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Heterologous immunization with inactivated vaccine followed by mRNA-booster elicits strong immunity against SARS-CoV-2 Omicron variant

The recent emergence of the Omicron variant has raised concerns on vaccine efficacy and the urgent need to study more efficient vaccination strategies. Here we observed that an mRNA vaccine booster in individuals vaccinated with two doses of inactivated vaccine significantly increased the plasma lev...

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Autores principales: Zuo, Fanglei, Abolhassani, Hassan, Du, Likun, Piralla, Antonio, Bertoglio, Federico, de Campos-Mata, Leire, Wan, Hui, Schubert, Maren, Cassaniti, Irene, Wang, Yating, Sammartino, Josè Camilla, Sun, Rui, Vlachiotis, Stelios, Bergami, Federica, Kumagai-Braesch, Makiko, Andréll, Juni, Zhang, Zhaoxia, Xue, Yintong, Wenzel, Esther Veronika, Calzolai, Luigi, Varani, Luca, Rezaei, Nima, Chavoshzadeh, Zahra, Baldanti, Fausto, Hust, Michael, Hammarström, Lennart, Marcotte, Harold, Pan-Hammarström, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9106736/
https://www.ncbi.nlm.nih.gov/pubmed/35562366
http://dx.doi.org/10.1038/s41467-022-30340-5
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author Zuo, Fanglei
Abolhassani, Hassan
Du, Likun
Piralla, Antonio
Bertoglio, Federico
de Campos-Mata, Leire
Wan, Hui
Schubert, Maren
Cassaniti, Irene
Wang, Yating
Sammartino, Josè Camilla
Sun, Rui
Vlachiotis, Stelios
Bergami, Federica
Kumagai-Braesch, Makiko
Andréll, Juni
Zhang, Zhaoxia
Xue, Yintong
Wenzel, Esther Veronika
Calzolai, Luigi
Varani, Luca
Rezaei, Nima
Chavoshzadeh, Zahra
Baldanti, Fausto
Hust, Michael
Hammarström, Lennart
Marcotte, Harold
Pan-Hammarström, Qiang
author_facet Zuo, Fanglei
Abolhassani, Hassan
Du, Likun
Piralla, Antonio
Bertoglio, Federico
de Campos-Mata, Leire
Wan, Hui
Schubert, Maren
Cassaniti, Irene
Wang, Yating
Sammartino, Josè Camilla
Sun, Rui
Vlachiotis, Stelios
Bergami, Federica
Kumagai-Braesch, Makiko
Andréll, Juni
Zhang, Zhaoxia
Xue, Yintong
Wenzel, Esther Veronika
Calzolai, Luigi
Varani, Luca
Rezaei, Nima
Chavoshzadeh, Zahra
Baldanti, Fausto
Hust, Michael
Hammarström, Lennart
Marcotte, Harold
Pan-Hammarström, Qiang
author_sort Zuo, Fanglei
collection PubMed
description The recent emergence of the Omicron variant has raised concerns on vaccine efficacy and the urgent need to study more efficient vaccination strategies. Here we observed that an mRNA vaccine booster in individuals vaccinated with two doses of inactivated vaccine significantly increased the plasma level of specific antibodies that bind to the receptor-binding domain (RBD) or the spike (S) ectodomain (S1 + S2) of both the G614 and the Omicron variants, compared to two doses of homologous inactivated vaccine. The level of RBD- and S-specific IgG antibodies and virus neutralization titers against variants of concern in the heterologous vaccination group were similar to that in individuals receiving three doses of homologous mRNA-vaccine or a boost of mRNA vaccine after infection, but markedly higher than that in individuals receiving three doses of a homologous inactivated vaccine. This heterologous vaccination regime furthermore significantly enhanced the RBD-specific memory B cell response and S1-specific T cell response, compared to two or three doses of homologous inactivated vaccine. Our study demonstrates that mRNA vaccine booster in individuals vaccinated with inactivated vaccines can be highly beneficial, as it markedly increases the humoral and cellular immune responses against the virus, including the Omicron variant.
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spelling pubmed-91067362022-05-15 Heterologous immunization with inactivated vaccine followed by mRNA-booster elicits strong immunity against SARS-CoV-2 Omicron variant Zuo, Fanglei Abolhassani, Hassan Du, Likun Piralla, Antonio Bertoglio, Federico de Campos-Mata, Leire Wan, Hui Schubert, Maren Cassaniti, Irene Wang, Yating Sammartino, Josè Camilla Sun, Rui Vlachiotis, Stelios Bergami, Federica Kumagai-Braesch, Makiko Andréll, Juni Zhang, Zhaoxia Xue, Yintong Wenzel, Esther Veronika Calzolai, Luigi Varani, Luca Rezaei, Nima Chavoshzadeh, Zahra Baldanti, Fausto Hust, Michael Hammarström, Lennart Marcotte, Harold Pan-Hammarström, Qiang Nat Commun Article The recent emergence of the Omicron variant has raised concerns on vaccine efficacy and the urgent need to study more efficient vaccination strategies. Here we observed that an mRNA vaccine booster in individuals vaccinated with two doses of inactivated vaccine significantly increased the plasma level of specific antibodies that bind to the receptor-binding domain (RBD) or the spike (S) ectodomain (S1 + S2) of both the G614 and the Omicron variants, compared to two doses of homologous inactivated vaccine. The level of RBD- and S-specific IgG antibodies and virus neutralization titers against variants of concern in the heterologous vaccination group were similar to that in individuals receiving three doses of homologous mRNA-vaccine or a boost of mRNA vaccine after infection, but markedly higher than that in individuals receiving three doses of a homologous inactivated vaccine. This heterologous vaccination regime furthermore significantly enhanced the RBD-specific memory B cell response and S1-specific T cell response, compared to two or three doses of homologous inactivated vaccine. Our study demonstrates that mRNA vaccine booster in individuals vaccinated with inactivated vaccines can be highly beneficial, as it markedly increases the humoral and cellular immune responses against the virus, including the Omicron variant. Nature Publishing Group UK 2022-05-13 /pmc/articles/PMC9106736/ /pubmed/35562366 http://dx.doi.org/10.1038/s41467-022-30340-5 Text en © The Author(s) 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 Article
Zuo, Fanglei
Abolhassani, Hassan
Du, Likun
Piralla, Antonio
Bertoglio, Federico
de Campos-Mata, Leire
Wan, Hui
Schubert, Maren
Cassaniti, Irene
Wang, Yating
Sammartino, Josè Camilla
Sun, Rui
Vlachiotis, Stelios
Bergami, Federica
Kumagai-Braesch, Makiko
Andréll, Juni
Zhang, Zhaoxia
Xue, Yintong
Wenzel, Esther Veronika
Calzolai, Luigi
Varani, Luca
Rezaei, Nima
Chavoshzadeh, Zahra
Baldanti, Fausto
Hust, Michael
Hammarström, Lennart
Marcotte, Harold
Pan-Hammarström, Qiang
Heterologous immunization with inactivated vaccine followed by mRNA-booster elicits strong immunity against SARS-CoV-2 Omicron variant
title Heterologous immunization with inactivated vaccine followed by mRNA-booster elicits strong immunity against SARS-CoV-2 Omicron variant
title_full Heterologous immunization with inactivated vaccine followed by mRNA-booster elicits strong immunity against SARS-CoV-2 Omicron variant
title_fullStr Heterologous immunization with inactivated vaccine followed by mRNA-booster elicits strong immunity against SARS-CoV-2 Omicron variant
title_full_unstemmed Heterologous immunization with inactivated vaccine followed by mRNA-booster elicits strong immunity against SARS-CoV-2 Omicron variant
title_short Heterologous immunization with inactivated vaccine followed by mRNA-booster elicits strong immunity against SARS-CoV-2 Omicron variant
title_sort heterologous immunization with inactivated vaccine followed by mrna-booster elicits strong immunity against sars-cov-2 omicron variant
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9106736/
https://www.ncbi.nlm.nih.gov/pubmed/35562366
http://dx.doi.org/10.1038/s41467-022-30340-5
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