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Omicron BA.1 and BA.2 neutralizing activity elicited by a comprehensive panel of human vaccines
The SARS-CoV-2 Omicron variant of concern comprises three sublineages designated BA.1, BA.2, and BA.3, with BA.2 steadily replacing the globally dominant BA.1. We show that the large number of BA.1 and BA.2 spike mutations severely dampen plasma neutralizing activity elicited by infection or seven c...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Cold Spring Harbor Laboratory
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8936098/ https://www.ncbi.nlm.nih.gov/pubmed/35313570 http://dx.doi.org/10.1101/2022.03.15.484542 |
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author | Bowen, John E. Sprouse, Kaitlin R. Walls, Alexandra C. Mazzitelli, Ignacio G. Logue, Jennifer K. Franko, Nicholas M. Ahmed, Kumail Shariq, Asefa Cameroni, Elisabetta Gori, Andrea Bandera, Alessandra Posavad, Christine M. Dan, Jennifer M. Zhang, Zeli Weiskopf, Daniela Sette, Alessandro Crotty, Shane Iqbal, Najeeha Talat Corti, Davide Geffner, Jorge Grifantini, Renata Chu, Helen Y. Veesler, David |
author_facet | Bowen, John E. Sprouse, Kaitlin R. Walls, Alexandra C. Mazzitelli, Ignacio G. Logue, Jennifer K. Franko, Nicholas M. Ahmed, Kumail Shariq, Asefa Cameroni, Elisabetta Gori, Andrea Bandera, Alessandra Posavad, Christine M. Dan, Jennifer M. Zhang, Zeli Weiskopf, Daniela Sette, Alessandro Crotty, Shane Iqbal, Najeeha Talat Corti, Davide Geffner, Jorge Grifantini, Renata Chu, Helen Y. Veesler, David |
author_sort | Bowen, John E. |
collection | PubMed |
description | The SARS-CoV-2 Omicron variant of concern comprises three sublineages designated BA.1, BA.2, and BA.3, with BA.2 steadily replacing the globally dominant BA.1. We show that the large number of BA.1 and BA.2 spike mutations severely dampen plasma neutralizing activity elicited by infection or seven clinical vaccines, with cross-neutralization of BA.2 being consistently more potent than that of BA.1, independent of the vaccine platform and number of doses. Although mRNA vaccines induced the greatest magnitude of Omicron BA.1 and BA.2 plasma neutralizing activity, administration of a booster based on the Wuhan-Hu-1 spike sequence markedly increased neutralizing antibody titers and breadth against BA.1 and BA.2 across all vaccines evaluated. Our data suggest that although BA.1 and BA.2 evade polyclonal neutralizing antibody responses, current vaccine boosting regimens may provide sufficient protection against Omicron-induced disease. |
format | Online Article Text |
id | pubmed-8936098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-89360982022-03-22 Omicron BA.1 and BA.2 neutralizing activity elicited by a comprehensive panel of human vaccines Bowen, John E. Sprouse, Kaitlin R. Walls, Alexandra C. Mazzitelli, Ignacio G. Logue, Jennifer K. Franko, Nicholas M. Ahmed, Kumail Shariq, Asefa Cameroni, Elisabetta Gori, Andrea Bandera, Alessandra Posavad, Christine M. Dan, Jennifer M. Zhang, Zeli Weiskopf, Daniela Sette, Alessandro Crotty, Shane Iqbal, Najeeha Talat Corti, Davide Geffner, Jorge Grifantini, Renata Chu, Helen Y. Veesler, David bioRxiv Article The SARS-CoV-2 Omicron variant of concern comprises three sublineages designated BA.1, BA.2, and BA.3, with BA.2 steadily replacing the globally dominant BA.1. We show that the large number of BA.1 and BA.2 spike mutations severely dampen plasma neutralizing activity elicited by infection or seven clinical vaccines, with cross-neutralization of BA.2 being consistently more potent than that of BA.1, independent of the vaccine platform and number of doses. Although mRNA vaccines induced the greatest magnitude of Omicron BA.1 and BA.2 plasma neutralizing activity, administration of a booster based on the Wuhan-Hu-1 spike sequence markedly increased neutralizing antibody titers and breadth against BA.1 and BA.2 across all vaccines evaluated. Our data suggest that although BA.1 and BA.2 evade polyclonal neutralizing antibody responses, current vaccine boosting regimens may provide sufficient protection against Omicron-induced disease. Cold Spring Harbor Laboratory 2022-03-16 /pmc/articles/PMC8936098/ /pubmed/35313570 http://dx.doi.org/10.1101/2022.03.15.484542 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Bowen, John E. Sprouse, Kaitlin R. Walls, Alexandra C. Mazzitelli, Ignacio G. Logue, Jennifer K. Franko, Nicholas M. Ahmed, Kumail Shariq, Asefa Cameroni, Elisabetta Gori, Andrea Bandera, Alessandra Posavad, Christine M. Dan, Jennifer M. Zhang, Zeli Weiskopf, Daniela Sette, Alessandro Crotty, Shane Iqbal, Najeeha Talat Corti, Davide Geffner, Jorge Grifantini, Renata Chu, Helen Y. Veesler, David Omicron BA.1 and BA.2 neutralizing activity elicited by a comprehensive panel of human vaccines |
title | Omicron BA.1 and BA.2 neutralizing activity elicited by a comprehensive panel of human vaccines |
title_full | Omicron BA.1 and BA.2 neutralizing activity elicited by a comprehensive panel of human vaccines |
title_fullStr | Omicron BA.1 and BA.2 neutralizing activity elicited by a comprehensive panel of human vaccines |
title_full_unstemmed | Omicron BA.1 and BA.2 neutralizing activity elicited by a comprehensive panel of human vaccines |
title_short | Omicron BA.1 and BA.2 neutralizing activity elicited by a comprehensive panel of human vaccines |
title_sort | omicron ba.1 and ba.2 neutralizing activity elicited by a comprehensive panel of human vaccines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8936098/ https://www.ncbi.nlm.nih.gov/pubmed/35313570 http://dx.doi.org/10.1101/2022.03.15.484542 |
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