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Immunogenicity of a vaccinia virus-based severe acute respiratory syndrome coronavirus 2 vaccine candidate
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines provide essential tools for the control of the COVID-19 pandemic. A number of technologies have been employed to develop SARS-CoV-2 vaccines, including the inactivated SARS-CoV-2 particles, mRNA to express viral spike protein, rec...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353262/ https://www.ncbi.nlm.nih.gov/pubmed/35935962 http://dx.doi.org/10.3389/fimmu.2022.911164 |
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author | Mei, Shan Fan, Zhangling Liu, Xiaoman Zhao, Fei Huang, Yu Wei, Liang Hu, Yamei Xie, Yu Wang, Liming Ai, Bin Liang, Chen Xu, Fengwen Guo, Fei |
author_facet | Mei, Shan Fan, Zhangling Liu, Xiaoman Zhao, Fei Huang, Yu Wei, Liang Hu, Yamei Xie, Yu Wang, Liming Ai, Bin Liang, Chen Xu, Fengwen Guo, Fei |
author_sort | Mei, Shan |
collection | PubMed |
description | Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines provide essential tools for the control of the COVID-19 pandemic. A number of technologies have been employed to develop SARS-CoV-2 vaccines, including the inactivated SARS-CoV-2 particles, mRNA to express viral spike protein, recombinant spike proteins, and viral vectors. Here, we report the use of the vaccinia virus Tiantan strain as a vector to express the SARS-CoV-2 spike protein. When it was used to inoculate mice, robust SARS-CoV-2 spike protein-specific antibody response and T-cell response were detected. Sera from the vaccinated mice showed strong neutralizing activity against the ancestral Wuhan SARS-CoV-2, the variants of concern (VOCs) B.1.351, B.1.617.2, and the emerging B.1.1.529 (omicron). This finding supports the possibility of developing a new type of SARS-CoV-2 vaccine using the vaccinia virus vector. |
format | Online Article Text |
id | pubmed-9353262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93532622022-08-06 Immunogenicity of a vaccinia virus-based severe acute respiratory syndrome coronavirus 2 vaccine candidate Mei, Shan Fan, Zhangling Liu, Xiaoman Zhao, Fei Huang, Yu Wei, Liang Hu, Yamei Xie, Yu Wang, Liming Ai, Bin Liang, Chen Xu, Fengwen Guo, Fei Front Immunol Immunology Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines provide essential tools for the control of the COVID-19 pandemic. A number of technologies have been employed to develop SARS-CoV-2 vaccines, including the inactivated SARS-CoV-2 particles, mRNA to express viral spike protein, recombinant spike proteins, and viral vectors. Here, we report the use of the vaccinia virus Tiantan strain as a vector to express the SARS-CoV-2 spike protein. When it was used to inoculate mice, robust SARS-CoV-2 spike protein-specific antibody response and T-cell response were detected. Sera from the vaccinated mice showed strong neutralizing activity against the ancestral Wuhan SARS-CoV-2, the variants of concern (VOCs) B.1.351, B.1.617.2, and the emerging B.1.1.529 (omicron). This finding supports the possibility of developing a new type of SARS-CoV-2 vaccine using the vaccinia virus vector. Frontiers Media S.A. 2022-07-22 /pmc/articles/PMC9353262/ /pubmed/35935962 http://dx.doi.org/10.3389/fimmu.2022.911164 Text en Copyright © 2022 Mei, Fan, Liu, Zhao, Huang, Wei, Hu, Xie, Wang, Ai, Liang, Xu and Guo 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 Mei, Shan Fan, Zhangling Liu, Xiaoman Zhao, Fei Huang, Yu Wei, Liang Hu, Yamei Xie, Yu Wang, Liming Ai, Bin Liang, Chen Xu, Fengwen Guo, Fei Immunogenicity of a vaccinia virus-based severe acute respiratory syndrome coronavirus 2 vaccine candidate |
title | Immunogenicity of a vaccinia virus-based severe acute respiratory syndrome coronavirus 2 vaccine candidate |
title_full | Immunogenicity of a vaccinia virus-based severe acute respiratory syndrome coronavirus 2 vaccine candidate |
title_fullStr | Immunogenicity of a vaccinia virus-based severe acute respiratory syndrome coronavirus 2 vaccine candidate |
title_full_unstemmed | Immunogenicity of a vaccinia virus-based severe acute respiratory syndrome coronavirus 2 vaccine candidate |
title_short | Immunogenicity of a vaccinia virus-based severe acute respiratory syndrome coronavirus 2 vaccine candidate |
title_sort | immunogenicity of a vaccinia virus-based severe acute respiratory syndrome coronavirus 2 vaccine candidate |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353262/ https://www.ncbi.nlm.nih.gov/pubmed/35935962 http://dx.doi.org/10.3389/fimmu.2022.911164 |
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