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Protective role of follicular CXCR5(+)CD8(+) T cells against dengue virus 2 infection
Follicular CXCR5(+)CD8(+) T cells have antiviral effects in chronic virus infection, but the roles of these cells during dengue virus 2 (DENV2) infection remain poorly understood. OBJECTIVE: This study was conducted to analyzed in detail the dynamic changes and functional properties of circulating f...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7110549/ https://www.ncbi.nlm.nih.gov/pubmed/30904675 http://dx.doi.org/10.1016/j.ijid.2019.03.024 |
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author | Qiu, Liannv Wang, Hong Yu, Qinhua Liu, JieJing Chen, Sufeng Zhao, Zhao |
author_facet | Qiu, Liannv Wang, Hong Yu, Qinhua Liu, JieJing Chen, Sufeng Zhao, Zhao |
author_sort | Qiu, Liannv |
collection | PubMed |
description | Follicular CXCR5(+)CD8(+) T cells have antiviral effects in chronic virus infection, but the roles of these cells during dengue virus 2 (DENV2) infection remain poorly understood. OBJECTIVE: This study was conducted to analyzed in detail the dynamic changes and functional properties of circulating follicular CXCR5(+)CD8(+) T cells to explore their effects on DENV2 infection. METHODS: Circulating follicular CXCR5(+)CD8(+) T cells and cytokines were analyzed by flow cytometry in DENV2 patients at difference days after DENV2 infection. CD8(+) T cells were isolated and purified from DENV2 patients, then were stimulated with NS1 peptides and TCR stimulant. After cultivation, multiple parameters were tested. RESULTS: (1) CXCR5(+)CD8(+) T cells emerged after DENV2 infection, with high PD-1 expression, and were correlated with the reduction in DENV2 RNA viral loads. (2) PD-1(+)CXCR5(+)CD8(+) T cells were negatively associated with disease progression. (3) Serum IFN-γ, IL-6 and IL-10 levels were increased late in the course of DENV2 infection. (4) CXCR5(+)CD8(+) T cells from DENV2 patients exhibited increased cytotoxicity and IFN-γ and IL-10 secretion. CONCLUSION: CXCR5(+)CD8(+) T cells could play a protective role in dengue pathogenesis and may be a novel strategy for controlling DENV2 infection and vaccine development. |
format | Online Article Text |
id | pubmed-7110549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Authors. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71105492020-04-02 Protective role of follicular CXCR5(+)CD8(+) T cells against dengue virus 2 infection Qiu, Liannv Wang, Hong Yu, Qinhua Liu, JieJing Chen, Sufeng Zhao, Zhao Int J Infect Dis Article Follicular CXCR5(+)CD8(+) T cells have antiviral effects in chronic virus infection, but the roles of these cells during dengue virus 2 (DENV2) infection remain poorly understood. OBJECTIVE: This study was conducted to analyzed in detail the dynamic changes and functional properties of circulating follicular CXCR5(+)CD8(+) T cells to explore their effects on DENV2 infection. METHODS: Circulating follicular CXCR5(+)CD8(+) T cells and cytokines were analyzed by flow cytometry in DENV2 patients at difference days after DENV2 infection. CD8(+) T cells were isolated and purified from DENV2 patients, then were stimulated with NS1 peptides and TCR stimulant. After cultivation, multiple parameters were tested. RESULTS: (1) CXCR5(+)CD8(+) T cells emerged after DENV2 infection, with high PD-1 expression, and were correlated with the reduction in DENV2 RNA viral loads. (2) PD-1(+)CXCR5(+)CD8(+) T cells were negatively associated with disease progression. (3) Serum IFN-γ, IL-6 and IL-10 levels were increased late in the course of DENV2 infection. (4) CXCR5(+)CD8(+) T cells from DENV2 patients exhibited increased cytotoxicity and IFN-γ and IL-10 secretion. CONCLUSION: CXCR5(+)CD8(+) T cells could play a protective role in dengue pathogenesis and may be a novel strategy for controlling DENV2 infection and vaccine development. The Authors. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. 2019-06 2019-03-20 /pmc/articles/PMC7110549/ /pubmed/30904675 http://dx.doi.org/10.1016/j.ijid.2019.03.024 Text en © 2019 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Qiu, Liannv Wang, Hong Yu, Qinhua Liu, JieJing Chen, Sufeng Zhao, Zhao Protective role of follicular CXCR5(+)CD8(+) T cells against dengue virus 2 infection |
title | Protective role of follicular CXCR5(+)CD8(+) T cells against dengue virus 2 infection |
title_full | Protective role of follicular CXCR5(+)CD8(+) T cells against dengue virus 2 infection |
title_fullStr | Protective role of follicular CXCR5(+)CD8(+) T cells against dengue virus 2 infection |
title_full_unstemmed | Protective role of follicular CXCR5(+)CD8(+) T cells against dengue virus 2 infection |
title_short | Protective role of follicular CXCR5(+)CD8(+) T cells against dengue virus 2 infection |
title_sort | protective role of follicular cxcr5(+)cd8(+) t cells against dengue virus 2 infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7110549/ https://www.ncbi.nlm.nih.gov/pubmed/30904675 http://dx.doi.org/10.1016/j.ijid.2019.03.024 |
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