Anti-inflammatory and immunomodulatory mechanisms of artemisinin on contact hypersensitivity

被引:87
作者
Li, Tan [2 ,3 ]
Chen, Hong [1 ,3 ]
Wei, Na [1 ]
Mei, Xin [1 ]
Zhang, Shi [1 ]
Liu, Dai-lin [1 ]
Gao, Ying [1 ]
Bai, Shu-fang [1 ]
Liu, Xiao-guang [1 ]
Zhou, Ya-xun [1 ]
机构
[1] Chinese Peoples Armed Police Force, Dept Pharmacognosy, Coll Med, Tianjin, Peoples R China
[2] Chinese Peoples Armed Police Force, Dept Immunol, Coll Med, Tianjin, Peoples R China
[3] Chinese Peoples Armed Police Force, Tianjin Key Lab Biomarkers Occupat & Environm Haz, Coll Med, Tianjin, Peoples R China
基金
中国博士后科学基金;
关键词
Artemisinin; Immunoregulation; Contact hypersensitivity; Tregs; Th17; REGULATORY T-CELLS; TGF-BETA; P38; DIFFERENTIATION; IL-17; DERIVATIVES; ACTIVATION; TOLERANCE; RESPONSES; CD4(+);
D O I
10.1016/j.intimp.2011.11.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Artemisinin (Art) is a sesquiterpene trioxane lactone from Artemisia annua L., which has been shown to affect immune responses. However, the underlying mechanism remains elusive. In this study, we examined the anti-inflammatory and immunomodulatory effects of Art in a mouse model of contact hypersensitivity (CHS), a T-cell-mediated cutaneous inflammatory reaction. The data showed that topical administration of Art could suppress CHS response and Con A-induced T cell proliferation effectively. Further experiments indicated that Art induced the generation of regulatory T cells (Tregs) and impaired the phosphorylation of AKT, associated with the up-regulation of p38 MAPK activation. Moreover. Art also exerted a strikingly inhibitory effect on IL-17 production, and diminished the level of IL-6 paralleled with an enhancement of TGF-beta, which effects were coupled with a significant reduction of STAT3 activation. These data reveal that Art could effectively block CHS response in mice by inducing the generation of Tregs and suppressing the development of Th17, indicating the potential of Art to be applied as an effective therapeutic agent for treating immune-related diseases. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:144 / 150
页数:7
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