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CD38(+)CD39(+) NK cells associate with HIV disease progression and negatively regulate T cell proliferation
The ectonucleotidases CD38 and CD39 have a critical regulatory effect on tumors and viral infections via the adenosine axis. Natural killer (NK) cells produce cytokines, induce cytotoxic responses against viral infection, and acquire immunoregulatory properties. However, the roles of CD38 and CD39 e...
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/PMC9577302/ https://www.ncbi.nlm.nih.gov/pubmed/36268017 http://dx.doi.org/10.3389/fimmu.2022.946871 |
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author | Qian, Shi Xiong, Chunbin Wang, Meiting Zhang, Zining Fu, Yajing Hu, Qinghai Ding, Haibo Han, Xiaoxu Shang, Hong Jiang, Yongjun |
author_facet | Qian, Shi Xiong, Chunbin Wang, Meiting Zhang, Zining Fu, Yajing Hu, Qinghai Ding, Haibo Han, Xiaoxu Shang, Hong Jiang, Yongjun |
author_sort | Qian, Shi |
collection | PubMed |
description | The ectonucleotidases CD38 and CD39 have a critical regulatory effect on tumors and viral infections via the adenosine axis. Natural killer (NK) cells produce cytokines, induce cytotoxic responses against viral infection, and acquire immunoregulatory properties. However, the roles of CD38 and CD39 expressed NK cells in HIV disease require elucidation. Our study showed that the proportions of CD38(+)CD39(+) NK cells in HIV-infected individuals were positively associated with HIV viral loads and negatively associated with the CD4(+) T cell count. Furthermore, CD38(+)CD39(+) NK cells expressed additional inhibitory receptors, TIM-3 and LAG-3, and produced more TGF-β. Moreover, autologous NK cells suppressed the proliferation of CD8(+) T and CD4(+) T cells of HIV-infected individuals, and inhibiting CD38 and CD39 on NK cells restored CD8(+) T and CD4(+) T cell proliferation in vitro. In conclusion, these data support a critical role for CD38 and CD39 on NK cells in HIV infection and targeting CD38 and CD39 on NK cells may be a potential therapeutic strategy against HIV infection. |
format | Online Article Text |
id | pubmed-9577302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95773022022-10-19 CD38(+)CD39(+) NK cells associate with HIV disease progression and negatively regulate T cell proliferation Qian, Shi Xiong, Chunbin Wang, Meiting Zhang, Zining Fu, Yajing Hu, Qinghai Ding, Haibo Han, Xiaoxu Shang, Hong Jiang, Yongjun Front Immunol Immunology The ectonucleotidases CD38 and CD39 have a critical regulatory effect on tumors and viral infections via the adenosine axis. Natural killer (NK) cells produce cytokines, induce cytotoxic responses against viral infection, and acquire immunoregulatory properties. However, the roles of CD38 and CD39 expressed NK cells in HIV disease require elucidation. Our study showed that the proportions of CD38(+)CD39(+) NK cells in HIV-infected individuals were positively associated with HIV viral loads and negatively associated with the CD4(+) T cell count. Furthermore, CD38(+)CD39(+) NK cells expressed additional inhibitory receptors, TIM-3 and LAG-3, and produced more TGF-β. Moreover, autologous NK cells suppressed the proliferation of CD8(+) T and CD4(+) T cells of HIV-infected individuals, and inhibiting CD38 and CD39 on NK cells restored CD8(+) T and CD4(+) T cell proliferation in vitro. In conclusion, these data support a critical role for CD38 and CD39 on NK cells in HIV infection and targeting CD38 and CD39 on NK cells may be a potential therapeutic strategy against HIV infection. Frontiers Media S.A. 2022-10-04 /pmc/articles/PMC9577302/ /pubmed/36268017 http://dx.doi.org/10.3389/fimmu.2022.946871 Text en Copyright © 2022 Qian, Xiong, Wang, Zhang, Fu, Hu, Ding, Han, Shang and Jiang 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 Qian, Shi Xiong, Chunbin Wang, Meiting Zhang, Zining Fu, Yajing Hu, Qinghai Ding, Haibo Han, Xiaoxu Shang, Hong Jiang, Yongjun CD38(+)CD39(+) NK cells associate with HIV disease progression and negatively regulate T cell proliferation |
title | CD38(+)CD39(+) NK cells associate with HIV disease progression and negatively regulate T cell proliferation |
title_full | CD38(+)CD39(+) NK cells associate with HIV disease progression and negatively regulate T cell proliferation |
title_fullStr | CD38(+)CD39(+) NK cells associate with HIV disease progression and negatively regulate T cell proliferation |
title_full_unstemmed | CD38(+)CD39(+) NK cells associate with HIV disease progression and negatively regulate T cell proliferation |
title_short | CD38(+)CD39(+) NK cells associate with HIV disease progression and negatively regulate T cell proliferation |
title_sort | cd38(+)cd39(+) nk cells associate with hiv disease progression and negatively regulate t cell proliferation |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9577302/ https://www.ncbi.nlm.nih.gov/pubmed/36268017 http://dx.doi.org/10.3389/fimmu.2022.946871 |
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