Low-dose IL-2 therapy invigorates CD8+ T cells for viral control in systemic lupus erythematosus.

Autoimmune diseases are often treated by glucocorticoids and immunosuppressive drugs that could increase the risk for infection, which in turn deteriorate disease and cause mortality. Low-dose IL-2 (Ld-IL2) therapy emerges as a new treatment for a wide range of autoimmune diseases. To examine its in...

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Autores principales: Pengcheng Zhou, Jiali Chen, Jing He, Ting Zheng, Joseph Yunis, Victor Makota, Yannick O Alexandre, Fang Gong, Xia Zhang, Wuxiang Xie, Yuhui Li, Miao Shao, Yanshan Zhu, Jane E Sinclair, Miao Miao, Yaping Chen, Kirsty R Short, Scott N Mueller, Xiaolin Sun, Di Yu, Zhanguo Li
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Publicado: Public Library of Science (PLoS) 2021
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spelling oai:doaj.org-article:6892f12d515d4852b12e973d2e669c972021-12-02T20:00:03ZLow-dose IL-2 therapy invigorates CD8+ T cells for viral control in systemic lupus erythematosus.1553-73661553-737410.1371/journal.ppat.1009858https://doaj.org/article/6892f12d515d4852b12e973d2e669c972021-10-01T00:00:00Zhttps://doi.org/10.1371/journal.ppat.1009858https://doaj.org/toc/1553-7366https://doaj.org/toc/1553-7374Autoimmune diseases are often treated by glucocorticoids and immunosuppressive drugs that could increase the risk for infection, which in turn deteriorate disease and cause mortality. Low-dose IL-2 (Ld-IL2) therapy emerges as a new treatment for a wide range of autoimmune diseases. To examine its influence on infection, we retrospectively studied 665 patients with systemic lupus erythematosus (SLE) including about one third receiving Ld-IL2 therapy, where Ld-IL2 therapy was found beneficial in reducing the incidence of infections. In line with this clinical observation, IL-2 treatment accelerated viral clearance in mice infected with influenza A virus or lymphocytic choriomeningitis virus (LCMV). Noticeably, despite enhancing anti-viral immunity in LCMV infection, IL-2 treatment exacerbated CD8+ T cell-mediated immunopathology. In summary, Ld-IL2 therapy reduced the risk of infections in SLE patients and enhanced the control of viral infection, but caution should be taken to avoid potential CD8+ T cell-mediated immunopathology.Pengcheng ZhouJiali ChenJing HeTing ZhengJoseph YunisVictor MakotaYannick O AlexandreFang GongXia ZhangWuxiang XieYuhui LiMiao ShaoYanshan ZhuJane E SinclairMiao MiaoYaping ChenKirsty R ShortScott N MuellerXiaolin SunDi YuZhanguo LiPublic Library of Science (PLoS)articleImmunologic diseases. AllergyRC581-607Biology (General)QH301-705.5ENPLoS Pathogens, Vol 17, Iss 10, p e1009858 (2021)
institution DOAJ
collection DOAJ
language EN
topic Immunologic diseases. Allergy
RC581-607
Biology (General)
QH301-705.5
spellingShingle Immunologic diseases. Allergy
RC581-607
Biology (General)
QH301-705.5
Pengcheng Zhou
Jiali Chen
Jing He
Ting Zheng
Joseph Yunis
Victor Makota
Yannick O Alexandre
Fang Gong
Xia Zhang
Wuxiang Xie
Yuhui Li
Miao Shao
Yanshan Zhu
Jane E Sinclair
Miao Miao
Yaping Chen
Kirsty R Short
Scott N Mueller
Xiaolin Sun
Di Yu
Zhanguo Li
Low-dose IL-2 therapy invigorates CD8+ T cells for viral control in systemic lupus erythematosus.
description Autoimmune diseases are often treated by glucocorticoids and immunosuppressive drugs that could increase the risk for infection, which in turn deteriorate disease and cause mortality. Low-dose IL-2 (Ld-IL2) therapy emerges as a new treatment for a wide range of autoimmune diseases. To examine its influence on infection, we retrospectively studied 665 patients with systemic lupus erythematosus (SLE) including about one third receiving Ld-IL2 therapy, where Ld-IL2 therapy was found beneficial in reducing the incidence of infections. In line with this clinical observation, IL-2 treatment accelerated viral clearance in mice infected with influenza A virus or lymphocytic choriomeningitis virus (LCMV). Noticeably, despite enhancing anti-viral immunity in LCMV infection, IL-2 treatment exacerbated CD8+ T cell-mediated immunopathology. In summary, Ld-IL2 therapy reduced the risk of infections in SLE patients and enhanced the control of viral infection, but caution should be taken to avoid potential CD8+ T cell-mediated immunopathology.
format article
author Pengcheng Zhou
Jiali Chen
Jing He
Ting Zheng
Joseph Yunis
Victor Makota
Yannick O Alexandre
Fang Gong
Xia Zhang
Wuxiang Xie
Yuhui Li
Miao Shao
Yanshan Zhu
Jane E Sinclair
Miao Miao
Yaping Chen
Kirsty R Short
Scott N Mueller
Xiaolin Sun
Di Yu
Zhanguo Li
author_facet Pengcheng Zhou
Jiali Chen
Jing He
Ting Zheng
Joseph Yunis
Victor Makota
Yannick O Alexandre
Fang Gong
Xia Zhang
Wuxiang Xie
Yuhui Li
Miao Shao
Yanshan Zhu
Jane E Sinclair
Miao Miao
Yaping Chen
Kirsty R Short
Scott N Mueller
Xiaolin Sun
Di Yu
Zhanguo Li
author_sort Pengcheng Zhou
title Low-dose IL-2 therapy invigorates CD8+ T cells for viral control in systemic lupus erythematosus.
title_short Low-dose IL-2 therapy invigorates CD8+ T cells for viral control in systemic lupus erythematosus.
title_full Low-dose IL-2 therapy invigorates CD8+ T cells for viral control in systemic lupus erythematosus.
title_fullStr Low-dose IL-2 therapy invigorates CD8+ T cells for viral control in systemic lupus erythematosus.
title_full_unstemmed Low-dose IL-2 therapy invigorates CD8+ T cells for viral control in systemic lupus erythematosus.
title_sort low-dose il-2 therapy invigorates cd8+ t cells for viral control in systemic lupus erythematosus.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/6892f12d515d4852b12e973d2e669c97
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