IL-33 and Airway Inflammation

被引:77
作者
Oboki, Keisuke
Nakae, Susumu [2 ]
Matsumoto, Kenji
Saito, Hirohisa [1 ]
机构
[1] Natl Res Inst Child Hlth & Dev, Dept Allergy & Immunol, Setagaya Ku, Tokyo 1578535, Japan
[2] Univ Tokyo, Inst Med Sci, Frontier Res Initiat, Tokyo, Japan
关键词
IL-33; ST2; host defense; allergy; autoimmunity; chronic disease; mast cell; basophil; eosinophil; CD4(+) T-CELLS; TH2; CELLS; CYTOKINE PRODUCTION; SOLUBLE ST2; T1/ST2; EXPRESSION; IMMUNE-RESPONSES; HUMAN BASOPHILS; MURINE MODEL; MAST-CELLS; ASTHMA;
D O I
10.4168/aair.2011.3.2.81
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Interleukin-33 (IL-33) is the 11th member of IL-1 cytokine family which includes IL-1 and IL-18. Unlike IL-1 beta and IL-18, IL-33 is suggested to function as an alarmin that is released upon endothelial or epithelial cell damage and may not enhance acquired immune responses through activation of inflammasome. ST2, a IL-33 receptor component, is preferentially expressed by T-helper type (Th) 2 cells, mast cells, eosinophils and basophils, compared to Th1 cells, Th17 cells and neutrophils. Thus, IL-33 profoundly enhances allergic inflammation through increased expression of proallergic cytokines and chemokines. Indeed, IL-33 and its receptor genes are recognized as the most susceptible genes for asthma by several recent genomewide association studies. It has also recently been shown that IL-33 plays a crucial role in innate eosinophilic airway inflammation rather than acquired immune responses such as IgE production. As such, IL-33 provides a unique therapeutic way for asthma, i.e., ameliorating innate airway inflammation.
引用
收藏
页码:81 / 88
页数:8
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