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HTNV infection of CD8(+) T cells is associated with disease progression in HFRS patients
Hantaan viruses (HTNVs) are zoonotic pathogens transmitted mainly by rodents and capable of infecting humans. Increasing knowledge of the human response to HTNV infection can guide the development of new preventative vaccines and therapeutic strategies. Here, we show that HTNV can infect CD8(+) T ce...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8173013/ https://www.ncbi.nlm.nih.gov/pubmed/34079056 http://dx.doi.org/10.1038/s42003-021-02182-2 |
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author | Liu, Rongrong Ma, Ruixue Liu, Ziyu Hu, Haifeng Shu, Jiayi Hu, Peizhen Kang, Junjun Zhang, Yusi Han, Mingwei Zhang, Xiaoxiao Zheng, Yiting Ying, Qikang Hou, Shiyuan Wang, Wenqiu Wang, Fang Cheng, Ning Zhuang, Yan Lian, Jianqi Jin, Xia Wu, Xingan |
author_facet | Liu, Rongrong Ma, Ruixue Liu, Ziyu Hu, Haifeng Shu, Jiayi Hu, Peizhen Kang, Junjun Zhang, Yusi Han, Mingwei Zhang, Xiaoxiao Zheng, Yiting Ying, Qikang Hou, Shiyuan Wang, Wenqiu Wang, Fang Cheng, Ning Zhuang, Yan Lian, Jianqi Jin, Xia Wu, Xingan |
author_sort | Liu, Rongrong |
collection | PubMed |
description | Hantaan viruses (HTNVs) are zoonotic pathogens transmitted mainly by rodents and capable of infecting humans. Increasing knowledge of the human response to HTNV infection can guide the development of new preventative vaccines and therapeutic strategies. Here, we show that HTNV can infect CD8(+) T cells in vivo in patients diagnosed with hemorrhagic fever with renal syndrome (HFRS). Electron microscopy-mediated tracking of the life cycle and ultrastructure of HTNV-infected CD8(+) T cells in vitro showed an association between notable increases in cytoplasmic multivesicular bodies and virus production. Notably, based on a clinical cohort of 280 patients, we found that circulating HTNV-infected CD8(+) T cell numbers in blood were proportional to disease severity. These results demonstrate that viral infected CD8(+) T cells may be used as an adjunct marker for monitoring HFRS disease progression and that modulating T cell functions may be explored for new treatment strategies. |
format | Online Article Text |
id | pubmed-8173013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81730132021-06-07 HTNV infection of CD8(+) T cells is associated with disease progression in HFRS patients Liu, Rongrong Ma, Ruixue Liu, Ziyu Hu, Haifeng Shu, Jiayi Hu, Peizhen Kang, Junjun Zhang, Yusi Han, Mingwei Zhang, Xiaoxiao Zheng, Yiting Ying, Qikang Hou, Shiyuan Wang, Wenqiu Wang, Fang Cheng, Ning Zhuang, Yan Lian, Jianqi Jin, Xia Wu, Xingan Commun Biol Article Hantaan viruses (HTNVs) are zoonotic pathogens transmitted mainly by rodents and capable of infecting humans. Increasing knowledge of the human response to HTNV infection can guide the development of new preventative vaccines and therapeutic strategies. Here, we show that HTNV can infect CD8(+) T cells in vivo in patients diagnosed with hemorrhagic fever with renal syndrome (HFRS). Electron microscopy-mediated tracking of the life cycle and ultrastructure of HTNV-infected CD8(+) T cells in vitro showed an association between notable increases in cytoplasmic multivesicular bodies and virus production. Notably, based on a clinical cohort of 280 patients, we found that circulating HTNV-infected CD8(+) T cell numbers in blood were proportional to disease severity. These results demonstrate that viral infected CD8(+) T cells may be used as an adjunct marker for monitoring HFRS disease progression and that modulating T cell functions may be explored for new treatment strategies. Nature Publishing Group UK 2021-06-02 /pmc/articles/PMC8173013/ /pubmed/34079056 http://dx.doi.org/10.1038/s42003-021-02182-2 Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Liu, Rongrong Ma, Ruixue Liu, Ziyu Hu, Haifeng Shu, Jiayi Hu, Peizhen Kang, Junjun Zhang, Yusi Han, Mingwei Zhang, Xiaoxiao Zheng, Yiting Ying, Qikang Hou, Shiyuan Wang, Wenqiu Wang, Fang Cheng, Ning Zhuang, Yan Lian, Jianqi Jin, Xia Wu, Xingan HTNV infection of CD8(+) T cells is associated with disease progression in HFRS patients |
title | HTNV infection of CD8(+) T cells is associated with disease progression in HFRS patients |
title_full | HTNV infection of CD8(+) T cells is associated with disease progression in HFRS patients |
title_fullStr | HTNV infection of CD8(+) T cells is associated with disease progression in HFRS patients |
title_full_unstemmed | HTNV infection of CD8(+) T cells is associated with disease progression in HFRS patients |
title_short | HTNV infection of CD8(+) T cells is associated with disease progression in HFRS patients |
title_sort | htnv infection of cd8(+) t cells is associated with disease progression in hfrs patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8173013/ https://www.ncbi.nlm.nih.gov/pubmed/34079056 http://dx.doi.org/10.1038/s42003-021-02182-2 |
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