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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-9555707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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