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SARS-CoV-2 bivalent mRNA vaccine with broad protection against variants of concern

INTRODUCTION: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant has rapidly spread around the globe. With a substantial number of mutations in its Spike protein, the SARS-CoV-2 Omicron variant is prone to immune evasion and led to the reduced efficacy of approved vacci...

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Autores principales: Ma, Qinhai, Li, Man, Ma, Lin, Zhang, Caroline, Zhang, Hong, Zhong, Huiling, Wen, Jian, Wang, Yongsheng, Yan, Zewei, Xiong, Wei, Wu, Linping, Guo, Jianmin, Yang, Wei, Yang, Zifeng, Zhang, Biliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244545/
https://www.ncbi.nlm.nih.gov/pubmed/37292197
http://dx.doi.org/10.3389/fimmu.2023.1195299
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author Ma, Qinhai
Li, Man
Ma, Lin
Zhang, Caroline
Zhang, Hong
Zhong, Huiling
Wen, Jian
Wang, Yongsheng
Yan, Zewei
Xiong, Wei
Wu, Linping
Guo, Jianmin
Yang, Wei
Yang, Zifeng
Zhang, Biliang
author_facet Ma, Qinhai
Li, Man
Ma, Lin
Zhang, Caroline
Zhang, Hong
Zhong, Huiling
Wen, Jian
Wang, Yongsheng
Yan, Zewei
Xiong, Wei
Wu, Linping
Guo, Jianmin
Yang, Wei
Yang, Zifeng
Zhang, Biliang
author_sort Ma, Qinhai
collection PubMed
description INTRODUCTION: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant has rapidly spread around the globe. With a substantial number of mutations in its Spike protein, the SARS-CoV-2 Omicron variant is prone to immune evasion and led to the reduced efficacy of approved vaccines. Thus, emerging variants have brought new challenges to the prevention of COVID-19 and updated vaccines are urgently needed to provide better protection against the Omicron variant or other highly mutated variants. MATERIALS AND METHODS: Here, we developed a novel bivalent mRNA vaccine, RBMRNA-405, comprising a 1:1 mix of mRNAs encoding both Delta-derived and Omicron-derived Spike proteins. We evaluated the immunogenicity of RBMRNA-405 in BALB/c mice and compared the antibody response and prophylactic efficacy induced by monovalent Delta or Omicron-specific vaccine with the bivalent RBMRNA-405 vaccine in the SARSCoV-2 variant challenge. RESULTS: Results showed that the RBMRNA-405 vaccine could generate broader neutralizing antibody responses against both Wuhan-Hu-1 and other SARS-CoV-2 variants, including Delta, Omicron, Alpha, Beta, and Gamma. RBMRNA-405 efficiently blocked infectious viral replication and lung injury in both Omicron- and Delta-challenged K18-ACE2 mice. CONCLUSION: Our data suggest that RBMRNA-405 is a promising bivalent SARS-CoV-2 vaccine with broad-spectrum efficacy for further clinical development.
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spelling pubmed-102445452023-06-08 SARS-CoV-2 bivalent mRNA vaccine with broad protection against variants of concern Ma, Qinhai Li, Man Ma, Lin Zhang, Caroline Zhang, Hong Zhong, Huiling Wen, Jian Wang, Yongsheng Yan, Zewei Xiong, Wei Wu, Linping Guo, Jianmin Yang, Wei Yang, Zifeng Zhang, Biliang Front Immunol Immunology INTRODUCTION: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant has rapidly spread around the globe. With a substantial number of mutations in its Spike protein, the SARS-CoV-2 Omicron variant is prone to immune evasion and led to the reduced efficacy of approved vaccines. Thus, emerging variants have brought new challenges to the prevention of COVID-19 and updated vaccines are urgently needed to provide better protection against the Omicron variant or other highly mutated variants. MATERIALS AND METHODS: Here, we developed a novel bivalent mRNA vaccine, RBMRNA-405, comprising a 1:1 mix of mRNAs encoding both Delta-derived and Omicron-derived Spike proteins. We evaluated the immunogenicity of RBMRNA-405 in BALB/c mice and compared the antibody response and prophylactic efficacy induced by monovalent Delta or Omicron-specific vaccine with the bivalent RBMRNA-405 vaccine in the SARSCoV-2 variant challenge. RESULTS: Results showed that the RBMRNA-405 vaccine could generate broader neutralizing antibody responses against both Wuhan-Hu-1 and other SARS-CoV-2 variants, including Delta, Omicron, Alpha, Beta, and Gamma. RBMRNA-405 efficiently blocked infectious viral replication and lung injury in both Omicron- and Delta-challenged K18-ACE2 mice. CONCLUSION: Our data suggest that RBMRNA-405 is a promising bivalent SARS-CoV-2 vaccine with broad-spectrum efficacy for further clinical development. Frontiers Media S.A. 2023-05-24 /pmc/articles/PMC10244545/ /pubmed/37292197 http://dx.doi.org/10.3389/fimmu.2023.1195299 Text en Copyright © 2023 Ma, Li, Ma, Zhang, Zhang, Zhong, Wen, Wang, Yan, Xiong, Wu, Guo, Yang, Yang and Zhang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Ma, Qinhai
Li, Man
Ma, Lin
Zhang, Caroline
Zhang, Hong
Zhong, Huiling
Wen, Jian
Wang, Yongsheng
Yan, Zewei
Xiong, Wei
Wu, Linping
Guo, Jianmin
Yang, Wei
Yang, Zifeng
Zhang, Biliang
SARS-CoV-2 bivalent mRNA vaccine with broad protection against variants of concern
title SARS-CoV-2 bivalent mRNA vaccine with broad protection against variants of concern
title_full SARS-CoV-2 bivalent mRNA vaccine with broad protection against variants of concern
title_fullStr SARS-CoV-2 bivalent mRNA vaccine with broad protection against variants of concern
title_full_unstemmed SARS-CoV-2 bivalent mRNA vaccine with broad protection against variants of concern
title_short SARS-CoV-2 bivalent mRNA vaccine with broad protection against variants of concern
title_sort sars-cov-2 bivalent mrna vaccine with broad protection against variants of concern
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244545/
https://www.ncbi.nlm.nih.gov/pubmed/37292197
http://dx.doi.org/10.3389/fimmu.2023.1195299
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