One dose of COVID-19 nanoparticle vaccine REVC-128 protects against SARS-CoV-2 challenge at two weeks post-immunization

ABSTRACT

A COVID-19 vaccine that can give early protection is needed to eliminate the viral spread efficiently. Here, we demonstrate the development of a nanoparticle vaccine candidate, REVC-128, in which multiple trimeric spike ectodomains with glycine (G) at position 614 were multimerized onto a nanoparticle. In-vitro characterization of this vaccine confirms its structural and antigenic integrity. In-vivo immunogenicity evaluation in mice indicates that a single dose of this vaccine induces potent serum neutralizing antibody titre at two weeks post-immunization. This is significantly higher than titre caused by trimeric spike protein without nanoparticle presentation. The comparison of serum binding to spike subunits between animals immunized by a spike with and without nanoparticle presentation indicates that nanoparticle prefers the display of spike RBD (Receptor-Binding Domain) over S2 subunit, likely resulting in a more neutralizing but less cross-reactive antibody response. Moreover, a Syrian golden hamster in-vivo model for the SARS-CoV-2 virus challenge was implemented two weeks post a single dose of REVC-128 immunization. The results showed that vaccination protects hamsters against the SARS-CoV-2 virus challenge with evidence of steady body weight, suppressed viral loads and alleviation of tissue damage for protected animals, compared with ∼10% weight loss, high viral loads and tissue damage in unprotected animals. Furthermore, the data showed that vaccine REVC-128 is thermostable at up to 37°C for at least 4 weeks. These findings, along with a history of safety for protein vaccines, suggest that the REVC-128 is a safe, stable and efficacious single-shot vaccine to give the earliest protection against SARS-CoV-2 infection.

Introduction

SARS-CoV-2, the virus causing the COVID-19 pandemic, is a newly emerging virus. SARS-CoV-2 belongs to the coronavirus family, including severe acute respiratory syndrome coronavirus (SARS, 2003 strain), Middle East respiratory syndrome (MERS) and others causing the common cold. The development of vaccine candidates focuses on the spike (S) protein of the SARS-CoV-2 virus, which forms homotrimers protruding from the virus surface and mediates virus entry by targeting angiotensin receptor 2 (ACE2) as the receptor [1] and heparin as the co-receptor. S protein comprises two functional subunits: S1 for receptor binding and S2 for mediating fusion of the viral and cellular membranes (Figure 1(A)). For SARS-CoV-2, S protein is cleaved at the boundary (S1/S2) between S1 and S2, which remains non-covalently bound in the prefusion conformation [2] (Figure 1(B)). The S1 subunit comprises the N-terminal domain (NTD) and receptor-binding domain (RBD), while the S2 subunit contains the fusion machinery with fusion peptide (FP) located downstream of the cleavage site (Figure 1(A)). The second cleavage at the S2’ site within the S2 subunit leads to a conformational change to initiate the membrane fusion [3] (Figure 1(A)). The discovery of neutralizing monoclonal antibodies (nAbs) reveals several vulnerable sites of the virus. Currently, most of the discovered nAbs target the RBD [4,5] and NTD [4,6], in contrast to a small number of nAbs target the S2 subunit [6]. In particular, the footprint of the most potent nAbs usually lines within the epitope for ACE2 binding on the RBD, suggesting that RBD is a desirable neutralizing epitope on virus spike protein.

Figure 1.

SARS-CoV-2 spike ectodomain and nanoparticle presenting trimeric spike ectodomain. (A) Schematic of SARS-CoV-2 spike protein ectodomain. NTD: N-terminal domain; RBD: receptor-binding domain; S1/S2= S1/S2 protease cleavage site; FP= fusion peptide; HR= heptad repeat. Two arrows indicate the cleavage sites. The native furin cleavage site was knocked out (RRAR→SGAG), two proline at positions K986 and V987 substituted, and one glycine at position D614 substituted for ectodomain expression and nanoparticle conjugation. (B) Schematic of prefusion conformation of SARS-CoV-2 trimeric S structure with NTD, RBD and S2 subunit highlighted in blue, green and grey on one protomer, respectively (PDB:6VSB). (C) Size-exclusion chromatography (SEC) profiles of spike NP (red) and spike non-NP (blue) presentation on a Superose 6 column. (D) Spike NP observation by negative stain EM. In the raw micrograph, the representative of nanoparticle single particle, spike NP aggregates and NPs with varying stoichiometries was circled in blue, yellow and red, respectively. The closer observation of a selected multivalent spike NP is on the right. The grey scale bar represents 200 nm. (E) 2D classes averages of spike NP. The pictures show varying numbers of spike proteins on NPs. (F) Spike trimers are in the desired prefusion conformation on NP.

As an RNA virus, SARS-CoV-2, constantly mutates, as observed during this on-going pandemic. During the first few months of its emergence, one mutation at residue 614 from aspartic acid (D) to glycine (G) on spike protein increased ∼10-fold viral infectivity and became the predominant isolate circulating in the USA and worldwide, as described in the middle of 2020 [7–9]. Recently, the emergence of variants posed an increased risk to public health and defined as Variants of Concern by WHO and CDC [10], including B.1.1.7 (Alpha strain) initially isolated in the UK, B.1.351 (Beta strain) in South Africa, B.1.617.2 (Delta strain) in India and P.1 (Gamma strain) in Brazil. These variants have many mutations leading to increased viral transmissibility (Alpha and Delta strain) [10,11], increased propensity of viral re-infection (Gamma strain) [12], or resistance to vaccine-induced immunity (Beta and Delta strain) [13].

Vaccines with a multivalent display of antigen induce longer-lasting immunity than monovalent antigens [14]. Multivalent display, using virus-like particle (VLP) or nanoparticle (NP), is the common strategy for vaccine development, such as the VLP comprising an array of 360 copies of the L1 capsid protein for the licensed HPV vaccine [15], or the eOD-GT8 60mer HIV-1 vaccine currently in clinical trials [16]. Spike protein or RBD of SARS-CoV-2 conjugated on NP elicited potent neutralizing antibody responses [17,18]. The Novavax COVID-19 nanoparticle vaccine, NVX-CoV2373, gave protection for mice [19] and macaques [20] against viral challenge and showed 89.3% efficacy in Phase III clinical trial conducted in the UK, using a two-dose regimen. Helicobacter pylori ferritin has been used to display antigens from influenza [21], hepatitis C virus [22], HIV-1 [23], Epstein–Barr virus [24] and SARS-CoV-2 [25]. Ferritin is a highly conserved protein with a 24-subunit protein shell, and influenza ferritin vaccines are safe in clinical trials (NCT03186781 and NCT03814720). Very recently, Powell et al. [25] reported that ferritin display of SARS-CoV-2 spike ectodomain can induce a potent neutralizing antibody response in mice, and Saunders et al. [26] reported that ferritin display of RBD elicits cross-neutralizing antibody responses in monkeys. Compared to the RBD vaccine, the spike vaccine contains an NTD subunit that is still a target of protective immunity [27], therefore, has the advantage of preventing breakthrough infections.

In this study, we developed a COVID-19 nanoparticle vaccine, designated as REVC-128 (or spike NP) with trimeric spike ectodomain subunits (glycine substitution at residue 614) multimerized onto the ferritin nanoparticle. The design of this vaccine aims to preferentially present the neutralizing antibody epitope (RBD) but occlude the S2 subunit to the immune system. Such design elicits the neutralizing antibody response over cross-reactive antibody, which might minimize antibody-dependent enhancement (ADE) concern (see Discussion section). We compared the immunogenicity of spike NP versus spike non-NP (soluble trimeric spike protein without nanoparticle presentation) and observed that a single dose of spike NP induced significantly higher neutralizing but less S2 subunit-specific or cross-reactive antibody titres than spike non-NP in mice. Encouraged by observing a high neutralizing antibody titre (10⁴ ID₅₀ of serum dilution) induced by spike NP at two weeks post-immunization, we sought to evaluate the protective efficacy of a one-dose regimen with virus challenge. The in vivo protection efficacy study in hamsters showed that vaccinated animals slightly gained body weight from 4 days post-infection, while the sham group lost ∼10% weight by 7 days post-infection. To the best of our knowledge, REVC-128 is the first COVID-19 vaccine to show evidence of vaccine-induced protection starting at two weeks post-immunization in this virus challenge model, which is earlier than other vaccine candidates showing induced protection starting at or after four weeks post the first dose of immunization (see Discussion section).

Materials and methods

Protein expression and purification

The ectodomain (residues 1-1208) of the spike protein of SARS-CoV-2 was modified based on the GenBank sequence of MN908947, including a glycine substitution at residue 614, an “SGAG” substitution at the furin cleavage site (residues 682–685) and two proline substitutions at residues 986 and 987. A C-terminal T4 fibritin trimerization motif, an HRV3C protease cleavage site and an 8 × His Tag and a TwinStrep Tag were conjugated with the ectodomain of spike protein. The ectodomain of spike protein was also conjugated with ferritin nanoparticles (NP) with a linker of GGGGS to generate spike NP. The sequence was cloned into the mammalian expression vector pCAGGS. The trimeric ectodomain of spike protein of SARS-CoV-2 B.1.351 variant was constructed in the same way, except for the following mutations [13]: L18F, D80A, D215G, L242-244del, R246I, K417N, E484 K, N501Y, D614G, and A701 V. The trimeric ectodomain of spike protein of SARS (2003 strain) was modified based on GenBank sequence of AY278554, including two proline substitutions at residues 968 and 969 [28], same trimerization motif, HRV3C cleavage site and tags. The trimeric ectodomain of spike protein of MERS was modified based on GenBank sequence of JX869059, including furin cleavage site knockout, two proline substitutions at residues 1060 and 1061 [29], same trimerization motif, HRV3C cleavage site and tags.

To express trimeric S2 subunit of spike protein, residues 686-1208 of SARS-CoV-2 were cloned upstream of a C-terminal T4 fibritin trimerization motif, an HRV3C protease cleavage site, an 8 × His Tag and a TwinStrep Tag. Residues 319-541 of SARS-CoV-2 were cloned with C-terminal 6 × His Tag for RBD. Similarly, residues 14-305 of SARS-CoV-2 were cloned with C-terminal 6 × His Tag for NTD.

These expression vectors were codon-optimized and confirmed by sequencing before being transiently transfected into FreeStyle™ 293F cells (Thermo Fisher). Protein was purified from filtered cell supernatants using StrepTactin resin (IBA) or cOmplete His-Tag Purification Resin (Roche) or Jacalin (Thermo Fisher). The purified protein was subjected to additional purification or analysis by size-exclusion chromatography using a Superose 6 column.

Plasmids, encoding the heavy and light chains of CR3022, COVA1-16, COVA1-18, COVA1-22, B38, CA1, CB6, H4, 4A8 and RV82 in a human IgG1 expression vector [30], were transiently transfected into FreeStyle™ 293F cells and purified, as described previously [30]. To express antibody Fab, the heavy chain variable domain was inserted into Fab expression vector containing a 6 × His Tag, as previously described [31], followed by co-transfection with the light chain expression vector. Fab was purified from cell culture supernatant by cOmplete His-Tag Purification Resin (Roche).

ELISA binding assays

Proteins of trimeric spikes of SARS, MERS, or SARS-CoV-2 or RBD, NTD and S2 subunits of SARS-CoV-2 were coated onto 96-well Maxisorb ELISA plates at 200 ng/well diluted in PBS overnight at 4°C. The following day, the plates were washed four times with 300 μL of 1 × PBST (0.05% Tween-20) and blocked with blocking buffer (2% dry milk/5% fetal bovine serum in PBS) for 1 h at 37°C. After blocking, plates were washed, as described above before adding mAbs diluted into the same blocking buffer starting from 10 µg/ml or heat-inactivated animal serum starting from 100-fold dilution with 5-fold serial dilutions for 1 h at 37°C. After incubation, plates were washed and a 1:5000 dilution of Goat anti-human or anti-mouse IgG-HRP conjugate (Jackson ImmunoResearch) in PBST was added for 1 h at room temperature. The bound mAb was detected by adding 100 μl/well of 3,3′,5,5′-Tetramethylbenzidine (TMB) substrate (Life Technologies) and incubating at room temperature for 5 min before the addition of 100 μl of 3% H₂SO₄ to stop the reaction. The optical density (OD) was measured at 450 nm.

Biolayer interferometry

Biolayer light interferometry (BLI) was used with an Octet RED96 instrument (ForteBio, Pall Life Sciences), as described previously [30,31]. Antibody Fab was captured onto anti-human Fab-CH1 biosensors at a concentration of 10 μg/ml as ligand. The tested samples of spike NP or non-NP were diluted in 7 × 2-fold series starting from 250 nM to 3.9 nM in solution. Briefly, biosensors, pre-hydrated in binding buffer (1× PBS, 0.01% BSA and 0.2% Tween-20) for 10 min, were first immersed in the binding buffer for 60 s to establish a baseline followed by submerging in a solution containing ligand for 60 s to capture ligand. The biosensors were then submerged in the binding buffer for a wash for 60 s. The biosensors were then immersed in a solution containing various tested samples as analytes for 120 s to detect analyte/ligand association, followed by 120 s in the binding buffer to assess analyte/ligand dissociation. Binding affinity constants (dissociation constant, K_D; on-rate, k_on; off-rate, k_off) were determined using the Octet Analysis software.

VSV-spike pseudovirus production and neutralization assay

To generate SARS-CoV-2 spike VSV pseudovirus, a plasmid encoding SARS-CoV-2 spike harbouring a C-terminal 18-residue truncation was transfected into pre-seeded 293T cells. Spike sequences are from Wuhan strain (WT), or with D614G mutation, or B.1.351 (Beta) strain with the aforementioned mutations. Spike sequence from B.1.1.7 (Alpha strain) contains the following mutations: ΔH69/V70, ΔY144, N501Y, A570D, D614G, P681H, T716I, S982A and D1118H. Spike sequence from B.1.617.2 (Delta strain) contains the following mutations: T19R, K77R, G142D, Δ156-157, R158G, A222V, L452R, T478K, D614G, P681R and D950N. The next day, transfected cells were infected with VSV (G*ΔG-luciferase) (Kerafast) at an MOI of 3 infectious units/cell. The cell supernatant, containing SARS-CoV-2 pseudotyped VSV, was collected at day 2 post-transfection, centrifuged to remove cellular debris, aliquoted and frozen at −80°C.

Neutralization assays, using the above SARS-CoV-2 pseudotyped VSV, were performed, as previously described [32] with modification. The produced pseudovirus was first titrated with duplicate on Vero E6 cells cultured in EMEM supplemented with 10% fetal bovine serum and 100 I.U./mL penicillin and 100 μg/mL streptomycin at 37°C. The dilution of pseudovirus to achieve 1000-fold luciferase signal higher than background was selected for neutralization assay. In neutralization assay, the heat-inactivated serum starting from 100-fold dilution with serial dilutions was incubated with diluted pseudotyped virus in EMEM for 1 h at 37°C before infecting Vero E6 cells at 37°C, 5% CO₂ for 1 h. The next day, cells were lysed with Passive Lysis Buffer (Promega) for 40 min at room temperature with shaking before adding the Luciferase Activating Reagent (Promega). The luminesce was read immediately on a Molecular Devices reader. Per cent neutralization was calculated based on wells containing virus only and cells only as background. Data were fit to a 4PL curve in GraphPad Prism 7.

Plaque reduction neutralization test (PRNT)

Authentic virus neutralization was measured using SARS-CoV-2 WA1/2020 (Bioqual Lot No. 080420-900; expanded from seed stock # TVP 23156 obtained from UTMB). Briefly, Vero E6 cells were plated in 24-well plates at 3.5 × 10⁵ cells/well in DMEM supplemented with 10% fetal bovine serum and Gentamicin (diluent), until cells reached 80–90% confluency in the following day. Hamster sera collected on Day 13 were heat-inactivated, performed with a serial dilution starting from 20-fold dilution and incubated with 30 pfu of SARS-CoV-2 WA1/2020 for 1 h, before the addition to cells. Cells were overlaid with methylcellulose media for 3 days, fixated with ice-cold methanol at −20°C for 30 min and stained with 0.2% crystal violet for additional 30 min at room temperature. The plates were washed and dried for 15 min. The plaques in each well were recorded and the IC₅₀ titre was calculated.

Negative stain electron microscopy

Negative stain electron microscopy (nsEM) was used, as previously described [33]. Briefly, spike NP was added to 400 square copper mesh grids coated with carbon and stained with 2% uranyl formate. The grids were imaged on a 120 keV Tecnai Spirit electron microscope using an Eagle 4k × 4k CCD camera. NP particles were manually selected from the raw micrograph stacked with a box size of 200 pixels and aligned using iterative MRA/MSA [34]. Single particles were picked with DogPicker and processed in RELION 3.0.

Animal experiments

Animal experiments were done in compliance with all pertinent US National Institutes of Health regulations and approval from the Animal Care and Use Committee (ACUC) of Noble Life Sciences and Bioqual. For the immunogenicity study, 6- to 8-week-old female C57BL/6 mice (Jackson Laboratory) were inoculated subcutaneously in two sites. Each animal received a single dose of 20 µg protein immunogen in 100 µl of PBS, containing 50 µl of the Sigma Adjuvant System (Sigma) with the immunogen and adjuvant mixture following the manufacture’s manual. For serum preparation, blood samples were collected retro-orbitally on days 0, 14 and 28. For the protection efficacy study conducted at Bioqual, 7-week-old male and female Syrian golden hamsters were inoculated intramuscularly into each hind leg. Each animal received a single dose of 100 µg protein immunogen in 200 µl of PBS containing 100 µl of the same adjuvant. For serum preparation, blood samples were collected retro-orbitally on days 0 and 13. On day 14, all animals were challenged with 1.99 × 10⁴ TCID₅₀ of SARS-CoV-2 virus (USA-WA1/2020, NR-53780 BEI Resources). Virus was administered as 100 μl by the intranasal route (50 μl into each nostril). Body weights were assessed daily. All animals were sacrificed on 7 dpi for tissue analyses. Challenge studies were conducted under maximum containment in an animal biosafety level 3 facility under ACUC-approved protocol in compliance with the Animal Welfare Act and other federal statutes and regulations relating to animals and experiments, involving animals.

Quantitative RT-PCR assay for SARS-CoV-2 RNA

The amounts of RNA copies per gram tissue were measured using a qRT-PCR assay, as described previously [35]. Briefly, viral RNA was extracted from the lung and nares collected on 7 dpi with RNA-STAT 60 (Tel-test “B”)/chloroform, precipitated and resuspended in AVE Buffer (Qiagen). To control the amplification reaction, RNA was isolated from the applicable virus stock using the same procedure. RT-PCR assays were performed using TaqMan RT-PCR kit (Bioline, BIO-78005) with primers and probe sequences, described previously [35]. The signal was compared to the known standard curve and calculated to give copies per gram (g). All samples were tested in triplicate.

Quantitative RT-PCR assay for SARS-CoV-2 subgenomic RNA

SARS-CoV-2 subgenomic mRNA (sgRNA) was determined, as described previously [35] with modification. Briefly, the above-extracted RNA was first reverse-transcribed using Superscript III VILO (Invitrogen), following the manufacturer’s instructions. A Taqman custom gene expression assay (ThermoFisher Scientific) was designed using the N gene sgRNA. Reactions were performed on a QuantStudio 6 and 7 Flex Real-Time PCR System (Applied Biosystems) with the following primers and probe sequences. Standard curves, generated using SARS-CoV-2 N gene sgRNA pre-cloned into an expression plasmid, were used to calculate sgRNA in copies per gram. All samples were tested in triplicate.

Subgenomic RNA primers:

• SG-N-F: CGATCTCTTGTAGATCTGTTCTC

• SG-N-R: GGTGAACCAAGACGCAGTAT

• Probe: FAM/TAACCAGAA/ZEN/TGGAGAACGCAGTGGG/IABkFQ

Histopathology

Hamsters were euthanized for necropsy on 7 dpi. The lung and nares were collected in 10% neutral buffered formalin (NBF), fixed and processed to haematoxylin and eosin (H&E)-stained slides and examined by a board-certified pathologist. Qualitative and semi-quantitative assessments were performed, as described previously [36]. Industry best practices [37] and terminology for data capture were consistent with International Harmonization of Nomenclature and Diagnostic Criteria (INHAND) [38].

Severity grading scale

The severity of the non-neoplastic tissue lesions is graded as follows:

Grade 1 (1+): Minimal. This corresponds to a histopathologic change ranging from inconspicuous to barely noticeable but so minor, small, or infrequent to warrant no more than the least assignable grade. For multifocal or diffusely distributed lesions, this grade was used for processes where less than approximately10% of the tissue in an average high-power field was involved. For focal or diffuse hyperplastic/hypoplastic/atrophic lesions, this grade was used when the affected structure or tissue had undergone a less than approximately 10% increase or decrease in volume.

Grade 2 (2+) Mild. This corresponds to a histopathologic change that is a noticeable but not a prominent feature of the tissue. For multifocal or diffusely distributed lesions, this grade was used for processes where approximately 10% and 25% of the tissue in an average high-power field was involved. For focal or diffuse hyperplastic/hypoplastic/atrophic lesions, this grade was used when the affected structure or tissue had undergone an approximately 10% to 25% increase or decrease in volume.

Grade 3 (3+): Moderate. This corresponds to a histopathologic change that is a prominent but not a dominant feature of the tissue. For multifocal or diffusely distributed lesions, this grade was used for processes where approximately 25% and 50% of the tissue in an average high-power field was involved. For focal or diffuse hyperplastic/hypoplastic/atrophic lesions, this grade was used when the affected structure or tissue had undergone an approximately 25% to 50% increase or decrease in volume.

Grade 4 (4+): Marked. This corresponds to a histopathologic change that is a dominant but not an overwhelming feature of the tissue. For multifocal or diffusely distributed lesions, this grade was used for processes where approximately 50% and 95% of the tissue in an average high-power field was involved. For focal or diffuse hyperplastic/hypoplastic/atrophic lesions, this grade was used when the affected structure or tissue had undergone an approximately 50% to 95% increase or decrease in volume.

Grade 5 (5+): Severe. This corresponds to a histopathologic change that is an overwhelming feature of the tissue. For multifocal or diffusely distributed lesions, this grade was used for processes where greater than approximately 95% of the tissue in an average high-power field was involved. For focal or diffuse hyperplastic/hypoplastic/atrophic lesions, this grade was used when the affected structure or tissue had undergone a greater than approximately 95% increase of decrease in volume.

Statistical analysis

ELISA, nAb titre or viral load statistical analyses of the comparison between spike NP and non-NP or sham-immunized animal sera were performed using the Mann–Whitney test with * p < 0.05, ** p < 0.01. Correlation statistical analyses between ELISA and nAb titres were performed using the Spearman nonparametric test with * p < 0.05, *** p < 0.001. The statistical analysis of comparison of body weight change at each time point between animals with spike NP and mock immunized was performed using the two-way ANOVA test with * p < 0.05, ** p < 0.01, *** p < 0.001 using GraphPad Prism version 8.

Results

Generation of trimeric spike protein with or without nanoparticle presentation

We first expressed SARS-CoV-2 spike ectodomain residues 1 to 1208 in trimeric form by appending a T4 fibritin trimerization motif to the c-terminus of spike ectodomain. The ectodomain contains a glycine substitution at residue 614 to match predominant viral isolate circulating in the middle of 2020 [7–9], a “SGAG” substitution at the furin cleavage site (residues 682-685) to knockout furin cleavage, and two proline substitutions at residues 986 and 987 to increase stability [39] (Figure 1(A)). The trimeric ectodomain protein was further multimerized onto ferritin with a linker to generate a nanoparticle (NP), presenting a trimeric spike protein. Trimeric spike proteins with or without NP presentation were referred to spike NP (also designated as REVC-128) or spike non-NP, respectively, in the following. We first characterized spike NP or spike non-NP on size-exclusion chromatography (SEC) with overlapping profiles, showing that spike NP (red) was significantly larger than spike non-NP (blue) (Figure 1(C)). Spike NP displayed a clear, sharp peak, while spike non-NP displayed two peaks that we assigned to a minor aggregates peak and a predominant trimer fraction peak (Figure 1(C)). Negative stain electron microscopy (nsEM) was used to further evaluate the conformational integrity of spike NP proteins. Imaging of spike NP revealed the forms of single particles (blue circled), spike NP aggregates (yellow circled) and spike NPs with varying stoichiometries (red circled), with the latter being the most predominant (Figure 1(D)). Most of stoichiometries ranged from 2 to 9 spike proteins., One representative particle is shown in Figure 1(D). The closer evaluation of spike proteins further validated the order and pre-fusion homogeneity of the spikes on the NPs (Figure 1(E and F)). Consistent with our vaccine design, these nsEM observations validated that the arrangement of spike proteins on the NP sterically blocks S2 subunits by the proximity of adjacent spikes (Figure 1(B)), and this blockage depends on the occupancy rate of the spikes on the NP.

In-vitro characterization and comparison of spike NP and non-NP

Ideally, trimer mimetics of the native spike on NP or itself should present all epitopes recognized by the neutralizing antibodies (nAbs). To characterize the antigenic profile of spike trimers, spike NP and spike non-NP were tested for binding to a panel of published nAbs (IgG format), targeting the RBD and NTD [4–6,40], a non-neutralizing antibody CR3022 [41] and an HIV antibody as a negative control in ELISAs. The binding of spike NP or non-NP to all tested IgGs was potent, except for the HIV antibody control (Figure 2(A)). We next sought to compare the binding kinetics of two representative nAbs to spike NP versus non-NP by Bio-Layer Interferometry (BLI). To eliminate the multivalent binding on BLI, we first generated antibody Fab using sequences from nAbs, COVA1-18 (RBD-specific) and COVA1-22 (NTD-specific) [4]. Fabs of COVA1-18 and COVA1-22 were immobilized on anti-human Fab-CH1 sensors and probed with spike NP or non-NP at 7 different concentrations. BLI data showed that both Fabs binding to spike NP had higher affinities (<pM level), compared to spike non-NP (3.54 and 0.033 nM for COVA1-18 and COV1-22 Fabs, respectively). This higher affinity to spike NP was due to the slower dissociation off-rates (Figure 2(B)). Compared to NTD-specific antibody COVA1-22 binding, the difference of binding to RBD-specific antibody COVA1-18 between spike NP and non-NP was more striking (Figure 2(B)), suggesting that spike NP exhibits the RBD more robustly. The overall antigenic profile, determined by ELISA and BLI (Figure 2), confirmed that spike NP and non-NP displayed the favourable epitopes targeted by the tested nAbs.

Figure 2.

Characterize and compare antigenicity of spike NP and spike non-NP. (A) Antibody (IgG format) binding to spike NP protein (left) and spike non-NP (right) in ELISAs with raw curves displayed. Antibodies targeting RBD and NTD were indicated with a control HIV antibody. (B) Kinetics of antibody Fab-spike binding characterization by Bio-Layer Interferometry (BLI). BLI curves were generated with two published antibody Fab format COVA1-18 on the top and COVA1-22 at the bottom, immobilized on anti-human Fab-CH1 sensors, followed by probing with spike NP or non-NP proteins at concentrations of 250, 125, 62.5, 31.3, 15.6, 7.8 and 3.9 nM. Raw and fit curves were labeled in black and red, respectively. Binding kinetic measurements were indicated below the sensograms.

Spike NP was initially stored at −80°C. To understand the stability of spike NP stored at different temperatures, we evaluated the conformational integrity and antigenicity of this protein, when stored at 4°C, 22°C (room temperature, RT), and 37°C for 2 days, 1 week and 4 weeks. Three representative antibodies targeting the RBD, NTD and S2 subunits of SARS-CoV-2 spike protein, and a negative control antibody were used to test binding. As shown in Figure S1(A), spike NP stored at different temperatures for up to 4 weeks displayed binding to selected RBD and NTD-specific antibodies-CB6 and 4A8 [6,40], respectively identical to untreated spike NP protein stored at −80°C although we observed slightly decreased binding to an S2 subunit-specific antibody, RV82. RV82 is a fully human monoclonal antibody (IgG1) identified from a B cell repertoire of COVID-19 convalescent humans and confirmed to bind to monomeric or trimeric S2 subunit proteins of SARS-CoV-2 (Figure S2(A)). Consistently, RV82 retained binding to trimeric spike protein of SARS-CoV-2 B.1.351 variant (Beta strain) that has all mutations located within S1 subunit, while most of the tested RBD- or NTD-specific antibodies showed ablated binding to these mutations, except for CR3022 [41] and COVA1-16 [4] antibodies (Left two, Figure S2(B)). Different from CR3022 and COVA1-16, RV82 is bound to SARS-CoV-2, but not to SARS (2003 strain) (Right, Figure S2(B)). Besides ELISAs, SEC was performed to further evaluate spike NP thermostability. Different amounts of spike NP stored at −80°C, 4°C and 37°C for 4 weeks were loaded onto a Superose 6 column with the overlapping profiles showing that all proteins displayed clear, sharp peaks at the same elution volume (Figure S1(B)). RBD and NTD are the major neutralizing epitopes [4–6,40] and SDS-PAGE analysis of spike NP showed no difference between protein being stored at various temperatures and −80°C (data not shown) suggest that spike NP is stable up to 37°C for at least 4 weeks.

Immunogenicity of spike NP and non-NP in mice

We next evaluated the immunogenicity of spike NP and non-NP in mice. Two groups of mice were immunized with spike NP and spike non-NP with the Sigma Adjuvant System via a subcutaneous injection route, respectively. The third group of mice were injected with PBS as a negative control. We first assessed sera antibody binding collected 14- or 28-days post-immunization to trimeric spike protein with D614G mutation. Significant levels of spike protein-specific IgG were detected in all vaccinated mice 14 days post-immunization and spike NP induced spike-specific IgG ∼1.5-fold higher than spike non-NP on days 14 and 28, with the titre declining on day 28 (Figure 3(A)). Besides trimeric spike protein binding, we assessed the binding of RBD, S2, and NTD subunits to sera collected 14 days post-immunization. The results showed that sera from spike NP immunized mice displayed significantly higher binding to RBD than sera from spike non-NP immunized animals (** p < 0.01, the Mann–Whitney test) (Left, Figure 3(B)), while serum binding to S2 subunit was opposite, with sera from spike non-NP immunized animals showing significantly stronger binding to S2 subunit (** p < 0.01, the Mann–Whitney test) (Middle, Figure 3(B)), indicating NP presentation preferentially exposed RBD over S2 subunit, consistent with vaccine design. NTD-specific antibody responses in all groups were weak on day 14 (Right, Figure 3(B)).

Figure 3.

Immune response to spike NP or non-NP. (A) Wide-type C57BL/6 mice were immunized with 20 µg spike NP or spike non-NP with Sigma Adjuvant System via subcutaneous injection route. The serum was collected 14- and 28-days post immunization and tested to bind to SARS-CoV-2 spike trimeric protein with D614G mutation in ELISAs. ELISA titer was calculated on reciprocal serum dilution to achieve 50% of maximal optical absorbance (OD). Black bars reflect mean responses. (B) The binding of sera collected at day 14 to spike RBD, S2 and NTD subunits of SARS-CoV-2 in ELISAs. Statistical analysis was performed with Mann-Whitney test (** p<0.01). (C) The binding of sera collected at day 14 to trimeric spike protein of SARS (2003 strain) and MERS. Statistical analysis was performed with Mann-Whitney test (* p<0.05). (D) The neutralizing activity of sera collected at days 14 and 28 against VSV pseudotyped virus with SARS-CoV-2 spike protein containing D614G mutation. NAb titer (neutralizing antibody) represents the reciprocal of the antiserum dilution at which virus entry is inhibited by 50%, when calculated after curve-fitting with the Prism program (GraphPad). Black bars reflect mean responses. Statistical analysis was performed with Mann-Whitney test (* p<0.05). (E) The correlate of serum neutralizing titer and ELISA titer of binding to RBD protein (left) or trimeric spike (right). The correlation for day 14 sera between neutralizing titer (log10) and ELISA binding titer (log10) was analyzed using Spearman nonparametric test. Line represents the best fit linear regression.

Cross-reactive and non- or weak neutralizing antibodies are potentially responsible for antibody-dependent enhancement (ADE). To evaluate vaccine-elicited cross-reactive antibodies, we assessed sera collected on day 14 for binding to trimeric spike proteins from the SARS (2003 strain) or MERS. Consistent with S2 subunit binding, sera from spike non-NP immunized animals showed stronger binding to these two different coronavirus spike proteins than sera from spike NP-immunized ones, especially to the MERS spike protein (* p < 0.05, the Mann–Whitney test) (Figure 3(C)). The data suggested spike NP elicited less cross-reactive antibodies that are possibly S2 subunit-specific.

Neutralizing antibodies are related to vaccine-induced protection. Sera collected on days 14 and 28 were tested for neutralizing antibody activity against VSV pseudotyped virus with SARS-CoV-2 spike protein-containing D614G mutation and a luciferase reporter. On day 14, we observed that the neutralizing antibody (nAb) titre of sera from spike NP-immunized mice was on average 4 log (ID₅₀), significantly higher than the titre of sera from spike non-NP-immunized ones (* p < 0.05, the Mann–Whitney test) (Left, Figure 3(D)). Similarly, the neutralizing antibody titre declined on day 28, but the titre of spike NP-immunized sera was still significantly higher than that of spike non-NP-immunized sera (* p < 0.05, Mann–Whitney test) (Right, Figure 3(D)). To assess neutralizing antibody epitope on spike protein, we analysed the correlation between day 14 serum neutralizing titre and ELISA titre obtained from either binding to spike RBD subunit or whole spike protein. This analysis revealed a more correlated relationship between neutralizing titre and RBD binding titre (R = 0.6915, *** p = 0.0007), compared to the correlate with spike binding (R = 0.4537, * p = 0.045) (Figure 3(E)). This indicated RBD is the major neutralizing antibody epitope and RBD-specific nAbs are responsible for serum neutralizing activity. This agrees with the rationale of our vaccine design by using NP to preferentially present RBD, validated by the above BLI results (Figure 2(B)).

Protection efficacy of spike NP in hamsters

Encouraged by the potent immune mouse serum neutralizing antibody response elicited by spike NP that we observed on day 14, we next evaluated vaccine protection efficacy in Syrian golden hamsters, one of few small animal models susceptible to infection by the SARS-CoV-2 virus [35,42]. Two groups of hamsters were immunized with a single dose of spike NP (REVC-128) or sham control, including the same NP presenting Marburg trimeric GP, and the same adjuvant via an intramuscular injection route (Figure 4(A)). We observed that sera collected from spike NP-immunized hamsters on day 13, one day before virus challenge, displayed significantly higher potent neutralizing antibody activity against VSV pseudotyped with SARS-CoV-2 D614G spike than sera from the sham group (* p < 0.05, the Mann–Whitney test) (Left, Figure 4(B)). Besides, we evaluated serum neutralizing antibody activity against VSV pseudotyped with WT spike (Wuhan strain) or spikes with mutations identified in variants. Figure 4(B) shows that a single dose of spike NP-immunized animal sera displayed the similar neutralizing activity against WT, D614G and B.1.1.7 (Alpha) pseudoviruses, but modestly reduced activity against B.1.617.2 (Delta) and significant reduced activity against B.1.351 (Beta) pseudoviruses, similar as two-dose of mRNA vaccine-induced sera [13,43]. Only one animal serum with the most potent neutralizing activity against WT pseudovirus could neutralize B.1.351 pseudovirus with approximately 10-fold titre reduction (Left, Figure 4(B)), suggesting a need of booster to protect against this variant. Besides pseudovirus, authentic virus neutralizing activity of the same sera was assessed with results showing similar differences, but at lower values (Right, Figure 4(B)), consistent with the observation reported by others [44].

Figure 4.

Vaccine protection efficacy against virus challenge in hamsters. (A) Schematic of the immunization and virus challenge protocol. Syrian golden hamsters (2F/2M) were immunized with 100 µg spike NP (REVC-128) or sham with Sigma Adjuvant System via intramuscular injection route, and challenged with 1.99 × 10⁴ TCID₅₀ of SARS-CoV-2 virus (USA-WA1/2020, NR-53780, BEI Resources) by the intranasal route at day 14 post immunization. (B) The neutralizing activity of sera collected at day 13 post immunization against VSV pseudotyped viruses (left) containing SARS-CoV-2 spike with sequence of WT (Wuhan strain), D614G mutation, B.1.1.7 (Alpha strain), B.1.617.2 (Delta strain), or B.1.351 (Beta strain). Results of each serum collected from spike NP immunized animal were connected with lines to compare serum neutralizing activity against these SARS-CoV-2 variants. The same sera were also assessed for neutralization against authentic virus (SARS-CoV-2 WA1/2020 strain) by PRNT (right). Statistical analysis of serum neutralizing D614G pseudovirus between spike NP and mock immunized animals was performed with Mann-Whitney test (* p<0.05). (C) Median percent weight change after challenge. Statistical analysis for body weight change was performed for comparison between spike NP and mock immunized animals by two-way ANOVA test, * p<0.05, ** p<0.01, *** p<0.001. (D) Tissue viral loads on 7 dpi. Viral loads of lung (left) and nares (right) were measured by RT-PCR and quantitated as total viral RNA copies per gram tissue (upper) and subgenomic N RNA copies per gram tissue (bottom). Limitation of quantification is 200 copies/g. Black bars reflect mean responses. Statistical analysis was performed with Mann-Whitney test (* p<0.05). SGN=Subgenomic N RNA copies. (E, F) Representative images of histopathology for lungs (E) and blood vessels (F) of sham control (upper) and spike NP (bottom) immunized animals. In a higher magnification of (E) on right (20 ×), black arrows indicate bronchiolo-alveolar hyperplasia characterized by hyperplastic epithelial cells extending from bronchioles and lining alveoli. Black arrowhead indicates hyperplastic cells with enlarged nuclei. Open arrow indicates mixed cell inflammation observed in alveolar lumen. In (F), black arrow indicates expansion of surrounding vascular tissue by edema (increased clear space and a pale basophilic material) and mononuclear cells. Black arrowhead indicates mononuclear inflammatory cells expanding the vessel wall (tunica media and intima).

Fourteen days post-immunization, animals were challenged with the SARS-CoV-2 virus intranasally. In the sham control, hamsters lost a median of 10% body weight by 7 days post-infection (dpi), while spike NP-immunized animals gained bodyweight lightly from 4 dpi (Figure 4(C)). Significant weight differences post-infection were observed from 4 to 7 dpi (* p < 0.05, ** p < 0.01, *** p < 0.001, two-way ANOVA test) (Figure 4(C)). To determine the impact of vaccine-induced immunity on viral tissue load, we measured viral genomic and subgenomic RNA amounts in the lung and nares collected on 7 dpi. Viral genomic RNA (vRNA) reflects the remaining viral inoculum plus newly replicating virus, while subgenomic RNA (sgRNA) should only result from newly replicating virus [45]. For hamsters immunized by spike NP, we observed significantly lower amounts of viral RNA in the lung and nares (∼3 log) than that in animal tissues in the sham control (Upper, Figure 4(D)). Similarly, the level of sgRNA in protected animals’ tissues was approximately 3 logs lower than that in sham control animals’ tissues (Bottom, Figure 4(D)).

We next performed histopathology analyses of the lungs and nares of two groups of infected hamsters. Qualitative and semi-quantitative analyses of the lung and nares tissues collected on 7 dpi were performed using a severity scoring scale [36] (Table 1). In the sham control, all hamsters showed evidence of pulmonary lesions with the observations of moderate to marked bronchioloalveolar hyperplasia (grade 3 or 4), mild mixed cell bronchioloalveolar inflammation (grade 2) and minimal to mild mononuclear cell perivascular/vascular infiltrate or alveolar/perivascular/vascular inflammation (grade 1 or 2) (Figure 4(E,F) and Table 1). Perivascular oedema (grade 1 or 2), syncytial cells and haemorrhage (grade 1) were observed in the lungs of some but not all animals in the sham control (Figure 4(F) and Table 1). Most animals in the sham control also exhibited atypia of hyperplastic alveolar epithelial cells with hypertrophic and variably shaped nuclei and prominent nucleoli (Figure 4(E)). Syncytial cells, enlarged multinucleated cells, most likely Type II pneumocytes, demonstrating viral cytopathic-like changes, were scattered throughout alveoli in the lungs of animals in sham control. SARS-CoV-2 virus has infected Type I and Type II pneumocyte cells in animal studies [46], and the infection and loss of Type I pneumocytes would proliferate Type II pneumocytes. Overall, the histological observations in the lungs and nares of sham control were consistent with SARS-CoV-2 infection, reported previously [47]. In spike NP immunized animals, one animal showed minimal bronchiolar hyperplasia in the lung (grade 1) and another one showed minimal lesions in nares (grade 1) (Table 1), while the rest of the animals in this group showed negligible histopathologic phenotype.

Table 1.

Macroscopic observation of the lung and nares from spike NP immunized and sham control on 7 dpi.

In summary, weight change, viral load and histopathological data support that REVC-128 effectively protected against COVID-19=associated morbidity starting two weeks post a single dose of immunization.

Discussion

Herein, we developed a COVID-19 protein-based nanoparticle vaccine, REVC-128. Protein-based vaccines, such as the Hepatitis B vaccine that has been administered on the first day of life for newborn babies, have shown minimal safety concern. The backbone of the nanoparticle, ferritin, has also been shown to be safe for influenza vaccines in clinical trials. Therefore, REVC-128 can protect individuals who are medically unable to receive other COVID-19 vaccines, such as people who are allergic to mRNA vaccines. Additionally, the vaccine stability data (Figure S1) support a much less stringent requirement for the storage of this vaccine, compared with mRNA vaccines that require −20°C or −80°C storage. Vaccine storage and transportation in ambient temperature conditions will enable the broader availability of such vaccines.

Vaccination using a one-dose regimen enables easier deployment, tracking and administration, compared to a two-dose regimen. Furthermore, vaccine that can give early protection can more efficiently prevent the viral spread and contribute to the quelling of this COVID-19 pandemic. Herein, we showed that a single dose of REVC-128 provides protection starting two weeks post-immunization, earlier than other vaccine candidates. To the best of our knowledge, two viral vector vaccines (VSV and Ad26) have been reported to induce early protection starting four weeks post-immunization using a one-dose regimen [42,48], while mRNA vaccines (e.g. Moderna, Pfizer/BioNTech), inactivated vaccine (e.g. Sinovac Life Sciences) and another nanoparticle protein vaccine, Novavax’s NVX-CoV2373 that all use a two-dose regimen with the evidence of protection occurring at or after four weeks post the first dose of immunization. Another protein vaccine, SCB-2019, comprising S-Trimer, elicited robust humoral and cellular immune responses using a two-dose regimen [49]. Although viral vector vaccines gave early protection, the pre-existing immunity to viral vectors presents a formidable challenge for this platform, especially when a boosting immunization is required. The booster enhances the immune response to the viral vector, which could impair vector entry into host cells. In contrast, protein or mRNA vaccines avoid this challenge and allow more flexibility for multiple boosts to achieve a more extended protection period or protection against mutant variants. We observed the decreased neutralizing antibody titre on day 28 after a single dose of immunization (Figure 3(D)) and also the enhanced titre following a booster (data not shown). The protection durability and serum neutralizing activity against variants induced by one-dose and two-dose regimens merit further investigation, along with the assessment of vaccine-induced cellular response, including memory B and T cell responses. Besides a two-dose regiment to protect against variants, a single dose of the mixture of NP conjugated spikes from variants or mosaic NP vaccine merits investigation for broad protection. The immunogen dose used in this report is high (20 μg per mouse or 100 μg per hamster), warranting a dose-de-escalating study to assess the optimal dose in the future.

During this COVID-19 pandemic, concerns arose about pre-existing human coronavirus-specific antibodies generated during previous infections. These antibodies may mediate antibody-dependent enhancement (ADE), worsening symptoms when patients are infected with SARS-CoV-2 [50]. This might be one of the reasons why older adults are at higher risk for severe disease, as antibodies previously generated in response to common human coronaviruses in the elderly facilitate SARS-CoV-2 entrance into target cells, leading to more severe symptoms [51]. On the contrary, the seroprevalence of community-acquired coronavirus in paediatrics is not common [52]. In addition, one possible explanation for SARS-CoV-2 reinfection is the antibodies induced by the first infection may help, rather than fight, the second infection, which is linked to ADE [53]. Previous Dengue virus vaccine studies revealed human clinical safety risks related to ADE [54], resulting in vaccine trial failure. The envelope protein sequence alignment of four serotypes of Dengue and Zika viruses (flavivirus family) indicates that envelope protein domain II, containing fusion machinery, exhibits a higher degree of homology among these viruses, and virus infection induces a high level of domain II-specific antibodies that are non- or weakly neutralizing, but responsible for ADE effect. In line with Dengue domain II, the S2 subunit of the SARS-CoV-2 spike protein-containing fusion machinery exhibits a higher degree of homology among coronaviruses than the S1 subunit of the spike protein. It has been reported that antibodies from SARS-CoV-2 naïve donors, who had reactivity to seasonal human coronavirus strains (such as OC43 and HKU1), were cross-reactive against the nucleocapsid and S2 subunit on spike protein of SARS-CoV-2 [4,55]. More studies have reported that cross-reactive mAbs predominantly target this more conserved S2 subunit on spike protein [6,56]. Conceptually, many S2 subunit-specific antibodies are non- or weakly neutralizing and potentially responsible for ADE. Thus, vaccine design to minimize the elicitation of S2 subunit-specific antibodies should be considered, mainly when/if ADE will be observed for SARS-CoV-2.

Although ADE has yet to be fully observed for SARS-CoV-2 infection or vaccination, previous coronavirus vaccine candidates were reported to be complicated by ADE. A viral vector vaccine of the original SARS enhanced the immunopathology of immunized animals following viral challenge, resulting in strong inflammatory response and even lung injury [57]. Mice immunized by Ad5 viral vector expressing MERS vaccine also exhibited pulmonary pathology following viral challenge, despite the vaccine conferring protection [58]. A similar observation was reported for inactivated virus vaccine. Lung immunopathology was observed when animals were immunized with inactivated whole-virus MERS vaccine, followed by virus challenge [59]. One strategy to offset ADE concern of Dengue and Zika vaccines is to reduce cross-reactive antibody response [60]. Similarly, we used adjacent spike proteins on NP to sterically block the S2 subunit exposure, validated with evidence of fewer S2 subunit and cross-reactive antibodies elicited by spike NP, compared with the vaccine without NP (Figure 3(B,C)). The epitope mapping of these cross-reactive antibodies will be performed in the future to assess whether they are S2-specific. Nevertheless, such design might prevent the development of severe symptoms if patients are infected with other coronaviruses post-immunization, such as seasonal coronaviruses (e.g. common cold virus) or mutated SARS-CoV-2 variants.

Funding Statement

This study is partially supported by a fund from The University of Maryland Strategic Partnership (MPower) and the Institute for Bioscience and Biotechnology Research intramural startup fund (YL). This study is also partially supported by a fund from TEDCO (the Maryland Technology Development Corporation) (YW). With the mission to facilitate technology company growth in Maryland, TEDCO enhances economic development growth by fostering an inclusive entrepreneurial innovation ecosystem.

Disclosure statement

No potential conflict of interest was reported by the author(s).