syndrome coronavirus 2 spike glycoprotein in COVID-19 convalescent patients. Front. Cell Dev. Biol. 2021;9 doi: 10.3389/fcell.2021.696662. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chen Z., Ruan P., Wang L., Nie X., Ma X., Tan Y. T and B cell Epitope analysis of SARS-CoV-2 S protein based on immunoinformatics and experimental research. J. Cell. Mol. Med. 2021;25:1274–1289. doi: 10.1111/jcmm.16200. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rowntree L.C., Petersen J., Juno J.A., Chaurasia P., Wragg K., Koutsakos M., Hensen L., Wheatley A.K., Kent S.J., Rossjohn J., Kedzierska K., Nguyen T.H.O. SARS-CoV-2-specific CD8+ T-cell responses and TCR signatures in the context of a prominent HLA-A*24:02 allomorph. Immunol. Cell Biol. 2021;99:990–1000. doi: 10.1111/imcb.12482. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wu D., Kolesnikov A., Yin R., Guest J.D., Gowthaman R., Shmelev A., Serdyuk Y., Dianov D.V., Efimov G.A., Pierce B.G., Mariuzza R.A. Structural assessment of HLA-A2-restricted SARS-CoV-2 spike epitopes recognized by public and private T-cell receptors. Nat. Commun. 2022;13:19. doi: 10.1038/s41467-021-27669-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chaurasia P., Nguyen T.H.O., Rowntree L.C., Juno J.A., Wheatley A.K., Kent S.J., Kedzierska K., Rossjohn J., Petersen J. Structural basis of biased T cell receptor recognition of an immunodominant HLA-A2 epitope of the SARS-CoV-2 spike protein. J. Biol. Chem. 2021;297 doi: 10.1016/j.jbc.2021.101065. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Heide J., Schulte S., Kohsar M., Brehm T.T., Herrmann M., Karsten H., Marget M., Peine S., Johansson A.M., Sette A., Lütgehetmann M., Kwok W.W., Sidney J., Schulze Zur Wiesch J. Broadly directed SARS-CoV-2-specific CD4+ T cell response includes frequently detected peptide specificities within the membrane and nucleoprotein in patients with acute and resolved COVID-19. PLoS Pathog. 2021;17 doi: 10.1371/journal.ppat.1009842. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Verhagen J., van der Meijden E.D., Lang V., Kremer A.E., Völkl S., Mackensen A., Aigner M., Kremer A.N. Human CD4+ T cells specific for dominant epitopes of SARS-CoV-2 Spike and Nucleocapsid proteins with therapeutic potential. Clin. Exp. Immunol. 2021;205:363–378. doi: 10.1111/cei.13627. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johansson A.M., Malhotra U., Kim Y.G., Gomez R., Krist M.P., Wald A., Koelle D.M., Kwok W.W. Cross-reactive and mono-reactive SARS-CoV-2 CD4+ T cells in prepandemic and COVID-19 convalescent individuals. PLoS Pathog. 2021;17 doi: 10.1371/journal.ppat.1010203. [DOI] [PMC free article] [PubMed] [Google Scholar]
- de Castro M.V., Santos K.S., Apostolico J.S., Fernandes E.R., Almeida R.R., Levin G., Magawa J.Y., Nunes J.P.S., Bruni M., Yamamoto M.M., Lima A.C., Silva M.V.R., Matos L.R.B., Coria V.R., Castelli E.C., Scliar M.O., Kuramoto A., Bruno F.R., Jacintho L.C., Nunes K., Wang J.Y.T., Coelho V.P., Neto M.M., Maciel R.M.B., Naslavsky M.S., Passos-Bueno M.R., Boscardin S.B., Rosa D.S., Kalil J., Zatz M., Cunha-Neto E. Recurrence of COVID-19 associated with reduced T-cell responses in a monozygotic twin pair. Open Biol. 2022;12 doi: 10.1098/rsob.210240. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rammensee H.G., Gouttefangeas C., Heidu S., Klein R., Preuß B., Walz J.S., Nelde A., Haen S.P., Reth M., Yang J., Tabatabai G., Bösmüller H., Hoffmann H., Schindler M., Planz O., Wiesmüller K.H., Löffler M.W. Designing a SARS-CoV-2 T-cell-inducing vaccine for high-risk patient groups. Vaccines (Basel) 2021;9 doi: 10.3390/vaccines9050428. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pogorelyy M.V., Rosati E., Minervina A.A., Mettelman R.C., Scheffold A., Franke A., Bacher P., Thomas P.G. Resolving SARS-CoV-2 CD4+ T cell specificity via reverse epitope discovery. Cell Rep. Med. 2022;3 doi: 10.1016/j.xcrm.2022.100697. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Le Bert N., Clapham H.E., Tan A.T., Chia W.N., Tham C.Y.L., Lim J.M., Kunasegaran K., Tan L.W.L., Dutertre C.-A., Shankar N., Lim J.M.E., Sun L.J., Zahari M., Tun Z.M., Kumar V., Lim B.L., Lim S.H., Chia A., Tan Y.-J., Tambyah P.A., Kalimuddin S., Lye D., Low J.G.H., Wang L.-F., Wan W.Y., Hsu L.Y., Bertoletti A., Tam C.C. Highly functional virus-specific cellular immune response in asymptomatic SARS-CoV-2 infection. J. Exp. Med. 2021;218 doi: 10.1084/jem.20202617. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Piadel K., Haybatollahi A., Dalgleish A.G., Smith P.L. Selection and T-cell antigenicity of synthetic long peptides derived from SARS-CoV-2. J. Gen. Virol. 2022;103 doi: 10.1099/jgv.0.001698. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Woldemeskel B.A., Garliss C.C., Blankson J.N. SARS-CoV-2 mRNA vaccines induce broad CD4+ T cell responses that recognize SARS-CoV-2 variants and HCoV-NL63. J. Clin. Invest. 2021;131 doi: 10.1172/JCI149335. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Low J.S., Vaqueirinho D., Mele F., Foglierini M., Jerak J., Perotti M., Jarrossay D., Jovic S., Perez L., Cacciatore R., Terrot T., Pellanda A.F., Biggiogero M., Garzoni C., Ferrari P., Ceschi A., Lanzavecchia A., Sallusto F., Cassotta A. Clonal analysis of immunodominance and cross-reactivity of the CD4 T cell response to SARS-CoV-2. Science. 2021;372:1336–1341. doi: 10.1126/science.abg8985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Loyal L., Braun J., Henze L., Kruse B., Dingeldey M., Reimer U., Kern F., Schwarz T., Mangold M., Unger C., Dörfler F., Kadler S., Rosowski J., Gürcan K., Uyar-Aydin Z., Frentsch M., Kurth F., Schnatbaum K., Eckey M., Hippenstiel S., Hocke A., Müller M.A., Sawitzki B., Miltenyi S., Paul F., Mall M.A., Wenschuh H., Voigt S., Drosten C., Lauster R., Lachman N., Sander L.E., Corman V.M., Röhmel J., Meyer-Arndt L., Thiel A., Giesecke-Thiel C. Cross-reactive CD4+ T cells enhance SARS-CoV-2 immune responses upon infection and vaccination. Science. 2021;374:eabh1823. doi: 10.1126/science.abh1823. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bartolo, L.; Afroz, S.; Pan, Y. G.; Xu, R.; Williams, L.; Lin, C. F.; Friedman, E. S.; Gimotty, P. A.; Wu, G. D.; Su, L. F. SARS-CoV-2-specific T cells in unexposed adults display broad trafficking potential and cross-react with commensal antigens. bioRxiv 2021. [DOI] [PMC free article] [PubMed]
- Dykema A.G., Zhang B., Woldemeskel B.A., Garliss C.C., Cheung L.S., Choudhury D., Zhang J., Aparicio L., Bom S., Rashid R., Caushi J.X., Hsiue E.H.-C., Cascino K., Thompson E.A., Kwaa A.K., Singh D., Thapa S., Ordonez A.A., Pekosz A., Dâ€Alessio F.R., Powell J.D., Yegnasubramanian S., Zhou S., Pardoll D.M., Ji H., Cox A.L., Blankson J.N., Smith K.N. Functional characterization of CD4+ T cell receptors crossreactive for SARS-CoV-2 and endemic coronaviruses. J. Clin. Invest. 2021;131 doi: 10.1172/JCI146922. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Woldemeskel B.A., Dykema A.G., Garliss C.C., Cherfils S., Smith K.N., Blankson J.N. CD4+ T cells from COVID-19 mRNA vaccine recipients recognize a conserved epitope present in diverse coronaviruses. J. Clin. Invest. 2022;132 doi: 10.1172/JCI156083. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hu W., He M., Wang X., Sun Q., Kuang M. Specific CD8+ TCR repertoire recognizing conserved antigens of SARS-CoV-2 in unexposed population: a prerequisite for broad-spectrum CD8+ T cell immunity. Vaccines (Basel) 2021;9 doi: 10.3390/vaccines9101093. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
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Data Availability Statement
The data that has been used is confidential.

