Interleukin-33 in Tissue Homeostasis, Injury, and Inflammation

被引:261
作者
Molofsky, Ari B. [3 ,4 ]
Savage, Adam K. [1 ,3 ]
Locksley, Richard M. [1 ,2 ,3 ]
机构
[1] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Lab Med, San Francisco, CA 94143 USA
关键词
INNATE LYMPHOID-CELLS; REGULATORY T-CELLS; THYMIC STROMAL LYMPHOPOIETIN; VISCERAL ADIPOSE-TISSUE; RECEPTOR FAMILY-MEMBER; TYPE-2; IMMUNITY; CYTOKINE IL-33; ALARMIN IL-33; ST2; PROTEIN; CD8(+) T;
D O I
10.1016/j.immuni.2015.06.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interleukin-33 (IL-33) is a nuclear-associated cytokine of the IL-1 family originally described as a potent inducer of allergic type 2 immunity. IL-33 signals via the receptor ST2, which is highly expressed on group 2 innate lymphoid cells (ILC2s) and T helper 2 (Th2) cells, thus underpinning its association with helminth infection and allergic pathology. Recent studies have revealed ST2 expression on subsets of regulatory T cells, and for a role for IL-33 in tissue homeostasis and repair that suggests previously unrecognized interactions within these cellular networks. IL-33 can participate in pathologic fibrotic reactions, or, in the setting of microbial invasion, can cooperate with inflammatory cytokines to promote responses by cytotoxic NK cells, Th1 cells, and CD8(+) T cells. Here, we highlight the regulation and function of IL-33 and ST2 and review their roles in homeostasis, damage, and inflammation, suggesting a conceptual framework for future studies.
引用
收藏
页码:1005 / 1019
页数:15
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