Efficacy of a stable broadly protective subunit vaccine platform against SARS-CoV-2 variants of concern
dc.contributor.author | Garg, Ravendra | |
dc.contributor.author | Liu, Qiang | |
dc.contributor.author | Kessel, Jill Van | |
dc.contributor.author | Asavajaru, Akarin | |
dc.contributor.author | Uhlemann, Eva-Maria | |
dc.contributor.author | Joessel, Morgane | |
dc.contributor.author | Hamonic, Glenn | |
dc.contributor.author | khatooni, zahed | |
dc.contributor.author | Kroeker, Andrea | |
dc.contributor.author | Lew, Jocelyne | |
dc.contributor.author | Scruten, Erin | |
dc.contributor.author | Pennington, Paul | |
dc.contributor.author | Deck, William | |
dc.contributor.author | Prysliak, Tracy | |
dc.contributor.author | Nickol, Michaela | |
dc.contributor.author | Apel, Falko | |
dc.contributor.author | Courant, Thomas | |
dc.contributor.author | Kelvin, Alyson A. | |
dc.contributor.author | Kessel, Andrew Van | |
dc.contributor.author | Collin, Nicolas | |
dc.contributor.author | Gerdts, Volker | |
dc.contributor.author | Köster, Wolfgang | |
dc.contributor.author | Falzarano, Darryl | |
dc.contributor.author | Racine, Trina | |
dc.contributor.author | Banerjee, Arinjay | |
dc.date.accessioned | 2025-05-09T17:44:00Z | |
dc.date.available | 2025-05-09T17:44:00Z | |
dc.date.issued | 2024-05 | |
dc.description.abstract | The emergence and ongoing evolution of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has highlighted the need for rapid vaccine development platforms that can be updated to counteract emerging variants of currently circulating and future emerging coronaviruses. Here we report the development of a “train model” subunit vaccine platform that contains a SARS-CoV-2 Wuhan S1 protein (the “engine”) linked to a series of flexible receptor binding domains (RBDs; the “cars”) derived from SARS-CoV-2 variants of concern (VOCs). We demonstrate that these linked subunit vaccines when combined with Sepivac SWE™, a squalene in water emulsion (SWE) adjuvant, are immunogenic in Syrian hamsters and subsequently provide protection from infection with SARS-CoV-2 VOCs Omicron (BA.1), Delta, and Beta. Importantly, the bivalent and trivalent vaccine candidates offered protection against some heterologous SARS-CoV-2 VOCs that were not included in the vaccine design, demonstrating the potential for broad protection against a range of different VOCs. Furthermore, these formulated vaccine candidates were stable at 2–8 °C for up to 13 months post-formulation, highlighting their utility in low-resource settings. Indeed, our vaccine platform will enable the development of safe and broadly protective vaccines against emerging betacoronaviruses that pose a significant health risk for humans and agricultural animals. | |
dc.description.sponsorship | This study was funded by a grant from the Coalition for Epidemic Preparedness Innovations (CEPI). D.F. acknowledges funding from the Canadian Institutes of Health Research (PJT – 153319; VS1-175531). A.B. acknowledges funding from the Canadian Institutes of Health Research (CIHR)-Centre for Research on Pandemic Preparedness and Health Emergencies, Early Career Investigator Grant (FRN: PEE-183995). The authors would also like to thank the Vaccine Formulation Institute (VFI) for their collaboration and VIDO’s veterinary staff for their tremendous efforts. VIDO receives operational funding from the Canada Foundation for Innovation through the Major Science Initiatives, from the Government of Saskatchewan through Innovation Saskatchewan, and the Ministry of Agriculture. Some figures were generated using BioRender.com. | |
dc.description.version | Peer Reviewed | |
dc.identifier.citation | Garg, R., Liu, Q., Van Kessel, J., Asavajaru, A., Uhlemann, E.-M., Joessel, M., Hamonic, G., Khatooni, Z., Kroeker, A., Lew, J., Scruten, E., Pennington, P., Deck, W., Prysliak, T., Nickol, M., Apel, F., Courant, T., Kelvin, A. A., Van Kessel, A., … Banerjee, A. (2024). Efficacy of a stable broadly protective subunit vaccine platform against SARS-CoV-2 variants of concern. Vaccine, 42(20), 125980–125980. https://doi.org/10.1016/j.vaccine.2024.05.028 | |
dc.identifier.doi | https://doi.org/10.1016/j.vaccine.2024.05.028 | |
dc.identifier.uri | https://hdl.handle.net/10388/16924 | |
dc.language.iso | en | |
dc.publisher | ScienceDirect | |
dc.rights | Attribution 2.5 Canada | en |
dc.rights.uri | http://creativecommons.org/licenses/by/2.5/ca/ | |
dc.subject | SARS-CoV-2 | |
dc.subject | betacoronaviruses | |
dc.subject | agricultural animals | |
dc.title | Efficacy of a stable broadly protective subunit vaccine platform against SARS-CoV-2 variants of concern | |
dc.type | Article |