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Heterologous boost with mRNA vaccines against SARS-CoV-2 Delta/Omicron variants following an inactivated whole-virus vaccine

The coronavirus SARS-CoV-2 has mutated quickly and caused significant global damage. This study characterizes two mRNA vaccines ZSVG-02 (Delta) and ZSVG-02-O (Omicron BA.1), and associating heterologous prime-boost strategy following the prime of a most widely administrated inactivated whole-virus v...

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Autores principales: Lu, Changrui, Zhang, Yuntao, Liu, Xiaohu, Hou, Fujun, Cai, Rujie, Yu, Zhibin, Liu, Fei, Yang, Guohuan, Ding, Jun, Xu, Jiang, Hua, Xianwu, Cheng, Xinhua, Pan, Xinping, Liu, Lianxiao, Lin, Kang, Wang, Zejun, Li, Xinguo, Lu, Jia, Zhang, Qiu, Li, Yuwei, Hu, Chunxia, Fan, Huifen, Liu, Xiaoke, Wang, Hui, Jia, Rui, Xu, Fangjingwei, Wang, Xuewei, Huang, Hongwei, Zhao, Ronghua, Li, Jing, Cheng, Hang, Jia, William, Yang, Xiaoming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier B.V. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985518/
https://www.ncbi.nlm.nih.gov/pubmed/36871919
http://dx.doi.org/10.1016/j.antiviral.2023.105556
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author Lu, Changrui
Zhang, Yuntao
Liu, Xiaohu
Hou, Fujun
Cai, Rujie
Yu, Zhibin
Liu, Fei
Yang, Guohuan
Ding, Jun
Xu, Jiang
Hua, Xianwu
Cheng, Xinhua
Pan, Xinping
Liu, Lianxiao
Lin, Kang
Wang, Zejun
Li, Xinguo
Lu, Jia
Zhang, Qiu
Li, Yuwei
Hu, Chunxia
Fan, Huifen
Liu, Xiaoke
Wang, Hui
Jia, Rui
Xu, Fangjingwei
Wang, Xuewei
Huang, Hongwei
Zhao, Ronghua
Li, Jing
Cheng, Hang
Jia, William
Yang, Xiaoming
author_facet Lu, Changrui
Zhang, Yuntao
Liu, Xiaohu
Hou, Fujun
Cai, Rujie
Yu, Zhibin
Liu, Fei
Yang, Guohuan
Ding, Jun
Xu, Jiang
Hua, Xianwu
Cheng, Xinhua
Pan, Xinping
Liu, Lianxiao
Lin, Kang
Wang, Zejun
Li, Xinguo
Lu, Jia
Zhang, Qiu
Li, Yuwei
Hu, Chunxia
Fan, Huifen
Liu, Xiaoke
Wang, Hui
Jia, Rui
Xu, Fangjingwei
Wang, Xuewei
Huang, Hongwei
Zhao, Ronghua
Li, Jing
Cheng, Hang
Jia, William
Yang, Xiaoming
author_sort Lu, Changrui
collection PubMed
description The coronavirus SARS-CoV-2 has mutated quickly and caused significant global damage. This study characterizes two mRNA vaccines ZSVG-02 (Delta) and ZSVG-02-O (Omicron BA.1), and associating heterologous prime-boost strategy following the prime of a most widely administrated inactivated whole-virus vaccine (BBIBP-CorV). The ZSVG-02-O induces neutralizing antibodies that effectively cross-react with Omicron subvariants. In naïve animals, ZSVG-02 or ZSVG-02-O induce humoral responses skewed to the vaccine's targeting strains, but cellular immune responses cross-react to all variants of concern (VOCs) tested. Following heterologous prime-boost regimes, animals present comparable neutralizing antibody levels and superior protection against Delta and Omicron BA.1variants. Single-boost only generated ancestral and omicron dual-responsive antibodies, probably by “recall” and “reshape” the prime immunity. New Omicron-specific antibody populations, however, appeared only following the second boost with ZSVG-02-O. Overall, our results support a heterologous boost with ZSVG-02-O, providing the best protection against current VOCs in inactivated virus vaccine–primed populations.
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spelling pubmed-99855182023-03-06 Heterologous boost with mRNA vaccines against SARS-CoV-2 Delta/Omicron variants following an inactivated whole-virus vaccine Lu, Changrui Zhang, Yuntao Liu, Xiaohu Hou, Fujun Cai, Rujie Yu, Zhibin Liu, Fei Yang, Guohuan Ding, Jun Xu, Jiang Hua, Xianwu Cheng, Xinhua Pan, Xinping Liu, Lianxiao Lin, Kang Wang, Zejun Li, Xinguo Lu, Jia Zhang, Qiu Li, Yuwei Hu, Chunxia Fan, Huifen Liu, Xiaoke Wang, Hui Jia, Rui Xu, Fangjingwei Wang, Xuewei Huang, Hongwei Zhao, Ronghua Li, Jing Cheng, Hang Jia, William Yang, Xiaoming Antiviral Res Article The coronavirus SARS-CoV-2 has mutated quickly and caused significant global damage. This study characterizes two mRNA vaccines ZSVG-02 (Delta) and ZSVG-02-O (Omicron BA.1), and associating heterologous prime-boost strategy following the prime of a most widely administrated inactivated whole-virus vaccine (BBIBP-CorV). The ZSVG-02-O induces neutralizing antibodies that effectively cross-react with Omicron subvariants. In naïve animals, ZSVG-02 or ZSVG-02-O induce humoral responses skewed to the vaccine's targeting strains, but cellular immune responses cross-react to all variants of concern (VOCs) tested. Following heterologous prime-boost regimes, animals present comparable neutralizing antibody levels and superior protection against Delta and Omicron BA.1variants. Single-boost only generated ancestral and omicron dual-responsive antibodies, probably by “recall” and “reshape” the prime immunity. New Omicron-specific antibody populations, however, appeared only following the second boost with ZSVG-02-O. Overall, our results support a heterologous boost with ZSVG-02-O, providing the best protection against current VOCs in inactivated virus vaccine–primed populations. The Authors. Published by Elsevier B.V. 2023-04 2023-03-05 /pmc/articles/PMC9985518/ /pubmed/36871919 http://dx.doi.org/10.1016/j.antiviral.2023.105556 Text en © 2023 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Lu, Changrui
Zhang, Yuntao
Liu, Xiaohu
Hou, Fujun
Cai, Rujie
Yu, Zhibin
Liu, Fei
Yang, Guohuan
Ding, Jun
Xu, Jiang
Hua, Xianwu
Cheng, Xinhua
Pan, Xinping
Liu, Lianxiao
Lin, Kang
Wang, Zejun
Li, Xinguo
Lu, Jia
Zhang, Qiu
Li, Yuwei
Hu, Chunxia
Fan, Huifen
Liu, Xiaoke
Wang, Hui
Jia, Rui
Xu, Fangjingwei
Wang, Xuewei
Huang, Hongwei
Zhao, Ronghua
Li, Jing
Cheng, Hang
Jia, William
Yang, Xiaoming
Heterologous boost with mRNA vaccines against SARS-CoV-2 Delta/Omicron variants following an inactivated whole-virus vaccine
title Heterologous boost with mRNA vaccines against SARS-CoV-2 Delta/Omicron variants following an inactivated whole-virus vaccine
title_full Heterologous boost with mRNA vaccines against SARS-CoV-2 Delta/Omicron variants following an inactivated whole-virus vaccine
title_fullStr Heterologous boost with mRNA vaccines against SARS-CoV-2 Delta/Omicron variants following an inactivated whole-virus vaccine
title_full_unstemmed Heterologous boost with mRNA vaccines against SARS-CoV-2 Delta/Omicron variants following an inactivated whole-virus vaccine
title_short Heterologous boost with mRNA vaccines against SARS-CoV-2 Delta/Omicron variants following an inactivated whole-virus vaccine
title_sort heterologous boost with mrna vaccines against sars-cov-2 delta/omicron variants following an inactivated whole-virus vaccine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985518/
https://www.ncbi.nlm.nih.gov/pubmed/36871919
http://dx.doi.org/10.1016/j.antiviral.2023.105556
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