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Cross-reactive immune responses to monkeypox virus induced by MVA vaccination in mice
Mpox (monkeypox) infection cases increased recently in non-Mpox outbreak areas, potentially causing an international threat. The desire to defend against a potential outbreak has led to renewed efforts to develop Mpox vaccines. In this report, mice were immunized with various doses of modified vacci...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10278293/ https://www.ncbi.nlm.nih.gov/pubmed/37337226 http://dx.doi.org/10.1186/s12985-023-02085-0 |
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author | Gao, Feixia He, Cheng Liu, Min Yuan, Ping Tian, Shihua Zheng, Mei Zhang, Linya Zhou, Xu Xu, Fangjingwei Luo, Jian Li, Xiuling |
author_facet | Gao, Feixia He, Cheng Liu, Min Yuan, Ping Tian, Shihua Zheng, Mei Zhang, Linya Zhou, Xu Xu, Fangjingwei Luo, Jian Li, Xiuling |
author_sort | Gao, Feixia |
collection | PubMed |
description | Mpox (monkeypox) infection cases increased recently in non-Mpox outbreak areas, potentially causing an international threat. The desire to defend against a potential outbreak has led to renewed efforts to develop Mpox vaccines. In this report, mice were immunized with various doses of modified vaccinia virus Ankara (MVA) to evaluate the cross-reactive immune response of MVA immunization against protective antigens of the current monkeypox virus. We demonstrated that MVA induced specific antibodies against protective antigens (A29, A35, B6, M1, H3, and I1), mediating the neutralization abilities against the MVA and the monkeypox virus (MPXV). Moreover, recombinant protective antigens of the MPXV elicited cross-binding and cross-neutralizing activities for MVA. Hence, the MVA induced cross-reactive immune responses, which may guide future efforts to develop vaccines against the recent MPXV. Notably, compared to the other protective antigens, the predominant A29 and M1 antigens mediated higher cross-neutralizing immune responses against the MVA, which could serve as antigen targets for novel orthologous orthopoxvirus vaccine. |
format | Online Article Text |
id | pubmed-10278293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102782932023-06-20 Cross-reactive immune responses to monkeypox virus induced by MVA vaccination in mice Gao, Feixia He, Cheng Liu, Min Yuan, Ping Tian, Shihua Zheng, Mei Zhang, Linya Zhou, Xu Xu, Fangjingwei Luo, Jian Li, Xiuling Virol J Research Mpox (monkeypox) infection cases increased recently in non-Mpox outbreak areas, potentially causing an international threat. The desire to defend against a potential outbreak has led to renewed efforts to develop Mpox vaccines. In this report, mice were immunized with various doses of modified vaccinia virus Ankara (MVA) to evaluate the cross-reactive immune response of MVA immunization against protective antigens of the current monkeypox virus. We demonstrated that MVA induced specific antibodies against protective antigens (A29, A35, B6, M1, H3, and I1), mediating the neutralization abilities against the MVA and the monkeypox virus (MPXV). Moreover, recombinant protective antigens of the MPXV elicited cross-binding and cross-neutralizing activities for MVA. Hence, the MVA induced cross-reactive immune responses, which may guide future efforts to develop vaccines against the recent MPXV. Notably, compared to the other protective antigens, the predominant A29 and M1 antigens mediated higher cross-neutralizing immune responses against the MVA, which could serve as antigen targets for novel orthologous orthopoxvirus vaccine. BioMed Central 2023-06-19 /pmc/articles/PMC10278293/ /pubmed/37337226 http://dx.doi.org/10.1186/s12985-023-02085-0 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Gao, Feixia He, Cheng Liu, Min Yuan, Ping Tian, Shihua Zheng, Mei Zhang, Linya Zhou, Xu Xu, Fangjingwei Luo, Jian Li, Xiuling Cross-reactive immune responses to monkeypox virus induced by MVA vaccination in mice |
title | Cross-reactive immune responses to monkeypox virus induced by MVA vaccination in mice |
title_full | Cross-reactive immune responses to monkeypox virus induced by MVA vaccination in mice |
title_fullStr | Cross-reactive immune responses to monkeypox virus induced by MVA vaccination in mice |
title_full_unstemmed | Cross-reactive immune responses to monkeypox virus induced by MVA vaccination in mice |
title_short | Cross-reactive immune responses to monkeypox virus induced by MVA vaccination in mice |
title_sort | cross-reactive immune responses to monkeypox virus induced by mva vaccination in mice |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10278293/ https://www.ncbi.nlm.nih.gov/pubmed/37337226 http://dx.doi.org/10.1186/s12985-023-02085-0 |
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