Second-generation COVID-19 vaccines could contribute to establish protective immunity against SARS-CoV-2 and its emerging variants. We developed COH04S1, a synthetic multiantigen modified vaccinia Ankara-based SARS-CoV-2 vaccine that co-expresses spike and nucleocapsid antigens. Here, we report COH04S1 vaccine efficacy in animal models. We demonstrate that intramuscular or intranasal vaccination of Syrian hamsters with COH04S1 induces robust Th1-biased antigen-specific humoral immunity and cross-neutralizing antibodies (NAb) and protects against weight loss, lower respiratory tract infection, and lung injury following intranasal SARS-CoV-2 challenge. Moreover, we demonstrate that single-dose or two-dose vaccination of non-human primates with COH04S1 induces robust antigen-specific binding antibodies, NAb, and Th1-biased T cells, protects against both upper and lower respiratory tract infection following intranasal/intratracheal SARS-CoV-2 challenge, and triggers potent post-challenge anamnestic antiviral responses. These results demonstrate COH04S1-mediated vaccine protection in animal models through different vaccination routes and dose regimens, complementing ongoing investigation of this multiantigen SARS-CoV-2 vaccine in clinical trials.
Since the emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in China at the end of 2019, SARS-CoV-2 has spread rapidly worldwide, causing a global pandemic with millions of fatalities1,2. Several SARS-CoV-2 vaccines were developed in response to the COVID-19 pandemic with unprecedented pace and showed 62–95% efficacy in Phase 3 clinical trials, leading to their emergency use authorization (EUA) in many countries by the end of 2020/beginning of 20213,4,5,6,7,8. This includes vaccines based on mRNA, adenovirus vectors, and nanoparticles that utilize different antigenic forms of the spike (S) protein to induce protective immunity against SARS-CoV-2 primarily through the function of neutralizing antibodies (NAb)9,10,11,12. While the Phase 3 efficacy results provide hope for a rapid end of the COVID-19 pandemic, waning antibody responses and evasion of NAb by emerging variants of concern (VOC) pose imminent challenges for durable vaccine protection and herd immunity13,14,15,16,17,18,19. Alternative vaccines based on different platforms or modified epitope or antigen design could therefore contribute to establish long-term and cross-reactive immunity against SARS-CoV-2 and its emerging VOC.
While NAb blocking S-mediated entry are considered the principal SARS-CoV-2 immune correlate of protection, humoral and cellular immune responses to multiple antigens have been implicated in the protection against SARS-CoV-210,11,20. Besides the S protein, the nucleocapsid (N) protein is well-recognized as a dominant target of antibody and T cell responses in SARS-CoV-2-infected individuals and therefore suggested as an additional immunogen to augment vaccine-mediated protective immunity21,22,23,24. Its high conservation and universal cytoplasmic expression makes the N protein an attractive complementary target antigen to elicit durable and broadly reactive T cells23. Several recent studies highlight the benefits of N as a vaccine antigen in animal models25,26,27,28.
We previously constructed multiantigenic SARS-CoV-2 vaccine candidates using a fully synthetic platform based on the well-characterized and clinically proven Modified Vaccinia Ankara (MVA) vector29,30,31,32, which is marketed in the USA as Jynneos™ (Bavarian-Nordic)33. MVA is a highly attenuated poxvirus vector that is widely used to develop vaccines for infectious diseases and cancer due to its excellent safety profile in animals and humans, versatile delivery and expression system, and ability to stimulate potent humoral and cellular immune responses to heterologous antigens30,31,32. We have used MVA to develop vaccine candidates for preclinical testing in animal models of congenital cytomegalovirus disease while demonstrating vaccine efficacy in several clinical trials in solid tumor and stem cell transplant patients34,35,36,37,38,39. Using the synthetic MVA (sMVA) platform, we constructed sMVA vectors to co-express full-length, unmodified S and N antigen sequences based on the Wuhan-Hu-1 reference strain. Immunization of mice with these vaccine vectors resulted in the stimulation of potent SARS-CoV-2 antigen-specific humoral and cellular immune responses, including potent NAb29. One of these sMVA vector constructs forms the basis of clinical vaccine candidate COH04S1, which has shown to be safe and immunogenic in a randomized, double-blinded, placebo-controlled, single center Phase 1 trial in healthy adults (NCT04639466), and is currently evaluated in a randomized, double-blinded, single center Phase 2 trial in hematology patients who have received cellular therapy (NCT04977024).
In this report, we demonstrate that COH04S1 stimulates protective immunity against SARS-CoV-2 in Syrian hamsters by intramuscular (IM) and intranasal (IN) vaccination and in non-human primates (NHP) through two-dose (2D) and single-dose (1D) vaccination regimens. These results complement the clinical evaluation of this multiantigen sMVA-based SARS-CoV-2 vaccine.
COH04S1 induces robust Th1-biased S and N antigen-specific antibodies and cross-NAb against SARS-CoV-2 in hamsters through IM and IN vaccination
Syrian hamsters are widely used to evaluate vaccine protection against SARS-CoV-2 in a small animal model that mimics moderate-to-severe COVID-19 disease40,41,42,43,44,45. Using this animal model, we assessed efficacy of COH04S1 (Fig. 1a) to protect against SARS-CoV-2 challenge by either IM or IN vaccination to assess vaccine protection via parenteral or mucosal immune stimulation. Hamsters were vaccinated twice in a four-week interval with 1 × 108 plaque forming units (PFU) of COH04S1 by IM or IN route, referred to as COH04S1-IM or COH04S1-IN, respectively (Fig. 1b). Unvaccinated animals and hamsters vaccinated IM or IN with empty sMVA vector were used as controls. COH04S1-IM and COH04S1-IN stimulated robust and comparable binding antibodies to both the S and N antigens, including antibodies to the S receptor binding domain (RBD), the primary target of NAb46,47,48. Binding antibodies to S, RBD, and N were detected at high levels in both the COH04S1-IM and COH04S1-IN vaccine groups after the first vaccination and boosted after the second vaccination (Fig. 1c, d and Supplementary Fig. 1), whereby a particularly strong booster effect was observed for RBD-specific antibodies. Antigen-specific binding antibodies stimulated by COH04S1-IM and COH04S1-IN in hamsters were mainly composed of IgG2/3 isotypes and only to a minor extent of IgG1 isotype (Fig. 1e and Supplementary Fig. 1), indicating Th1-biased immune responses.
Plaque reduction neutralization titer (PRNT) assay measuring neutralizing activity against SARS-CoV-2 infectious virus (USA-WA1/2020) demonstrated that potent and comparable NAb titers were stimulated by COH04S1-IM and COH04S1-IN after the booster vaccinations (Fig. 1f, g). Furthermore, pooled post-boost immune sera from COH04S1-IM and COH04S1-IN-vaccinated animals demonstrated potent cross-reactive neutralizing activity against SARS-CoV-2 pseudoviruses (PV) with D614G S mutation or multiple S modifications based on several SARS-CoV-2 VOC (Fig. 1h, Supplementary Fig. 1, and Supplementary Table 1), including Alpha (B.1.1.7), Beta (B.1.351), Gamma (P.1), and the increasingly dominant Delta variant (B.1.617.2). These results demonstrate that IM and IN vaccination of Syrian hamsters with COH04S1 elicits robust Th1-biased S and N antigen-specific binding antibodies as well as potent NAb responses with cross-reactivity to prevent PV infection by several SARS-CoV-2 VOC.
IM and IN vaccination with COH04S1 protect hamsters from progressive weight loss, lower respiratory tract infection, and lung pathology following SARS-CoV-2 challenge
Two weeks after the booster vaccination, hamsters were challenged IN with 3 × 104 PFU of SARS-CoV-2 reference strain USA-WA1/2020 and body weight changes were measured over a period of 10 days. While control animals showed rapid body weight loss post challenge, hamsters vaccinated IM or IN with COH04S1 were protected from severe weight loss following challenge (Fig. 2a, b). Control animals showed rapid body weight loss for 6–7 days post challenge, reaching maximum weight loss between 10% and 20%. In contrast, COH04S1-IM and COH04S1-IN-vaccinated animals showed no or only very minor body weight decline post challenge, with maximum body weight loss below 4% for all animals at any time point during the entire 10 day observation period (Fig. 2a, b). Notably, while minor weight loss was observed for COH04S1-IM-vaccinated animals at 1–2 days post challenge, COH04S1-IN-vaccinated animals did not show body weight decline at these early time points post challenge (Fig. 2a), suggesting improved protection from weight loss by COH04S1 through IN compared to IM vaccination at an early phase post challenge.
At day 10 post challenge, hamsters were euthanized for viral load assessment and histopathology analysis. Viral load was measured in the lungs and nasal turbinates/wash by quantification of SARS-CoV-2 genomic RNA (gRNA) and sub-genomic RNA (sgRNA) to gauge the magnitude of total and replicating virus at lower and upper respiratory tracts. Compared to lung viral loads of control animals, markedly reduced gRNA and sgRNA copies were observed in the lungs of COH04S1-IM and COH04S1-IN-vaccinated animals (Fig. 2c, d), demonstrating potent vaccine protection against lower respiratory tract infection through IM and IN vaccination. SARS-CoV-2 gRNA copies in the lungs of COH04S1-IM and COH04S1-IN-vaccinated animals were more than three to four orders of magnitude lower than in the lungs of control animals. Furthermore, while 103-106 sgRNA copies were detected in the lungs of control animals, sgRNA was undetectable in the lungs of COH04S1-IM and COH04S1-IN-vaccinated animals, indicating complete absence of replicating virus in lung tissue of vaccinated hamsters. Compared to nasal viral loads of controls, gRNA and sgRNA viral loads in nasal turbinates and wash of COH04S1-IM and COH04S1-IN-vaccinated animals appeared only marginally reduced, indicating limited vaccine impact on upper respiratory tract infection by COH04S1 independent of the vaccination route (Supplementary Fig. 2).
Histopathological findings in hematoxylin/eosin-stained lung sections of euthanized animals were assessed by a board-certified pathologist and scored in a blinded manner on a scale from 1 to 5 based on the severity and diffusion of the lesions (Supplementary Table 2). Control animals demonstrated compromised lung structure characterized by moderate bronchioloalveolar hyperplasia with consolidation of lung tissue, minimal to mild mononuclear or mixed cell inflammation, and syncytia formation (Fig. 2e–h). In contrast, COH04S1-IM-vaccinated animals did not show lung pathology of any type and grade in 6/6 hamsters, demonstrating potent vaccine protection against SARS-CoV-2-mediated lung injury in hamsters by IM vaccination with COH04S1. While COH04S1-IN-vaccinated animals presented no severe histopathological findings and significantly reduced lung pathology compared to controls, COH04S1-IN-vaccinated hamsters consistently showed a mild form of bronchioalveolar hyperplasia and grade 1 interstitial inflammation in a subset of animals, indicating that IN vaccination with COH04S1 mediated potent but incomplete vaccine protection against SARS-CoV-2-mediated lung damage in this model (Fig. 2e–h).
Correlative analysis of pre-challenge immunity and post-challenge outcome revealed that any of the evaluated COH04S1-induced responses, including S, RBD, and N-specific antibodies and NAb, correlated with protection from weight loss, lung infection, and lung pathology (Supplementary Fig. 3), confirming that the observed protection was vaccine-mediated. These results in sum demonstrate that hamsters vaccinated IM and IN with COH04S1 are protected from progressive weight loss, lower respiratory tract infection, and severe lung pathology following SARS-CoV-2 challenge.
2D and 1D vaccination of NHP with COH04S1 stimulates robust antigen-specific binding antibodies, NAb responses, and antigen-specific IFNγ and IL-2 expressing T cells
NHP represent a mild COVID-19 disease model that is widely used to bolster preclinical SARS-CoV-2 vaccine efficacy against upper and lower respiratory tract infection in an animal species that is more closely related to humans49,50,51,52,53,54,55,56. We used the African green monkey NHP model to assess COH04S1 vaccine protection against SARS-CoV-2 by 2D and 1D vaccination regimens, referred to as COH04S1-2D and COH04S1-1D, respectively. For 2D vaccination, NHP were vaccinated twice in a four-week interval with 2.5 × 108 PFU of COH04S1 by IM route. For 1D vaccination, NHP were vaccinated once with 5 × 108 PFU of COH04S1 by IM route (Fig. 3a). The choice for these specific doses was based on the rationale to evaluate the immunogenicity and efficacy of COH04S1 by 2D and 1D vaccination regimen that utilize in total the same amount of administered vaccine. As controls, NHP were either mock-vaccinated or vaccinated with empty sMVA vector via the same schedule and dose vaccination regimen. Robust serum binding antibodies to S, RBD, and N were stimulated in NHP by both COH04S1-2D and COH04S1-1D, whereas binding antibodies in the 2D vaccine group were strongly boosted after the second dose. At the time of challenge, S- and RBD-specific antibody titers measured in the 2D and 1D vaccine groups were comparable (Fig. 3b–d and Supplementary Fig. 4), while N-specific titers appeared higher in the 2D vaccine group than in the 1D vaccine group. Notably, high-titer S-specific antibody titers were measured in 2D- and 1D-vaccinated NHP by S antigens based on the original Wuhan-Hu-1 reference strain and various VOC (Beta, Gamma, Delta), indicating cross-reactivity of COH04S1-elicted NAb in NHP (Fig. 3e and Supplementary Fig. 4). Antigen-specific binding antibodies were also measured in lung bronchioalveolar lavage (BAL) samples two weeks pre-challenge. BAL IgG binding antibodies to S, RBD, and N were detected in both COH04S1-2D and COH04S1-1D-vaccinated NHP, although BAL IgG antibody titers measured at this time point pre-challenge were higher in the 2D vaccine group than in the 1D vaccine group (Fig. 3f and Supplementary Fig. 4).
NAb measurements based on PRNT assay revealed that both COH04S1-2D and COH04S1-1D elicited antibodies with efficacy to neutralize SARS-CoV-2 infectious virus (USA-WA1/2020). NAb responses measured in COH04S1-2D-vaccinated animals were boosted after the second dose and exceeded those measured in COH04S1-1D-vaccinated NHP at the time of challenge (Fig. 3g). Notably, NAb measured by PRNT assay in COH04S1-2D- and COH04S1-1D-vaccinated NHP were within the range of peak titers measured post-second dose in a cohort of healthcare workers that received the FDA-approved BNT162b2 mRNA vaccine from Pfizer/BioNTech. Attempts to assess VOC-specific NAb titers in COH04S1-vaccinated NHP using assays based on lentivirus and retrovirus-derived PV variants were inconclusive due to high unspecific background observed with samples of vaccinated and control animals. The precise reasons for these observations are unclear, although similar observations have been made for NHP by others57.
At two weeks pre-challenge, we also assessed SARS-CoV-2-specific T cells in COH04S1-vaccinated NHP. Both 2D and 1D vaccination with COH04S1 stimulated robust IFNγ and IL-2-expressing S and N antigen-specific T cells, whereas no or only very low levels of IL-4-expressing S- and N-specific T cells were observed in COH04S1-2D- or COH04S1-1D-vaccinated animals, consistent with Th1-biased immunity (Fig. 3h, i and Supplementary Fig. 5). S-specific T cells were generally detected at a higher frequency than N-specific T cells in both the COH04S1-2D and COH04S1-1D vaccine groups. In addition, S-specific T cells measured at this time point pre-challenge were detected at a higher frequency in 2D-vaccinated NHP than in 1D-vaccinated NHP. These results demonstrate that COH04S1 elicits robust antigen-specific binding antibodies, NAb, and antigen-specific IFNγ- and IL-2-expressing T cells in NHP through 2D and 1D vaccination regimens.
2D and 1D vaccination with COH04S1 protect NHP from lower and upper respiratory tract infection following SARS-CoV-2 challenge
Six weeks after 2D or 1D vaccination with COH04S1, NHP were challenged by IN/Intratracheal (IT) route with 1 × 105 PFU of SARS-CoV-2 (USA-WA1/2020). SARS-CoV-2 viral loads in lower and upper respiratory tracts were assessed at several time points for 21 days post challenge in BAL and nasal/oral swabs by quantification of gRNA and sgRNA and infectious virus titers (Figs. 4a–i and 5a–i and Supplementary Fig. 6). Progressively declining viral loads were overall measured over the 21 days post challenge observation period in BAL and nasal/oral swabs of both COH04S1-vaccinated NHP and control animals. Compared to BAL viral loads of control animals, markedly reduced gRNA and sgRNA copies and infectious virus titers were measured in BAL of COH04S1-2D and COH04S1-1D-vaccinated NHP at almost all time points post challenge (Figs. 4a, b, d, e, g, h), indicating a potent vaccine impact on lower respiratory tract infection. Notably, BAL gRNA and sgRNA copies and infectious titers measured in COH04S1-2D and COH04S1-1D-vaccinated NHP at day 2 immediately after challenge were on average 2–3 orders of magnitude lower than those measured in controls, confirming rapid vaccine efficacy. The marked reduction in BAL viral loads of COH04S1-vaccinated NHP compared to controls was confirmed when combining viral loads measured at all timepoints post challenge by area under the curve (AUC; Figs. 4c, f, i).
Similar to viral loads in BAL of COH04S1-vaccinated NHP, gRNA and sgRNA copies and infectious virus titers measured at the first 10 days post challenge in nasal swabs of COH04S1-2D or COH04S1-1D-vaccinated NHP were consistently lower than those of control animals, demonstrating vaccine efficacy to prevent upper respiratory tract infection (Fig. 5a–i). In addition, gRNA and sgRNA copies in oral swabs of COH04S1-vaccinated NHP tended to be consistently lower than those in oral swabs of control animals (Supplementary Fig. 6). Notably, nasal and oral swab gRNA and sgRNA copies and nasal swab infectious titers measured at 1–3 days immediately after challenge in COH04S1-vaccinated NHP were significantly reduced compared to those of controls, indicating immediate vaccine protection. Overall reduced nasal and oral swab viral loads in COH04S1-vaccinated NHP compared to control animals were confirmed when evaluating the nasal and oral swab viral loads over time by AUC (Figs. 5c, f, i and Supplementary Fig. 6). No significant differences in viral loads were observed between COH04S1-2D and COH04S1-1D-vaccinated animals, indicating similar protection against lower and upper respiratory tract infection by COH04S1 through 2D and 1D vaccination. Viral loads measured at day 7 or 21 post challenge in lung tissue and several other organs of necropsied animals did not indicate evident differences between COH04S1-vaccinated NHP and control animals (Supplementary Fig. 7). While gRNA and sgRNA copies measured at day 7 post challenge in lung samples of COH04S1-2D and COH04S1-1D-vaccinated NHP appeared reduced compared to those measured in lung samples of controls, these results were inconclusive due to low or undetectable gRNA and sgRNA levels in lung samples of the 1D mock-vaccinated control monkey (Supplementary Fig. 7). Histopathological findings assessed by a board-certified pathologist in a blinded manner at day 7 and 21 post challenge were generally only minor and comparable between COH04S1 vaccine and control groups, and no increase in inflammation was observed for COH04S1-vaccinated NHP compared to control animals (Supplementary Table 3). A strong inverse correlation could be assessed between vaccine-induced humoral and cellular immune responses, including S-, RBD-, and N-specific binding antibodies in serum and BAL, NAb, and S- and N-specific T cells, and SARS-CoV-2 viral loads in BAL and nasal swab samples (Supplementary Fig. 8). These results in sum demonstrate that 2D or 1D vaccination regimens of COH04S1 protect NHP from lower and upper respiratory tract infection following IN/IT challenge with SARS-CoV-2.
NHP vaccinated with 2D and 1D vaccination regimens of COH04S1 develop robust post-challenge anamnestic antiviral immune responses
To assess the vaccine impact on post-challenge viral immunity, humoral and cellular responses were evaluated in COH04S1-vaccinated NHP and control animals at 1, 2, and 3 weeks post-challenge (Fig. 6a–l and Supplementary Fig. 9). This analysis revealed that control animals developed robust binding antibodies to S, RBD, and N at 15- or 21-days post challenge (Fig. 6a–f), which indicated stimulation of potent humoral responses by the SARS-CoV-2 challenge virus in naïve NHP. In contrast, NAb titers measured post challenge in control animals by PRNT assay against infectious virus were in general relatively low or at the limit of detection (Figs. 6g, j), although elevated NAb responses were observed in 1D mock-vaccinated control animals at day 15 and 21 post challenge (Fig. 6j). In addition, no or only low level T cell responses were detected post-challenge in control animals, with the exception of elevated frequencies of S- and N-specific IFNγ-expressing T cell responses in mock-vaccinated control animals at day 7 post challenge (Figs. 6h, k, i, l).
Compared to antibodies measured pre-challenge in COH04S1-vaccinated NHP, boosted titers of S, RBD, and N antigen-specific binding antibodies and PRNT-assayed NAb were measured in COH04S1-vaccinated animals at day 15 and 21 post challenge (Figs. 6a–f, g, j), indicating induction of robust post-challenge anamnestic immune responses. This post-challenge booster effect on SARS-CoV-2-specific humoral immunity appeared more pronounced in COH04S1-1D-vaccinated NHP than in COH04S1-2D-vaccinated NHP, which may be a result of the lower pre-challenge responses in the 1D vaccine group compared to the 2D vaccine group. In addition, binding antibodies and NAb measured at day 15 and 21 post-challenge in COH04S1-vaccinated NHP generally exceeded those measured in control animals, indicating heightened vaccine-mediated humoral recall responses against SARS-CoV-2 through 2D or 1D vaccination. While S and N antigen-specific IFNγ-expressing T cell levels measured in COH04S1-2D-vaccinated animals tended to increase only slightly after challenge, a marked increase in post-challenge S- and N-specific IFNγ-expressing T cells was observed in COH04S1-1D-vaccinated NHP, indicating potent vaccine-mediated cellular recall responses following 1D vaccination (Figs. 6h, i, k, l). S- and N-specific IL-4-expressing T cells were either only very low or undetectable in COH04S1-vaccinated NHP and control animals at any time point post challenge, consistent with Th1-biased immunity following challenge (Supplementary Fig. 9). Correlation analysis did not unambiguously reveal a strong association between any of the post-challenge immunological parameters and post-challenge virological assessments (Supplementary Fig. 8). These results demonstrate that NHP vaccinated with 2D or 1D vaccination regimens of COH04S1 develop potent post-challenge anamnestic antiviral responses.
The emergence of several SARS-CoV-2 VOC with the capacity to evade S-specific NAb could possibly undermine the protective efficacy of approved COVID-19 vaccines, which utilize a single antigen design based solely on the S protein. One way to avoid or minimize the risk for SARS-CoV-2 evasion of vaccine-induced immunity could be the stimulation of broadly functional humoral and cellular immunity beyond the induction of S-specific NAb. Particularly the stimulation of T cells by a combination of multiple immunodominant antigens could act as an additional countermeasure to confer long-term and broadly effective immunity against SARS-CoV-2 and its emerging VOC21,22,23,24. Several recent studies indicate that SARS-CoV-2 VOC have the capacity to effectively escape humoral immunity, whereas they are less able to evade T cells elicited through natural infection and vaccination58.
Here, we demonstrate that multiantigenic sMVA-vectored SARS-CoV-2 vaccine COH04S1 co-expressing full-length S and N antigens provides potent immunogenicity and protective efficacy in animal models. We show in Syrian hamsters and NHP that COH04S1 elicits robust antigen-specific humoral and cellular immune responses and protects against SARS-CoV-2 challenge through different vaccination routes and dose regimens. A major limitation of the study is that we have not independently addressed the contribution of the S and N antigens to the observed protective efficacy of COH04S1 in these animal models as appropriate single antigen vectors were not evaluated. Nonetheless, the achieved primary goal of the study was to obtain preclinical evidence for the capacity of COH04S1 to induce protective immunity in suitable COVID-19 animal models. Despite these shortcomings, these positive results justify clinical evaluation of COH04S1 in ongoing (NCT046339466 and NCT04977024) and future clinical trials. COH04S1 represents a second-generation COVID-19 vaccine candidate that could be used alone or in combination with other existing vaccines in parenteral or mucosal prime-boost or single-shot vaccination strategies to augment vaccine-mediated protective immune responses against SARS-CoV-2.
Although several SARS-CoV-2 vaccines based on MVA have been developed and evaluated in animal models for immunogenicity and efficacy29,59,60,61,62, there is currently no MVA-based SARS-CoV-2 vaccine approved for routine clinical use. COH04S1 and MVA-SARS-2-S, an MVA vector expressing S alone, are currently the only MVA-based SARS-CoV-2 vaccines that are clinically evaluated62. In addition, COH04S1 and a recently developed adenovirus vector approach are currently the only clinically evaluated SARS-CoV-2 vaccines that utilize an antigen combination composed of S and N63. These findings highlight the potential importance of COH04S1 as a second generation multiantigenic SARS-CoV-2 vaccine to contribute to the establishment of long-term protective immunity to prevent COVID-19 disease. In addition, these findings highlight the potential of the sMVA platform and synthetic biology in poxvirus-vectored vaccine technology to rapidly generate protective and clinical-grade vaccine vectors for infectious disease prevention.
COH04S1 demonstrated potent immunogenicity in Syrian hamsters by IM and IN vaccination and in NHP by 2D and 1D vaccination regimens to elicit robust SARS-CoV-2-specific humoral and cellular immune responses to both S and N antigens. This included high-titer S- and N-specific binding antibodies in addition to robust binding antibodies targeting the RBD, the primary target of NAb. Binding antibodies elicited by COH04S1 in hamsters as well as T cell responses induced by COH04S1 in NHP indicated Th1-biased immunity, which is thought to be the preferred antiviral adaptive immune response to avoid vaccine-associated enhanced respiratory disease64,65. NAb elicited by COH04S1 in hamsters and NHP showed potent neutralizing activity against SARS-CoV-2 infectious virus, highlighting the potential of COH04S1 to induce antibody responses that are considered essential for protection against SARS-CoV-2. Notably, NAb titers stimulated by COH04S1 in NHP appeared similar to peak NAb titers stimulated in healthcare workers by two doses of the FDA approved Pfizer/BioNTech mRNA vaccine. In addition, NAb stimulated by COH04S1 in hamsters showed neutralizing activity against PV variants based on several SARS-CoV-2 VOC, including Alpha, Beta, Gamma, and the rapidly spreading Delta variant, indicating the capacity of COH04S1 to stimulate cross-protective NAb against SARS-CoV-2 VOC.
Both IM and IN vaccination with COH04S1 provided potent efficacy to protect Syrian hamsters from progressive weight loss, lower respiratory tract infection, and lung injury upon IN challenge with SARS-CoV-2, highlighting the potential of COH04S1 to stimulate protective immunity against SARS-CoV-2 respiratory infection through parenteral and mucosal vaccination routes. However, IM or IN vaccination of hamsters with COH04S1 appeared to provide only limited protection against upper respiratory tract infection, which was different from the marked reduction of nasal challenge virus loads in COH04S1-immunized NHP. This discrepancy in the observed levels of protection against upper respiratory tract infection afforded by COH04S1 in hamsters and NHP may have been result of the different time points that were analyzed to assess post challenge viral loads in these two animal models. Vaccinated NHP showed significantly reduced viral gRNA and sgRNA copies at days 1–2 post-challenge, while at day 10 post-challenge the reduction in viral loads of vaccinated NHP compared to controls did not reach significance. These findings for day 10 post-challenge viral loads in the NHP model appear to resemble the nasal viral loads that we have measured at day 10 post challenge in vaccinated hamsters, where only marginally reduced gRNA and sgRNA copies were observed when compared to controls. Consequently, day 10 post challenge may not have been an optimal time point to assess the vaccine impact on upper respiratory tract infection in the hamster model. Other reasons may also account for this apparent discrepancy observed in the two animal models, such as differences in the magnitude or quality of COH04S1 vaccine-elicited immune responses, susceptibility to SARS-CoV-2 infection, relative aggressiveness of viral challenge, or the time point of challenge after immunization.
The hamster weight loss analysis suggests that both IM and IN vaccination with COH04S1 mediated rapid disease control, while IN vaccination may provide superior protection compared to IM vaccination at the early phase after viral exposure. However, the precise levels of protection afforded by IN and IM vaccination with COH04S1 in hamsters at the early phase after challenge remain unclear, since viral loads were assessed only at day 10 post challenge, but not at day 2 or 4 immediately after virus exposure. On the other hand, hamsters vaccinated IM with COH041S1 were completely protected from lung injury following challenge, while hamsters vaccinated IN with COH04S1 showed minor lung pathology and inflammation at day 10 post challenge, suggesting superior protection against viral- or immune-mediated lung pathology through IM vaccination compared to IN vaccination with COH04S1. The precise reasons for the different pattern of protection through IN and IM immunization with COH04S1 in the Syrian hamster model remain unclear. It may be that IM and IN immunization of Syrian hamsters with COH04S1 induces qualitatively different systemic and mucosal humoral and cellular immune responses that provide altered levels of protection against SARS-CoV-2 infection in upper or lower respiratory tracts during early and late phases after virus challenge. Additional studies are needed to define the protection mediated by COH04S1 through IM and IN vaccination.
The immunogenicity and protective efficacy afforded by COH04S1 against SARS-CoV-2 in Syrian hamsters by IM and IN vaccination appears consistent with known properties of MVA-vectored vaccines. While MVA is well-known to stimulate robust immunity by IM vaccination, MVA has also been shown to elicit potent immunity through IN vaccination strategies at mucosal surfaces. A recombinant MVA vector expressing the S protein of Middle East Respiratory Syndrome coronavirus (MERS-CoV), a close relative of SARS-CoV-2, has recently been shown to be safe and immunogenic following IM administration in a Phase 1 clinical trial66. This MVA vaccine has also been shown to protect dromedary camels against MERS-CoV challenge by co-vaccination via IM and IN routes67. In addition, several animal studies have shown that IN vaccination with MVA vaccines is a potent stimulator of bronchus-associated lymphoid tissue, a tertiary lymphoid tissue structure within the lung that is frequently present in children and adolescents and that serves as a general priming site for T cells68. While the precise mechanism and levels of protection afforded by COH04S1 against SARS-CoV-2 in the Syrian hamster model by IM and IN vaccination remains unclear, especially at early phase after challenge, these findings support the use of COH04S1 to elicit SARS-CoV-2 protective immunity by mucosal vaccination.
In addition to the protection afforded by IM and IN vaccination with COH04S1 in hamsters, 2D and 1D vaccination with COH04S1 provided strong protection against lower and upper respiratory tract infection in NHP following IN/IT challenge with SARS-CoV-2. These findings demonstrate protective efficacy of COH04S1 by different dose vaccination regimens in a larger animal model that is thought to be critical to assess preclinical vaccine efficacy. Both 2D and 1D immunization with COH04S1 reduced SARS-CoV-2 viral loads in NHP immediately after challenge, indicating the capacity of COH04S1 to mediate rapid virus control upon exposure to SARS-CoV-2. Although post-challenge viral loads in BAL and nasal wash of vaccinated NHP were consistently lower than those of controls, this reduction in viral loads of vaccinated NHP compared to controls was only of significance at 1–2 days post challenge, which was likely associated with the limited group sizes and the large variation in viral loads between the animals in each group. While 2D and 1D vaccination of NHP with COH04S1 elicited similar S and RBD antigen-specific binding antibodies at the time of viral challenge, 2D vaccination appeared to be more effective than 1D vaccination in stimulating humoral and cellular responses, including NAb. Despite these lower pre-challenge immune responses in 1D-vaccinated animals compared to 2D-vaccinated NHP, 1D and 2D vaccination of NHP with COH04S1 afforded similar protection against lower and upper respiratory tract infection following viral challenge, suggesting that a single shot with COH04S1 is sufficient to induce protective immunity to SARS-CoV-2. These findings may also indicate that only relatively low levels of vaccine-induced humoral and cellular immune responses are required to effectively control SARS-CoV-2 infection in this model. In addition, while 2D vaccination with COH04S1 appeared to elicit more potent pre-challenge responses than 1D vaccination, overall more potent post-challenge anamnestic antiviral immune responses were observed in 1D-vaccinated NHP compared to 2D-vaccinated NHP, suggesting that a single shot with COH04S1 is sufficient to effectively prime vaccine-mediated protective recall responses to SARS-CoV-2. Whether the protection afforded by COH04S1 in NHP through 2D and 1D vaccination regimens is primarily mediated by NAb or complemented by a combination of multiple S and N antigen-specific humoral and cellular effector functions remains to be determined in future studies10.
How COH04S1 compares to clinically approved COVID-19 vaccines for efficacy to protect against upper and lower respiratory tract infection in NHP and how these preclinical vaccine assessments may translate into clinical effectiveness is difficult to assess. Unlike the dual antigen design of COH04S1 that is based on co-expression of full-length, unmodified S and N antigens sequences, the mRNA vaccines mRNA-1273 (EUA) and BNT162b2 (FDA approved) and the Ad26.COV2.S adenovirus vaccine (EUA) use a single antigen design based on a prefusion stabilized S protein52,53,69, which can improve vaccine immunogenicity and efficacy as demonstrated for Ad26.COV2.S69. The use of unmodified antigen sequences for COH04S1 was mainly based on the rationale to express S and N antigens that reflect native protein forms of SARS-CoV-2. COH04S1 afforded potent immune function to control SARS-CoV-2 infection at both upper and lower respiratory tracts in NHP, with some animals demonstrating complete protection of the lower respiratory tract. However, in most COH04S1-vaccinated NHP the protective efficacy was incomplete as progressively declining viral genome copies were measured following challenge in BAL and nasal samples over an extended period of time. This appears to be different from the complete or near-complete protection of upper and lower respiratory tracts observed with the mRNA or Ad26 vaccines in NHP, where viral genomes were either undetectable or only detectable at very low levels at single time points in BAL and nasal samples of most of the vaccinated NHP52,53,69. Most impressive are the findings for the Ad26 vaccine that demonstrated efficacy to suppress viral replication almost completely in both upper and lower respiratory tracts through singe-dose immunization69. These observations may suggest that COH04S1 is less effective compared to the mRNA or Ad26 vaccines to provide protection against SARS-CoV-2. However, the protection studies with COH04S1 and EUA COVID-19 vaccines in NHP are difficult to compare due to differences in the experimental setup and the use of different primate models that may have resulted in variable levels of infection and viral loads. While the mRNA and Ad26 vaccines were evaluated in outbred rhesus macaques, we investigated the protective efficacy of COH04S1 in wild-caught African green monkeys. It appears that the viral loads that we observed in the COH04S1 efficacy study in African green monkeys were much higher in vaccinated and control animals than those reported for the mRNA and Ad26 vaccine studies in rhesus macaques52,53,69, particularly when compared to the mRNA vaccine studies52,53. These findings are in line with previous studies in NHP infected with SARS and SARS-CoV-2 that describe African green monkeys as the NHP model supporting the highest level of viral replication with sustained replication in the lower respiratory tract49,70. These findings may suggest that the protective function of COH04S1 in NHP was evaluated under more stringent or aggressive conditions compared to the protection studies with the mRNA and Ad26 vaccines in NHP. How these findings translate into clinical efficacy is difficult to determine, but the fact that COH04S1 provides potent protective efficacy in two different animal models that are considered important to assess preclinical COVID-19 vaccine efficacy may be indicative of the capacity of COH04S1 to elicit protective immunity against SARS-CoV-2 in humans. COH04S1 likely confers protection through different immune mechanisms than the mRNA and Ad26 vaccines and may therefore be particularly valuable as a complementary booster shot to augment the quality of SARS-CoV-2 protective immune responses conferred by EUA or FDA-approved COVID-19 vaccines.
These results in sum demonstrate that COH04S1 has the capacity to elicit potent and cross-reactive Th1-biased S- and N-specific humoral and cellular responses that protect hamsters and NHP from SARS-CoV-2 by different vaccination routes and dose regimens. This multi-antigen sMVA-vectored SARS-CoV-2 vaccine could be complementary to available vaccines to induce robust and long-lasting protective immunity against SARS-CoV-2 and its emerging VOC.
COH04S1 and sMVA vaccine vectors
COH04S1 is a double-plaque purified virus isolate derived from the previously described sMVA-N/S vector (NCBI Accession# MW036243), which was generated using the three-plasmid system of the sMVA platform and fowlpox virus TROVAC as a helper virus for virus reconstitution29. COH04S1 co-expresses full-length, unmodified S and N antigen sequences based on the Wuhan-Hu-1 reference strain (NCBI Accession# NC_045512)29. Sequence identity of COH04S1 seed stock virus was assessed by PaqBio long-read sequencing. COH04S1 and sMVA vaccine stocks for animal studies were produced using chicken embryo fibroblasts (CEF) and prepared by 36% sucrose cushion ultracentrifugation and virus resuspension in 1 mM Tris-HCl (pH 9). Virus stocks were stored at −80 °C and titrated on CEF by plaque immunostaining as described29. Viral stocks were validated for antigen insertion and expression by PCR, sequencing, and Immunoblot.
Animals, study design and challenge
In life portion of hamsters and NHP studies were carried out at Bioqual Inc. (Rockville, MD). Thirty 6–8 weeks old Syrian hamsters were randomly assigned to the groups, with 3 females and 3 males in each group. Hamsters were IM or IN vaccinated four weeks apart with 1 × 108 PFU of COH04S1 or sMVA vaccine stocks diluted in phosphate-buffered saline (PBS). Two weeks post-booster vaccination, animals were challenged IN (50 µl/nare) with 3 × 104 PFU (or 1.99 × 104 Median Tissue Culture Infectious Dose, [TCID50]) of SARS-CoV-2 USA-WA1/2020 (BEI Resources; P4 animal challenge stock, NR-53780 lot no. 70038893). The stock was produced by infecting Vero E6-hACE2 cells (BEI Resources NR-53726) at low MOI with deposited passage 3 virus and resulted in a titer of 1.99 × 106 TCID50/ml. Sequence identity was confirmed by next generation sequencing. Body weight was recorded daily for 10 days. Hamsters were humanely euthanized for lung samples collection. A total of 24 African green monkeys (Chlorocebus aethiops; 20 females and 4 males) from St. Kitts weighting 3–6 kg were randomized by weight and sex to vaccine and control groups. For 2D vaccination, NHP were vaccinated twice four weeks apart with 2.5 × 108 PFU of COH04S1 (n = 6) or sMVA control vector (n = 3) diluted in PBS. For 1D vaccination, NHP were vaccinated once with 5 × 108 PFU of COH04S1 (n = 6) or sMVA control vector (n = 3) diluted in PBS. Mock-vaccinated NHP immunized once (n = 3) or twice (n = 3) with PBS only were used as additional controls. At six weeks post vaccination, NHP were challenged with 1 × 105 TCID50 of SARS-CoV-2 USA-WA1/2020 strain diluted in PBS via combined IT (1 ml)/IN (0.5 ml/nare) route. Necropsy was performed 7 days and 21 days following challenge and organs were collected for gross pathology and histopathology. All animal studies were conducted in compliance with local, state, and federal regulations and were approved by Bioqual and City of Hope Institutional Animal Care and Use Committees (IACUC).
ELISA binding antibody detection
SARS-CoV-2-specific binding antibodies in hamster and NHP samples were detected by indirect ELISA using purified S, RBD, and N proteins (Sino Biological 40589-V08B1, 40592-V08H, 40588-V08B), or Beta, Gamma, and Delta VOC-specific S proteins (Acro Biosystems SPN-C52Hk, SPN-C52Hg, SPN-C52He). 96-well plates were coated with 100 μl/well of S, RBD, or N protein at a concentration of 1 μg/ml in PBS and incubated overnight at 4 oC. For binding antibody detection in hamsters serum, plates were washed 5X with wash buffer (0.05% Tween-20/PBS), then blocked with 250 μl/well of blocking buffer (0.5% casein/154 mM NaCl/10 mM Tris-HCl [pH 7.6]) for 2 h at room temperature. After washing, 3-fold diluted heat-inactivated serum in blocking buffer was added to the plates and incubated 2 h at room temperature. After washing, anti-Hamster IgG HRP secondary antibodies measuring total IgG(H + L), IgG1, or IgG2/IgG3 (Southern Biotech 6061-05, 1940-05, 1935-05) were diluted 1:1000 in blocking buffer and added to the plates. After 1 h incubation, plates were washed and developed with 1 Step TMB-Ultra (Thermo Fisher 34029). The reaction was stopped with 1 M H2SO4 and plates were immediately read on FilterMax F3 (Molecular Devices). For binding antibody detection in NHP serum, a similar protocol was used. Wash buffer was 0.1% Tween-20/PBS, and blocking buffer was 1% casein/PBS for RBD and N antigen ELISA and 4% Normal Goat Serum/1% casein/PBS for S antigen ELISA. For IgG quantification in NHP BAL samples 1% BSA/PBS was used as blocking and sample buffers. Goat anti-Monkey IgG (H + L) secondary antibody (ThermoFisher PA1-84631) was diluted 1:10,000. Endpoint titers were calculated as the highest dilution to have an absorbance >0.100 nm.
NAb were measured by PRNT assay using SARS-CoV-2 USA-WA1/2020 strain (Lot # 080420-900). The stock was generated using Vero-E6 cells infected with seed stock virus obtained from Kenneth Plante at UTMB (lot # TVP 23156). Vero E6 cells (ATCC, CRL-1586) were seeded in 24-well plates at 175,000 cells/well in DMEM/10% FBS/Gentamicin. Serial 3-fold serum dilutions were incubated in 96-well plates with 30 PFU of SARS-CoV-2 USA-WA1/2020 strain for 1 h at 37 °C. The serum/virus mixture was transferred to Vero-E6 cells and incubated for 1 h at 37 °C. After that, 1 ml of 0.5% methylcellulose media was added to each well, and plates were incubated at 37 °C for three days. Plates were washed, and cells were fixed with methanol. Crystal violet staining was performed, and plaques were recorded. IC50 titers were calculated as the serum dilution that gave a 50% reduction in viral plaques in comparison to control wells. Serum samples collected from City of Hope healthcare workers (N = 14) at day 60 post Pfizer/BioNTech BNT162b2 mRNA vaccination were part of an IRB-approved observational study to establish durability of immunogenic properties of EUA vaccines against COVID-19 (IRB20720). Subjects gave informed consent.
SARS-CoV-2 PV was produced using a plasmid lentiviral system based on pALD-gag-pol, pALD-rev, and pALD-GFP (Aldevron). Plasmid pALD-GFP was modified to express Firefly luciferase (pALD-Fluc). Plasmid pCMV3-S (Sino Biological VG40589-UT) was used and modified to express SARS-CoV-2 Wuhan-Hu-1 S with D614G modification. Customized gene sequences cloned into pTwist-CMV-BetaGlobin (Twist Biosciences) were used to express SARS-CoV-2 VOC-specific S variants (Supplementary Table 1). All S antigens were expressed with C-terminal 19aa deletion. A transfection mixture was prepared 1 ml OptiMEM that contained 30 µl of TransIT-Lenti transfection reagent (Mirus MIR6600) and 6 µg pALD-Fluc, 6 µg pALD-gag-pol, 2.4 µg pALD-rev, and 6.6 µg S expression plasmid. The mixture was added to 5 × 106 HEK293T/17 cells (ATCC CRL11268) seeded the day before in 10 cm dishes and the cells were incubated for 72 h at 37 °C. Supernatant containing PV was harvested and frozen in aliquots at −80 °C. Lentivirus was titrated using the Lenti-XTM p24 Rapid Titer Kit (Takara) according to the manufacturer’s instructions.
Pseudovirus neutralization assay
SARS-CoV-2 PV was titrated in vitro to calculate the virus stock amount that equals 100,000–200,000 relative luciferase units. Flat-bottom 96-well plates were coated with 100 μL poly-L-lysine (0.01%). Serial 2-fold serum dilutions starting from 1:20 were prepared in 50 μL media and added to the plates in triplicates, followed by 50 μL of PV. Plates were incubated overnight at 4 °C. The following day, 10,000 HEK293T-ACE2 cells71 were added to each well in the presence of 3 µg/ml polybrene and plates were incubated at 37 °C. After 48 h of incubation, luciferase lysis buffer (Promega E1531) was added, and luminescence was quantified using SpectraMax L (Molecular Devices) after adding 100 μL Luciferase Assay Reagent (Promega E1483) luciferin/well and using 10 s integration time. For each plate, positive (PV only) and negative (cells only) controls were added in triplicate. The neutralization titer for each dilution was calculated as follows: NT = [1 − (mean luminescence with immune sera / mean luminescence without immune sera)] × 100. The titers that gave 50% neutralization (NT50) were calculated by determining the linear slope of the graph plotting NT versus serum dilution by using the next higher and lower NT using Office Excel (v2019).
ELISPOT T cell detection
Peripheral blood mononuclear cells (PBMC) were isolated from fresh blood using Ficoll and counted using Luna-FL cell counter (Logos Biosystems). Pre-immune samples were evaluated using Human IFN-γ/IL-4 Double-Color FluoroSpot (ImmunoSpot); however, this kit only allowed to assess NHP IFN-γ but not NHP IL-4. The remaining time-points were evaluated using Monkey IFNγ/IL-4 FluoroSpot FLEX kit and Monkey IL-2 FluoroSpot FLEX kit (Mabtech, X-21A16B and X-22B) following manufacturer instructions. Briefly, 200,000 cells/well in CTL-test serum free media (Immunospot CTLT-010) were added to duplicate wells and stimulated with peptide pools (15-mers, 11 aa overlap, >70% purity). Spike peptide library (GenScript) consisted of 316 peptides and was divided into 4 sub-pools spanning the S1 and S2 domains (1S1 = 1–86; 1S2 = 87–168; 2S1 = 169–242; 2S2 = 243–316; peptides 173 and 304–309 were not successfully synthesized and were therefore excluded from the pools). Nucleocapsid (GenScript) and Membrane (in house synthesized) libraries consisted of 102 and 53 peptides, respectively. Each peptide pool (2 µg/ml) and αCD28 (0.1 µg/ml, Mabtech) were added to the cells and plates were incubated for 48 h at 37 °C. Control cells (25,000/well) were stimulated with PHA (10 µg/ml). After incubation, plates were washed, and primary and secondary antibodies were added according to manufacturer’s protocol. Fluorescent spots were acquired using CTL S6 Fluorocore (Immunospot). For each sample, spots in unstimulated DMSO-only control wells were subtracted from spots in stimulated wells. Total spike response was calculated as the sum of the response to each spike sub-pool.
SARS-CoV-2 gRNA copies per ml nasal wash, BAL fluid or swab, or per gram of tissue were quantified by qRT-PCR assay (Bioqual, SOP BV-034) using primer/probe sequences binding to a conserved region of SARS-CoV-2 N gene. Viral RNA was isolated from BAL fluid or swabs using the Qiagen MinElute virus spin kit (57704). For tissues, viral RNA was extracted with RNA-STAT 60 (Tel-test B)/chloroform, precipitated and resuspended in RNAse-free water. To generate a control for the amplification, RNA was isolated from SARS-CoV-2 virus stocks. RNA copies were determined from an O.D. reading at 260, using the estimate that 1.0 OD at A260 equals 40 µg/ml of RNA. A final dilution of 108 copies per 3 µl was then divided into single use aliquots of 10 µl. These were stored at −80 oC until needed. For the master mix preparation, 2.5 ml of 2X buffer containing Taq-polymerase, obtained from the TaqMan RT-PCR kit (Bioline BIO-78005), was added to a 15 ml tube. From the kit, 50 µl of the RT and 100 µl of RNAse inhibitor were also added. The primer pair at 2 µM concentration was then added in a volume of 1.5 ml. Last, 0.5 ml of water and 350 µl of the probe at a concentration of 2 µM were added and the tube vortexed. For the reactions, 45 µl of the master mix and 5 µl of the sample RNA were added to the wells of a 96-well plate. All samples were tested in triplicate. The control RNA was prepared to contain 106 to 107 copies per 3 µl. Eight 10-fold serial dilutions of control RNA were prepared using RNAse-free water by adding 5 µl of the control to 45 µl of water. Duplicate samples of each dilution were prepared as described. PCR amplification was performed in an Applied Biosystems 7500 Sequence detector using the following program: 48 oC for 30 min, 95 oC for 10 min followed by 40 cycles of 95 oC for 15 sec, and 1 min at 55 oC. The number of copies of RNA per ml was calculated by extrapolation from the standard curve and multiplying by the reciprocal of 0.2 ml extraction volume. This gave a practical range of 50 to 5 × 108 RNA copies per swabs or per ml BAL fluid. Primer/probe sequences: 5′-GAC CCC AAA ATC AGC GAA AT-3′; 5′-TCT GGT TAC TGC CAG TTG AAT CTG-3′; and 5′-FAM-ACC CCG CAT TAC GTT TGG TGG ACC-BHQ1-3′.
SARS-CoV-2 sgRNA copies were assessed through quantification of N gene mRNA by qRT-PCR using primer/probe sequences that were specifically designed to amplify and bind to a region of the N gene mRNA that is not packaged into virions. SARS-CoV-2 RNA was extracted from samples as described above. The signal was compared to a known standard curve of plasmid containing a cDNA copy of the N gene mRNA target region to give copies per ml. PCR amplification was performed in an Applied Biosystems 7500 Sequence detector using the following program: 48 °C for 30 min, 95 °C for 10 min followed by 40 cycles of 95 °C for 15 sec, and 1 min at 55 °C. The number of copies of RNA per ml was calculated by extrapolation from the standard curve and multiplying by the reciprocal of 0.2 ml extraction volume. This gave a practical range of 50 to 5 × 107 RNA copies per swab or ml BAL fluid. Primer/probe sequences: 5′-CGA TCT CTT GTA GAT CTG TTC TC-3′; 5′-GGT GAA CCA AGA CGC AGT AT-3′; 5′-FAM- TAA CCA GAA TGG AGA ACG CAG TGG G-BHQ-3′.
Infectious titer quantification
Vero TMPRSS2 cells (Vaccine Research Center-NIAID) were plated at 25,000 cells/well in DMEM/10% FBS/Gentamicin. Ten-fold dilutions of the sample starting from 20 μl of material were added to the cells in quadruplicates and incubated at 37 °C for 4 days. The cell monolayers were visually inspected, and presence of CPE noted. TCID50 values were calculated using the Read-Muench formula.
Histopathological evaluation of hamsters and NHP lung sections were performed by Experimental Pathology Laboratories, Inc. (Sterling, VA) and Charles River (Wilmington, MA), respectively. At necropsy organs were collected and placed in 10% neutral buffered formalin for histopathologic analysis. Tissues were processed through to paraffin blocks, sectioned once at ~5 μm thickness, and stained with hematoxylin/eosin. Board certified pathologists were blinded to the vaccine groups and mock controls were used as a comparator.
Statistical analyses were performed using Prism 8 (GraphPad, v8.3.0). One-way ANOVA with Holm-Sidak’s multiple comparison test, two-way ANOVA with Tukey’s or Dunn’s multiple comparison test, Kruskal–Wallis test followed by Dunn’s multiple comparison test, and Spearman correlation analysis were used. All tests were two-sided. The test applied for each analysis and the significance level is indicated in each figure legend. Prism 8 was used to derive correlation matrices.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
All relevant data of this study are available from the corresponding authors upon request.
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We would like to thank Angela Wong and Christina Ulloa for helping with laboratory logistics and secretarial support. We would like to acknowledge the Bioqual team for their technical support. We gratefully acknowledge City of Hope’s unique internal funding mechanism of selected scientific discoveries, enabling preclinical and clinical development to speedily advance products toward commercialization, such as COH04S1. The following reagent was deposited by the Centers for Disease Control and Prevention and obtained through BEI Resources, NIAID, NIH: SARS-Related Coronavirus 2, Isolate USA-WA1/2020, NR-53780. D.J.D. was partially supported by the following Public Health Service grants: U19 AI128913, CA111412, CA181045, and CA107399. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Funds were allocated to D.J.D. by the City of Hope (COH) for research that resulted in the development of COH04S1, the multi-antigenic SARS-CoV-2 vaccine using a synthetic poxvirus platform that is discussed in this publication. While unknown whether publication of this report will aid in receiving grants and contracts, it is possible that this publication will be of benefit to COH. COH had no role in the conceptualization, design, data collection, analysis, decision to publish, or preparation of the manuscript. COH submitted two PCT applications. D.J.D. is a co-inventor on two patent applications that were submitted by COH to the USPTO. One patent application (PCT/US2021/016247) covers the design and construction of the synthetic MVA platform, and another patent application (PCT/US2021/032821) covers the development of a COVID-19 vaccine. F.W. is a co-inventor of the same two PCT applications that apply to D.J.D. F.C. is a co-inventor of the PCT application that covers the development of a COVID-19 vaccine. All remaining authors that have not been referenced above have no competing interests as defined by Nature Research, or other interests that might be perceived to influence the interpretation of the article.
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Chiuppesi, F., Nguyen, V.H., Park, Y. et al. Synthetic multiantigen MVA vaccine COH04S1 protects against SARS-CoV-2 in Syrian hamsters and non-human primates. npj Vaccines 7, 7 (2022). https://doi.org/10.1038/s41541-022-00436-6