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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...

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Autores principales: Amanat, Fatima, Strohmeier, Shirin, Meade, Philip S., Dambrauskas, Nicholas, Mühlemann, Barbara, Smith, Derek J., Vigdorovich, Vladimir, Sather, D. Noah, Coughlan, Lynda, Krammer, Florian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
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.
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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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