Table 1.
No. | Studya | Geography (Country) | Total Individuals | Gender (Female/Male) | Median Age (Range) | Disease Severityb (Asymptomatic or Mild) | Disease Severityb (Moderate or Severe) | Blood Collection Time (Days)c | Initial Peptide Selection Procedured | Proteins | Total Peptides Tested | T cell Assay | Total Distinct Epitopes Identified | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | Saini et al.14 | Denmark | 18 | 6/12 | 43.5 (29–82) | 7 | 11 | As close as possible to the first positive test | NetMHCpan-4.1 | all | 2,204 | multimer qualitative binding | 122 | |
2 | Kared et al.15 | Baltimore/ Washington, USA | 30 | 12/18 | 42.5 (19–77) | N/A | N/A | 27–62 after symptom resolution | Grifoni et al.;16 Prachar et al.17 | all | 408 | multimer qualitative binding | 46 | |
3 | Schulien et al.18 | Germany | 26 | 14/12 | 32.5 (24–56) | 26 | 0 | 24 (14–70) after symptom onset | ANN-4.0, SARS-CoV epitopes16 | S, N, M, ORF1ab, ORF3a | 66 | multimer qualitative binding | 37 | |
4 | Poran et al.19 | N/A | 3 | N/A | N/A | N/A | N/A | N/A | HLAthena | all | 23 | multimer qualitative binding | 11 | |
5 | Shomuradova et al.20 | Moscow, Russia | 31 | 16/15 | 35 (17–59) | 21 | 10 | 33 (17–49) after positive test/after disease onset | NetMHCpan-4.0 and identity with SARS-CoV > 60% | S | 13 | multimer qualitative binding | 10 | |
6 | Nielsen et al.21 | Denmark | 203 | 92/111 | 47 (21–79) | 17 | 186 | 44 (14–129) after symptom onset | N/A | S, N, M | 9 | multimer qualitative binding | 9 | |
7 | Chour et al.22 | USA | 2 | 0/2 | 50 (30–70) | 0 | 2 | 6.5 (2–13) post symptom onset | NetMHC-4.0 | S | 96 | multimer qualitative binding | 6 | |
8 | Sekine et al.23 | Sweden | 66 | 14/41 | 51 | 40 | 26 | 53.5 (IQR: 45.5–61) after symptom onset | NetMHCpan-4.1 | all | 13 | multimer qualitative binding | 4 | |
9 | Nguyen et al.24 | Melbourne, Australia | 7 | 1/6 | 32 (19–74) | 6 | 1 | 90 (5–145) after disease onset | overlapping peptide pools and 5 N-specific immunogenic peptides25,18,26,27 | S, N, M | N/A | ICS IFN-γ release; multimer qualitative binding | 3 | |
10 | Rha et al.28 | South Korea | 37 | 18/19 | 46 (21–83) | 23 | 14 | 46 (19–125) after symptom onset | N/A | S, N, M | 8 | multimer qualitative binding | 2 | |
11 | Ferretti et al.26 | New Jersey/Louisiana, USA | 78 | 55/23 | 19.5 (0–80) | 55 | 23 | 49 (11–111) post diagnosis | identification of 20-mer peptides by TScan screen29 followed by NetMHC-4.0 | all | ~240 | Single-allele ELISA IFN-γ; multimer qualitative bindinge | 28 | |
12 | Nelde et al.30 | Germany | 116 | 55/61 | 44 (18–75) | 36 | 80 | 37.7 (19–52) after positive test | SYFPEITHI-1.0, NetMHCpan-4.0 | all | 120 | ICS IFN-γ release; ELISPOT IFN-γ release | 47 | |
13 | Hu et al.31 | Chongqing, China | 37 | 16/21 | 47 (20–67) | 34 | 3 | N/A | NetMHCpan-4.0, SARS-CoV epitopes32,16 | S, N | 78 | ELISPOT IFN-γ release | 15 | |
14 | Habel et al.25 | Melbourne, Australia | 18 | 10/8 | 54 (22–76) | 11 | 7 | 47 (36–102) after disease onset | NetCTLpan, NetMHCpan | S, N, M, ORF1ab | 14 | ICS IFN-γ release | 14 | |
15 | Lineburg et al.33 | Queensland, Australia | 37 | 23/14 | 51 (20–75) | 7 | 5 | 62 (46–124) after positive test | overlapping peptide pools followed by peptide matrix analysis | all | N/A | ICS IFN-γ release | 4 | |
16 | Lee et al.34 | New South Wales, Australia | 2 | N/A | N/A | 0 | 2 | 30–60 after symptom resolution | Network analysis35 followed by NetMHCpan-4.1 and NetMHCIIpan-4.0 | S, N | 2 | ICS IFN-γ release | 2 | |
17 | Tarke et al.36 | San Diego, USA | 99 | 58/41 | 41 (19–91) | 90 | 9 | 67 (3–184) after symptom onset | NetMHCpan-4.0 | all | 7,525 | AIM assay37 | 803 | |
18 | Peng et al.27 | UK | 42 | 16/26 | 57 (20–95) | 28 | 14 | 42 (30–62) after symptom onset | 15- to 18-mer peptides overlapping by 10 residues, SARS-CoV epitopes32 | all except ORF1 | 450 | ELISPOT IFN-γ release | 46f |
Studies reporting precise epitopes along with the cognate HLA information.
Definition of disease severity varies among studies.
IQR, interquartile range.
NetCTLpan,38 NetMHC-4.0,39 NetMHCpan,40 NetMHCpan-4.0,41 NetMHCpan-4.1,42 SYFPEITHI-1.0,43 ANN-4.0,44 and HLAthena.45
Six (of 28) epitopes were identified using multimer qualitative binding.
Only two (of 46) epitopes that were reported as precise epitopes with the cognate HLA information were considered.