Immunogenicity of SARS-CoV-2 spike antigens derived from Beta & Delta variants of concern

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作者
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
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[1] Human Health Therapeutics,National Research Council Canada
[2] Human Health Therapeutics,National Research Council Canada
[3] National Research Council Canada,undefined
[4] Aquatic and Crop Resource Development,undefined
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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.
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