npj Vaccines
(Oct 2022)
Immunogenicity of SARS-CoV-2 spike antigens derived from Beta & Delta variants of concern
Bassel Akache,
Tyler M. Renner,
Matthew Stuible,
Nazanin Rohani,
Yuneivy Cepero-Donates,
Lise Deschatelets,
Renu Dudani,
Blair A. Harrison,
Christian Gervais,
Jennifer J. Hill,
Usha D. Hemraz,
Edmond Lam,
Sophie Régnier,
Anne E. G. Lenferink,
Yves Durocher,
Michael J. McCluskie
Affiliations
Bassel Akache
National Research Council Canada, Human Health Therapeutics
Tyler M. Renner
National Research Council Canada, Human Health Therapeutics
Matthew Stuible
National Research Council Canada, Human Health Therapeutics
Nazanin Rohani
National Research Council Canada, Human Health Therapeutics
Yuneivy Cepero-Donates
National Research Council Canada, Human Health Therapeutics
Lise Deschatelets
National Research Council Canada, Human Health Therapeutics
Renu Dudani
National Research Council Canada, Human Health Therapeutics
Blair A. Harrison
National Research Council Canada, Human Health Therapeutics
Christian Gervais
National Research Council Canada, Human Health Therapeutics
Jennifer J. Hill
National Research Council Canada, Human Health Therapeutics
Usha D. Hemraz
National Research Council Canada, Aquatic and Crop Resource Development
Edmond Lam
National Research Council Canada, Aquatic and Crop Resource Development
Sophie Régnier
National Research Council Canada, Aquatic and Crop Resource Development
Anne E. G. Lenferink
National Research Council Canada, Human Health Therapeutics
Yves Durocher
National Research Council Canada, Human Health Therapeutics
Michael J. McCluskie
National Research Council Canada, Human Health Therapeutics
DOI
https://doi.org/10.1038/s41541-022-00540-7
Journal volume & issue
Vol. 7,
no. 1
pp.
1
– 7
Abstract
Read online
Abstract Using our strongly immunogenic SmT1 SARS-CoV-2 spike antigen platform, we developed antigens based on the Beta & Delta variants of concern (VOC). These antigens elicited higher neutralizing antibody activity to the corresponding variant than comparable vaccine formulations based on the original reference strain, while a multivalent vaccine generated cross-neutralizing activity in all three variants. This suggests that while current vaccines may be effective at reducing severe disease to existing VOC, variant-specific antigens, whether in a mono- or multivalent vaccine, may be required to induce optimal immune responses and reduce infection against arising variants.
Published in npj Vaccines
ISSN
2059-0105 (Online)
Publisher
Nature Portfolio
Country of publisher
United Kingdom
LCC subjects
Medicine: Internal medicine: Specialties of internal medicine: Immunologic diseases. Allergy
Medicine: Internal medicine: Neoplasms. Tumors. Oncology. Including cancer and carcinogens
Website
https://www.nature.com/npjvaccines/
About the journal
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