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Vaccination with SARS-CoV-2 variants of concern protects mice from challenge with wild-type virus
Vaccines against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) have been highly efficient in protecting against Coronavirus Disease 2019 (COVID-19). However, the emergence of viral variants that are more transmissible and, in some cases, escape from neutralizing antibody responses has...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8758087/ https://www.ncbi.nlm.nih.gov/pubmed/34914685 http://dx.doi.org/10.1371/journal.pbio.3001384 |
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author | Amanat, Fatima Strohmeier, Shirin Meade, Philip S. Dambrauskas, Nicholas Mühlemann, Barbara Smith, Derek J. Vigdorovich, Vladimir Sather, D. Noah Coughlan, Lynda Krammer, Florian |
author_facet | Amanat, Fatima Strohmeier, Shirin Meade, Philip S. Dambrauskas, Nicholas Mühlemann, Barbara Smith, Derek J. Vigdorovich, Vladimir Sather, D. Noah Coughlan, Lynda Krammer, Florian |
author_sort | Amanat, Fatima |
collection | PubMed |
description | Vaccines against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) have been highly efficient in protecting against Coronavirus Disease 2019 (COVID-19). However, the emergence of viral variants that are more transmissible and, in some cases, escape from neutralizing antibody responses has raised concerns. Here, we evaluated recombinant protein spike antigens derived from wild-type SARS-CoV-2 and from variants B.1.1.7, B.1.351, and P.1 for their immunogenicity and protective effect in vivo against challenge with wild-type SARS-CoV-2 in the mouse model. All proteins induced high neutralizing antibodies against the respective viruses but also induced high cross-neutralizing antibody responses. The decline in neutralizing titers between variants was moderate, with B.1.1.7-vaccinated animals having a maximum fold reduction of 4.8 against B.1.351 virus. P.1 induced the most cross-reactive antibody responses but was also the least immunogenic in terms of homologous neutralization titers. However, all antigens protected from challenge with wild-type SARS-CoV-2 in a mouse model. |
format | Online Article Text |
id | pubmed-8758087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-87580872022-01-14 Vaccination with SARS-CoV-2 variants of concern protects mice from challenge with wild-type virus Amanat, Fatima Strohmeier, Shirin Meade, Philip S. Dambrauskas, Nicholas Mühlemann, Barbara Smith, Derek J. Vigdorovich, Vladimir Sather, D. Noah Coughlan, Lynda Krammer, Florian PLoS Biol Research Article Vaccines against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) have been highly efficient in protecting against Coronavirus Disease 2019 (COVID-19). However, the emergence of viral variants that are more transmissible and, in some cases, escape from neutralizing antibody responses has raised concerns. Here, we evaluated recombinant protein spike antigens derived from wild-type SARS-CoV-2 and from variants B.1.1.7, B.1.351, and P.1 for their immunogenicity and protective effect in vivo against challenge with wild-type SARS-CoV-2 in the mouse model. All proteins induced high neutralizing antibodies against the respective viruses but also induced high cross-neutralizing antibody responses. The decline in neutralizing titers between variants was moderate, with B.1.1.7-vaccinated animals having a maximum fold reduction of 4.8 against B.1.351 virus. P.1 induced the most cross-reactive antibody responses but was also the least immunogenic in terms of homologous neutralization titers. However, all antigens protected from challenge with wild-type SARS-CoV-2 in a mouse model. Public Library of Science 2021-12-16 /pmc/articles/PMC8758087/ /pubmed/34914685 http://dx.doi.org/10.1371/journal.pbio.3001384 Text en © 2021 Amanat et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Amanat, Fatima Strohmeier, Shirin Meade, Philip S. Dambrauskas, Nicholas Mühlemann, Barbara Smith, Derek J. Vigdorovich, Vladimir Sather, D. Noah Coughlan, Lynda Krammer, Florian Vaccination with SARS-CoV-2 variants of concern protects mice from challenge with wild-type virus |
title | Vaccination with SARS-CoV-2 variants of concern protects mice from challenge with wild-type virus |
title_full | Vaccination with SARS-CoV-2 variants of concern protects mice from challenge with wild-type virus |
title_fullStr | Vaccination with SARS-CoV-2 variants of concern protects mice from challenge with wild-type virus |
title_full_unstemmed | Vaccination with SARS-CoV-2 variants of concern protects mice from challenge with wild-type virus |
title_short | Vaccination with SARS-CoV-2 variants of concern protects mice from challenge with wild-type virus |
title_sort | vaccination with sars-cov-2 variants of concern protects mice from challenge with wild-type virus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8758087/ https://www.ncbi.nlm.nih.gov/pubmed/34914685 http://dx.doi.org/10.1371/journal.pbio.3001384 |
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