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Multiple SARS-CoV-2 variants escape neutralization by vaccine-induced humoral immunity
Vaccination elicits immune responses capable of potently neutralizing SARS-CoV-2. However, ongoing surveillance has revealed the emergence of variants harboring mutations in spike, the main target of neutralizing antibodies. To understand the impact of these variants, we evaluated the neutralization...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953441/ https://www.ncbi.nlm.nih.gov/pubmed/33743213 http://dx.doi.org/10.1016/j.cell.2021.03.013 |
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author | Garcia-Beltran, Wilfredo F. Lam, Evan C. St. Denis, Kerri Nitido, Adam D. Garcia, Zeidy H. Hauser, Blake M. Feldman, Jared Pavlovic, Maia N. Gregory, David J. Poznansky, Mark C. Sigal, Alex Schmidt, Aaron G. Iafrate, A. John Naranbhai, Vivek Balazs, Alejandro B. |
author_facet | Garcia-Beltran, Wilfredo F. Lam, Evan C. St. Denis, Kerri Nitido, Adam D. Garcia, Zeidy H. Hauser, Blake M. Feldman, Jared Pavlovic, Maia N. Gregory, David J. Poznansky, Mark C. Sigal, Alex Schmidt, Aaron G. Iafrate, A. John Naranbhai, Vivek Balazs, Alejandro B. |
author_sort | Garcia-Beltran, Wilfredo F. |
collection | PubMed |
description | Vaccination elicits immune responses capable of potently neutralizing SARS-CoV-2. However, ongoing surveillance has revealed the emergence of variants harboring mutations in spike, the main target of neutralizing antibodies. To understand the impact of these variants, we evaluated the neutralization potency of 99 individuals that received one or two doses of either BNT162b2 or mRNA-1273 vaccines against pseudoviruses representing 10 globally circulating strains of SARS-CoV-2. Five of the 10 pseudoviruses, harboring receptor-binding domain mutations, including K417N/T, E484K, and N501Y, were highly resistant to neutralization. Cross-neutralization of B.1.351 variants was comparable to SARS-CoV and bat-derived WIV1-CoV, suggesting that a relatively small number of mutations can mediate potent escape from vaccine responses. While the clinical impact of neutralization resistance remains uncertain, these results highlight the potential for variants to escape from neutralizing humoral immunity and emphasize the need to develop broadly protective interventions against the evolving pandemic. |
format | Online Article Text |
id | pubmed-7953441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-79534412021-03-12 Multiple SARS-CoV-2 variants escape neutralization by vaccine-induced humoral immunity Garcia-Beltran, Wilfredo F. Lam, Evan C. St. Denis, Kerri Nitido, Adam D. Garcia, Zeidy H. Hauser, Blake M. Feldman, Jared Pavlovic, Maia N. Gregory, David J. Poznansky, Mark C. Sigal, Alex Schmidt, Aaron G. Iafrate, A. John Naranbhai, Vivek Balazs, Alejandro B. Cell Article Vaccination elicits immune responses capable of potently neutralizing SARS-CoV-2. However, ongoing surveillance has revealed the emergence of variants harboring mutations in spike, the main target of neutralizing antibodies. To understand the impact of these variants, we evaluated the neutralization potency of 99 individuals that received one or two doses of either BNT162b2 or mRNA-1273 vaccines against pseudoviruses representing 10 globally circulating strains of SARS-CoV-2. Five of the 10 pseudoviruses, harboring receptor-binding domain mutations, including K417N/T, E484K, and N501Y, were highly resistant to neutralization. Cross-neutralization of B.1.351 variants was comparable to SARS-CoV and bat-derived WIV1-CoV, suggesting that a relatively small number of mutations can mediate potent escape from vaccine responses. While the clinical impact of neutralization resistance remains uncertain, these results highlight the potential for variants to escape from neutralizing humoral immunity and emphasize the need to develop broadly protective interventions against the evolving pandemic. Cell Press 2021-04-29 /pmc/articles/PMC7953441/ /pubmed/33743213 http://dx.doi.org/10.1016/j.cell.2021.03.013 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Garcia-Beltran, Wilfredo F. Lam, Evan C. St. Denis, Kerri Nitido, Adam D. Garcia, Zeidy H. Hauser, Blake M. Feldman, Jared Pavlovic, Maia N. Gregory, David J. Poznansky, Mark C. Sigal, Alex Schmidt, Aaron G. Iafrate, A. John Naranbhai, Vivek Balazs, Alejandro B. Multiple SARS-CoV-2 variants escape neutralization by vaccine-induced humoral immunity |
title | Multiple SARS-CoV-2 variants escape neutralization by vaccine-induced humoral immunity |
title_full | Multiple SARS-CoV-2 variants escape neutralization by vaccine-induced humoral immunity |
title_fullStr | Multiple SARS-CoV-2 variants escape neutralization by vaccine-induced humoral immunity |
title_full_unstemmed | Multiple SARS-CoV-2 variants escape neutralization by vaccine-induced humoral immunity |
title_short | Multiple SARS-CoV-2 variants escape neutralization by vaccine-induced humoral immunity |
title_sort | multiple sars-cov-2 variants escape neutralization by vaccine-induced humoral immunity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953441/ https://www.ncbi.nlm.nih.gov/pubmed/33743213 http://dx.doi.org/10.1016/j.cell.2021.03.013 |
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