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

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...

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Autores principales: Akache, Bassel, Renner, Tyler M., Stuible, Matthew, Rohani, Nazanin, Cepero-Donates, Yuneivy, Deschatelets, Lise, Dudani, Renu, Harrison, Blair A., Gervais, Christian, Hill, Jennifer J., Hemraz, Usha D., Lam, Edmond, Régnier, Sophie, Lenferink, Anne E. G., Durocher, Yves, McCluskie, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9555707/
https://www.ncbi.nlm.nih.gov/pubmed/36224247
http://dx.doi.org/10.1038/s41541-022-00540-7
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author Akache, Bassel
Renner, Tyler M.
Stuible, Matthew
Rohani, Nazanin
Cepero-Donates, Yuneivy
Deschatelets, Lise
Dudani, Renu
Harrison, Blair A.
Gervais, Christian
Hill, Jennifer J.
Hemraz, Usha D.
Lam, Edmond
Régnier, Sophie
Lenferink, Anne E. G.
Durocher, Yves
McCluskie, Michael J.
author_facet Akache, Bassel
Renner, Tyler M.
Stuible, Matthew
Rohani, Nazanin
Cepero-Donates, Yuneivy
Deschatelets, Lise
Dudani, Renu
Harrison, Blair A.
Gervais, Christian
Hill, Jennifer J.
Hemraz, Usha D.
Lam, Edmond
Régnier, Sophie
Lenferink, Anne E. G.
Durocher, Yves
McCluskie, Michael J.
author_sort Akache, Bassel
collection PubMed
description 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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spelling pubmed-95557072022-10-13 Immunogenicity of SARS-CoV-2 spike antigens derived from Beta & Delta variants of concern Akache, Bassel Renner, Tyler M. Stuible, Matthew Rohani, Nazanin Cepero-Donates, Yuneivy Deschatelets, Lise Dudani, Renu Harrison, Blair A. Gervais, Christian Hill, Jennifer J. Hemraz, Usha D. Lam, Edmond Régnier, Sophie Lenferink, Anne E. G. Durocher, Yves McCluskie, Michael J. NPJ Vaccines Brief Communication 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. Nature Publishing Group UK 2022-10-12 /pmc/articles/PMC9555707/ /pubmed/36224247 http://dx.doi.org/10.1038/s41541-022-00540-7 Text en © Crown 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Brief Communication
Akache, Bassel
Renner, Tyler M.
Stuible, Matthew
Rohani, Nazanin
Cepero-Donates, Yuneivy
Deschatelets, Lise
Dudani, Renu
Harrison, Blair A.
Gervais, Christian
Hill, Jennifer J.
Hemraz, Usha D.
Lam, Edmond
Régnier, Sophie
Lenferink, Anne E. G.
Durocher, Yves
McCluskie, Michael J.
Immunogenicity of SARS-CoV-2 spike antigens derived from Beta & Delta variants of concern
title Immunogenicity of SARS-CoV-2 spike antigens derived from Beta & Delta variants of concern
title_full Immunogenicity of SARS-CoV-2 spike antigens derived from Beta & Delta variants of concern
title_fullStr Immunogenicity of SARS-CoV-2 spike antigens derived from Beta & Delta variants of concern
title_full_unstemmed Immunogenicity of SARS-CoV-2 spike antigens derived from Beta & Delta variants of concern
title_short Immunogenicity of SARS-CoV-2 spike antigens derived from Beta & Delta variants of concern
title_sort immunogenicity of sars-cov-2 spike antigens derived from beta & delta variants of concern
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9555707/
https://www.ncbi.nlm.nih.gov/pubmed/36224247
http://dx.doi.org/10.1038/s41541-022-00540-7
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