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Recombinant proteins A29L, M1R, A35R, and B6R vaccination protects mice from mpox virus challenge
Since May 2022, mutant strains of mpox (formerly monkeypox) virus (MPXV) have been rapidly spreading among individuals who have not traveled to endemic areas in multiple locations, including Europe and the United States. Both intracellular and extracellular forms of mpox virus have multiple outer me...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10331816/ https://www.ncbi.nlm.nih.gov/pubmed/37435062 http://dx.doi.org/10.3389/fimmu.2023.1203410 |
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author | Tang, Ding Liu, Xiaoke Lu, Jia Fan, Huifen Xu, Xiuli Sun, Kaili Wang, Ruyu Li, Chunyang Dan, Demiao Du, Hongqiao Wang, Zejun Li, Xinguo Yang, Xiaoming |
author_facet | Tang, Ding Liu, Xiaoke Lu, Jia Fan, Huifen Xu, Xiuli Sun, Kaili Wang, Ruyu Li, Chunyang Dan, Demiao Du, Hongqiao Wang, Zejun Li, Xinguo Yang, Xiaoming |
author_sort | Tang, Ding |
collection | PubMed |
description | Since May 2022, mutant strains of mpox (formerly monkeypox) virus (MPXV) have been rapidly spreading among individuals who have not traveled to endemic areas in multiple locations, including Europe and the United States. Both intracellular and extracellular forms of mpox virus have multiple outer membrane proteins that can stimulate immune response. Here, we investigated the immunogenicity of MPXV structural proteins such as A29L, M1R, A35R, and B6R as a combination vaccine, and the protective effect against the 2022 mpox mutant strain was also evaluated in BALB/c mice. After mixed 15 μg QS-21 adjuvant, all four virus structural proteins were administered subcutaneously to mice. Antibody titers in mouse sera rose sharply after the initial boost, along with an increased capacity of immune cells to produce IFN-γ alongside an elevated level of cellular immunity mediated by Th1 cells. The vaccine-induced neutralizing antibodies significantly inhibited the replication of MPXV in mice and reduced the pathological damage of organs. This study demonstrates the feasibility of a multiple recombinant vaccine for MPXV variant strains. |
format | Online Article Text |
id | pubmed-10331816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103318162023-07-11 Recombinant proteins A29L, M1R, A35R, and B6R vaccination protects mice from mpox virus challenge Tang, Ding Liu, Xiaoke Lu, Jia Fan, Huifen Xu, Xiuli Sun, Kaili Wang, Ruyu Li, Chunyang Dan, Demiao Du, Hongqiao Wang, Zejun Li, Xinguo Yang, Xiaoming Front Immunol Immunology Since May 2022, mutant strains of mpox (formerly monkeypox) virus (MPXV) have been rapidly spreading among individuals who have not traveled to endemic areas in multiple locations, including Europe and the United States. Both intracellular and extracellular forms of mpox virus have multiple outer membrane proteins that can stimulate immune response. Here, we investigated the immunogenicity of MPXV structural proteins such as A29L, M1R, A35R, and B6R as a combination vaccine, and the protective effect against the 2022 mpox mutant strain was also evaluated in BALB/c mice. After mixed 15 μg QS-21 adjuvant, all four virus structural proteins were administered subcutaneously to mice. Antibody titers in mouse sera rose sharply after the initial boost, along with an increased capacity of immune cells to produce IFN-γ alongside an elevated level of cellular immunity mediated by Th1 cells. The vaccine-induced neutralizing antibodies significantly inhibited the replication of MPXV in mice and reduced the pathological damage of organs. This study demonstrates the feasibility of a multiple recombinant vaccine for MPXV variant strains. Frontiers Media S.A. 2023-06-26 /pmc/articles/PMC10331816/ /pubmed/37435062 http://dx.doi.org/10.3389/fimmu.2023.1203410 Text en Copyright © 2023 Tang, Liu, Lu, Fan, Xu, Sun, Wang, Li, Dan, Du, Wang, Li and Yang 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 Tang, Ding Liu, Xiaoke Lu, Jia Fan, Huifen Xu, Xiuli Sun, Kaili Wang, Ruyu Li, Chunyang Dan, Demiao Du, Hongqiao Wang, Zejun Li, Xinguo Yang, Xiaoming Recombinant proteins A29L, M1R, A35R, and B6R vaccination protects mice from mpox virus challenge |
title | Recombinant proteins A29L, M1R, A35R, and B6R vaccination protects mice from mpox virus challenge |
title_full | Recombinant proteins A29L, M1R, A35R, and B6R vaccination protects mice from mpox virus challenge |
title_fullStr | Recombinant proteins A29L, M1R, A35R, and B6R vaccination protects mice from mpox virus challenge |
title_full_unstemmed | Recombinant proteins A29L, M1R, A35R, and B6R vaccination protects mice from mpox virus challenge |
title_short | Recombinant proteins A29L, M1R, A35R, and B6R vaccination protects mice from mpox virus challenge |
title_sort | recombinant proteins a29l, m1r, a35r, and b6r vaccination protects mice from mpox virus challenge |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10331816/ https://www.ncbi.nlm.nih.gov/pubmed/37435062 http://dx.doi.org/10.3389/fimmu.2023.1203410 |
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