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Sequentially immune‐induced antibodies could cross‐neutralize SARS‐CoV‐2 variants

BACKGROUND: The Omicron (B.1.1.529) SARS‐COV‐2 variant has raised serious concerns because of its unprecedented rapid rate of spreading and the fact that there are 36 mutations in the spike protein. Since the vaccine‐induced neutralizing antibody targets are the spike protein, this may lead to the p...

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Autores principales: Lv, Qi, Zhou, Shasha, Qi, Feifei, Zhang, Yaqing, Li, Fengdi, Liu, Mingya, Bao, Linlin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879626/
https://www.ncbi.nlm.nih.gov/pubmed/35213787
http://dx.doi.org/10.1002/ame2.12216
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author Lv, Qi
Zhou, Shasha
Qi, Feifei
Zhang, Yaqing
Li, Fengdi
Liu, Mingya
Bao, Linlin
author_facet Lv, Qi
Zhou, Shasha
Qi, Feifei
Zhang, Yaqing
Li, Fengdi
Liu, Mingya
Bao, Linlin
author_sort Lv, Qi
collection PubMed
description BACKGROUND: The Omicron (B.1.1.529) SARS‐COV‐2 variant has raised serious concerns because of its unprecedented rapid rate of spreading and the fact that there are 36 mutations in the spike protein. Since the vaccine‐induced neutralizing antibody targets are the spike protein, this may lead to the possibility of vaccine‐induced humoral immunity escape. METHODS: We measured the neutralizing activity in vitro for Omicron and compared this with wild type (WH‐09) and Delta variants in human and monkey sera from different types of immunity. The monkey sera samples were collected at 1 and 3 months post three‐dose inactivated (PiCoVacc) and recombinant protein (ZF2001) vaccination. Human sera were collected from 1 month post three‐dose inactivated vaccination. RESULTS: In inactivated vaccine sera, at 1/3 months post three‐dose, geometric mean titers (GMTs) of neutralization antibody (NAb) against the Omicron variant were 4.9/5.2‐fold lower than those of the wild type. In recombinant protein vaccine sera, GMTs of NAb against Omicron were 15.7/8.9‐fold lower than those of the wild type. In human sera, at 1 month post three‐dose inactivated vaccination, GMTs of NAb against Omicron were 3.1‐fold lower than those of the wild type. CONCLUSION: This study demonstrated that despite a reduction in neutralization titers, cross‐neutralizing activity against Omicron and Delta variants was still observed after three doses of inactivated and recombinant protein vaccination.
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spelling pubmed-88796262022-03-01 Sequentially immune‐induced antibodies could cross‐neutralize SARS‐CoV‐2 variants Lv, Qi Zhou, Shasha Qi, Feifei Zhang, Yaqing Li, Fengdi Liu, Mingya Bao, Linlin Animal Model Exp Med Regular Articles BACKGROUND: The Omicron (B.1.1.529) SARS‐COV‐2 variant has raised serious concerns because of its unprecedented rapid rate of spreading and the fact that there are 36 mutations in the spike protein. Since the vaccine‐induced neutralizing antibody targets are the spike protein, this may lead to the possibility of vaccine‐induced humoral immunity escape. METHODS: We measured the neutralizing activity in vitro for Omicron and compared this with wild type (WH‐09) and Delta variants in human and monkey sera from different types of immunity. The monkey sera samples were collected at 1 and 3 months post three‐dose inactivated (PiCoVacc) and recombinant protein (ZF2001) vaccination. Human sera were collected from 1 month post three‐dose inactivated vaccination. RESULTS: In inactivated vaccine sera, at 1/3 months post three‐dose, geometric mean titers (GMTs) of neutralization antibody (NAb) against the Omicron variant were 4.9/5.2‐fold lower than those of the wild type. In recombinant protein vaccine sera, GMTs of NAb against Omicron were 15.7/8.9‐fold lower than those of the wild type. In human sera, at 1 month post three‐dose inactivated vaccination, GMTs of NAb against Omicron were 3.1‐fold lower than those of the wild type. CONCLUSION: This study demonstrated that despite a reduction in neutralization titers, cross‐neutralizing activity against Omicron and Delta variants was still observed after three doses of inactivated and recombinant protein vaccination. John Wiley and Sons Inc. 2022-02-25 /pmc/articles/PMC8879626/ /pubmed/35213787 http://dx.doi.org/10.1002/ame2.12216 Text en © 2022 The Authors. Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Regular Articles
Lv, Qi
Zhou, Shasha
Qi, Feifei
Zhang, Yaqing
Li, Fengdi
Liu, Mingya
Bao, Linlin
Sequentially immune‐induced antibodies could cross‐neutralize SARS‐CoV‐2 variants
title Sequentially immune‐induced antibodies could cross‐neutralize SARS‐CoV‐2 variants
title_full Sequentially immune‐induced antibodies could cross‐neutralize SARS‐CoV‐2 variants
title_fullStr Sequentially immune‐induced antibodies could cross‐neutralize SARS‐CoV‐2 variants
title_full_unstemmed Sequentially immune‐induced antibodies could cross‐neutralize SARS‐CoV‐2 variants
title_short Sequentially immune‐induced antibodies could cross‐neutralize SARS‐CoV‐2 variants
title_sort sequentially immune‐induced antibodies could cross‐neutralize sars‐cov‐2 variants
topic Regular Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879626/
https://www.ncbi.nlm.nih.gov/pubmed/35213787
http://dx.doi.org/10.1002/ame2.12216
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