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Methionine enkephalin(MENK) upregulated memory T cells in anti-influenza response
Novel prophylactic drugs and vaccination strategies for protection against influenza virus should induce specific effector T-cell immune responses in pulmonary airways and peripheral lymphoid organs. Designing approaches that promote T-cell-mediated responses and memory T-cell differentiation would...
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/PMC10571428/ https://www.ncbi.nlm.nih.gov/pubmed/37828468 http://dx.doi.org/10.1186/s12865-023-00573-0 |
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author | Tian, Jing Fu, Wenrui Xie, Zifeng Wang, Xiaonan Miao, Miao Shan, Fengping Yu, Xiaodong |
author_facet | Tian, Jing Fu, Wenrui Xie, Zifeng Wang, Xiaonan Miao, Miao Shan, Fengping Yu, Xiaodong |
author_sort | Tian, Jing |
collection | PubMed |
description | Novel prophylactic drugs and vaccination strategies for protection against influenza virus should induce specific effector T-cell immune responses in pulmonary airways and peripheral lymphoid organs. Designing approaches that promote T-cell-mediated responses and memory T-cell differentiation would strengthen host resistance to respiratory infectious diseases. The results of this study showed that pulmonary delivery of MENK via intranasal administration reduced viral titres, upregulated opioid receptor MOR and DOR, increased the proportions of T-cell subsets including CD8(+) T cells, CD8(+) T(EM) cells, NP/PA-effector CD8(+) T(EM) cells in bronchoalveolar lavage fluid and lungs, and CD4(+)/CD8(+) T(CM) cells in lymph nodes to protect mice against influenza viral challenge. Furthermore, we demonstrated that, on the 10th day of infection, the proportions of CD4(+) T(M) and CD8(+) T(M) cells were significantly increased, which meant that a stable T(CM) and T(EM) lineage was established in the early stage of influenza infection. Collectively, our data suggested that MENK administered intranasally, similar to the route of natural infection by influenza A virus, could exert antiviral activity through upregulating T-cell-mediated adaptive immune responses against influenza virus. |
format | Online Article Text |
id | pubmed-10571428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105714282023-10-14 Methionine enkephalin(MENK) upregulated memory T cells in anti-influenza response Tian, Jing Fu, Wenrui Xie, Zifeng Wang, Xiaonan Miao, Miao Shan, Fengping Yu, Xiaodong BMC Immunol Research Novel prophylactic drugs and vaccination strategies for protection against influenza virus should induce specific effector T-cell immune responses in pulmonary airways and peripheral lymphoid organs. Designing approaches that promote T-cell-mediated responses and memory T-cell differentiation would strengthen host resistance to respiratory infectious diseases. The results of this study showed that pulmonary delivery of MENK via intranasal administration reduced viral titres, upregulated opioid receptor MOR and DOR, increased the proportions of T-cell subsets including CD8(+) T cells, CD8(+) T(EM) cells, NP/PA-effector CD8(+) T(EM) cells in bronchoalveolar lavage fluid and lungs, and CD4(+)/CD8(+) T(CM) cells in lymph nodes to protect mice against influenza viral challenge. Furthermore, we demonstrated that, on the 10th day of infection, the proportions of CD4(+) T(M) and CD8(+) T(M) cells were significantly increased, which meant that a stable T(CM) and T(EM) lineage was established in the early stage of influenza infection. Collectively, our data suggested that MENK administered intranasally, similar to the route of natural infection by influenza A virus, could exert antiviral activity through upregulating T-cell-mediated adaptive immune responses against influenza virus. BioMed Central 2023-10-12 /pmc/articles/PMC10571428/ /pubmed/37828468 http://dx.doi.org/10.1186/s12865-023-00573-0 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 Tian, Jing Fu, Wenrui Xie, Zifeng Wang, Xiaonan Miao, Miao Shan, Fengping Yu, Xiaodong Methionine enkephalin(MENK) upregulated memory T cells in anti-influenza response |
title | Methionine enkephalin(MENK) upregulated memory T cells in anti-influenza response |
title_full | Methionine enkephalin(MENK) upregulated memory T cells in anti-influenza response |
title_fullStr | Methionine enkephalin(MENK) upregulated memory T cells in anti-influenza response |
title_full_unstemmed | Methionine enkephalin(MENK) upregulated memory T cells in anti-influenza response |
title_short | Methionine enkephalin(MENK) upregulated memory T cells in anti-influenza response |
title_sort | methionine enkephalin(menk) upregulated memory t cells in anti-influenza response |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10571428/ https://www.ncbi.nlm.nih.gov/pubmed/37828468 http://dx.doi.org/10.1186/s12865-023-00573-0 |
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