Strategies targeting IL-33/ST2 axis in the treatment of allergic diseases

被引:3
作者
Li, Wenran [1 ]
Liu, Mengqi [1 ]
Chu, Ming [1 ,2 ]
机构
[1] Peking Univ, Hlth Sci Ctr, Sch Basic Med Sci, Dept Immunol, Beijing, Peoples R China
[2] Beijing Life Sci Acad, Beijing, Peoples R China
关键词
IL-33; ST2; MyD88/IRAK/TRAF6; Allergic diseases; MAST-CELL CHYMASE; NF-KAPPA-B; INNATE LYMPHOID-CELLS; ST2; GENE-PRODUCT; AIRWAY INFLAMMATION; INTERLEUKIN-33; PRODUCTION; NLRP3; INFLAMMASOME; SOLUBLE ST2; EPITHELIAL-CELLS; VARIANT FORM;
D O I
10.1016/j.bcp.2023.115911
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Interleukin-33 (IL-33) and its receptor Serum Stimulation-2 (ST2, also called Il1rl1) are members of the IL-1 superfamily that plays a crucial role in allergic diseases. The interaction of IL-33 and ST2 mainly activates NF-kappa B signaling and MAPK signaling via the MyD88/IRAK/TRAF6 module, resulting in the production and secretion of pro-inflammatory cytokines. The IL-33/ST2 axis participates in the pathogenesis of allergic diseases, and therefore serves as a promising strategy for allergy treatment. In recent years, strategies blocking IL-33/ST2 through targeting regulation of IL-33 and ST2 or targeting the molecules involved in the signal transduction have been extensively studied mostly in animal models. These studies provide various potential therapeutic agents other than antibodies, such as small molecules, nucleic acids and traditional Chinese medicines. Herein, we reviewed potential targets and agents targeting IL-33/ST2 axis in the treatment of allergic diseases, providing directions for further investigations on treatments for IL-33 induced allergic diseases.
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页数:17
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