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VLPs containing stalk domain and ectodomain of matrix protein 2 of influenza induce protection in mice

BACKGROUND: As a result of antigenic drift, current influenza vaccines provide limited protection against circulating influenza viruses, and vaccines with broad cross protection are urgently needed. Hemagglutinin stalk domain and ectodomain of matrix protein 2 are highly conserved among influenza vi...

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Autores principales: Shi, Lili, Long, Ying, Zhu, Yanyan, Dong, Jingjian, Chen, Yan, Feng, Hao, Sun, Xianliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972598/
https://www.ncbi.nlm.nih.gov/pubmed/36849974
http://dx.doi.org/10.1186/s12985-023-01994-4
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author Shi, Lili
Long, Ying
Zhu, Yanyan
Dong, Jingjian
Chen, Yan
Feng, Hao
Sun, Xianliang
author_facet Shi, Lili
Long, Ying
Zhu, Yanyan
Dong, Jingjian
Chen, Yan
Feng, Hao
Sun, Xianliang
author_sort Shi, Lili
collection PubMed
description BACKGROUND: As a result of antigenic drift, current influenza vaccines provide limited protection against circulating influenza viruses, and vaccines with broad cross protection are urgently needed. Hemagglutinin stalk domain and ectodomain of matrix protein 2 are highly conserved among influenza viruses and have great potential for use as a universal vaccine. METHODS: In this study, we co-expressed the stalk domain and M2e on the surface of cell membranes and generated chimeric and standard virus-like particles of influenza to improve antigen immunogenicity. We subsequently immunized BALB/c mice through intranasal and intramuscular routes. RESULTS: Data obtained demonstrated that vaccination with VLPs elicited high levels of serum-specific IgG (approximately 30-fold higher than that obtained with soluble protein), induced increased ADCC activity to the influenza virus, and enhanced T cell as well as mucosal immune responses. Furthermore, mice immunized by VLP had elevated level of mucosal HA and 4M2e specific IgA titers and cytokine production as compared to mice immunized with soluble protein. Additionally, the VLP-immunized group exhibited long-lasting humoral antibody responses and effectively reduced lung viral titers after the challenge. Compared to the 4M2e-VLP and mHA-VLP groups, the chimeric VLP group experienced cross-protection against the lethal challenge with homologous and heterologous viruses. The stalk domain specific antibody conferred better protection than the 4M2e specific antibody. CONCLUSION: Our findings demonstrated that the chimeric VLPs anchored with the stalk domain and M2e showed efficacy in reducing viral loads after the influenza virus challenge in the mice model. This antibody can be used in humans to broadly protect against a variety of influenza virus subtypes. The chimeric VLPs represent a novel approach to increase antigen immunogenicity and are promising candidates for a universal influenza vaccine.
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spelling pubmed-99725982023-03-01 VLPs containing stalk domain and ectodomain of matrix protein 2 of influenza induce protection in mice Shi, Lili Long, Ying Zhu, Yanyan Dong, Jingjian Chen, Yan Feng, Hao Sun, Xianliang Virol J Research BACKGROUND: As a result of antigenic drift, current influenza vaccines provide limited protection against circulating influenza viruses, and vaccines with broad cross protection are urgently needed. Hemagglutinin stalk domain and ectodomain of matrix protein 2 are highly conserved among influenza viruses and have great potential for use as a universal vaccine. METHODS: In this study, we co-expressed the stalk domain and M2e on the surface of cell membranes and generated chimeric and standard virus-like particles of influenza to improve antigen immunogenicity. We subsequently immunized BALB/c mice through intranasal and intramuscular routes. RESULTS: Data obtained demonstrated that vaccination with VLPs elicited high levels of serum-specific IgG (approximately 30-fold higher than that obtained with soluble protein), induced increased ADCC activity to the influenza virus, and enhanced T cell as well as mucosal immune responses. Furthermore, mice immunized by VLP had elevated level of mucosal HA and 4M2e specific IgA titers and cytokine production as compared to mice immunized with soluble protein. Additionally, the VLP-immunized group exhibited long-lasting humoral antibody responses and effectively reduced lung viral titers after the challenge. Compared to the 4M2e-VLP and mHA-VLP groups, the chimeric VLP group experienced cross-protection against the lethal challenge with homologous and heterologous viruses. The stalk domain specific antibody conferred better protection than the 4M2e specific antibody. CONCLUSION: Our findings demonstrated that the chimeric VLPs anchored with the stalk domain and M2e showed efficacy in reducing viral loads after the influenza virus challenge in the mice model. This antibody can be used in humans to broadly protect against a variety of influenza virus subtypes. The chimeric VLPs represent a novel approach to increase antigen immunogenicity and are promising candidates for a universal influenza vaccine. BioMed Central 2023-02-27 /pmc/articles/PMC9972598/ /pubmed/36849974 http://dx.doi.org/10.1186/s12985-023-01994-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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
Shi, Lili
Long, Ying
Zhu, Yanyan
Dong, Jingjian
Chen, Yan
Feng, Hao
Sun, Xianliang
VLPs containing stalk domain and ectodomain of matrix protein 2 of influenza induce protection in mice
title VLPs containing stalk domain and ectodomain of matrix protein 2 of influenza induce protection in mice
title_full VLPs containing stalk domain and ectodomain of matrix protein 2 of influenza induce protection in mice
title_fullStr VLPs containing stalk domain and ectodomain of matrix protein 2 of influenza induce protection in mice
title_full_unstemmed VLPs containing stalk domain and ectodomain of matrix protein 2 of influenza induce protection in mice
title_short VLPs containing stalk domain and ectodomain of matrix protein 2 of influenza induce protection in mice
title_sort vlps containing stalk domain and ectodomain of matrix protein 2 of influenza induce protection in mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972598/
https://www.ncbi.nlm.nih.gov/pubmed/36849974
http://dx.doi.org/10.1186/s12985-023-01994-4
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