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Interleukin‐33 ( IL ‐33): A nuclear cytokine from the IL ‐1 family
Author(s) -
Cayrol Corinne,
Girard JeanPhilippe
Publication year - 2018
Publication title -
immunological reviews
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.839
H-Index - 223
eISSN - 1600-065X
pISSN - 0105-2896
DOI - 10.1111/imr.12619
Subject(s) - interleukin 33 , innate lymphoid cell , biology , immune system , immunology , cytokine , microbiology and biotechnology , allergic inflammation , inflammation , il 2 receptor , interleukin 12 , interleukin 21 , innate immune system , cd8 , cytotoxic t cell , interleukin , t cell , in vitro , biochemistry
Summary Interleukin‐33 ( IL ‐33) is a tissue‐derived nuclear cytokine from the IL ‐1 family abundantly expressed in endothelial cells, epithelial cells and fibroblast‐like cells, both during homeostasis and inflammation. It functions as an alarm signal (alarmin) released upon cell injury or tissue damage to alert immune cells expressing the ST 2 receptor ( IL ‐1 RL 1). The major targets of IL ‐33 in vivo are tissue‐resident immune cells such as mast cells, group 2 innate lymphoid cells ( ILC 2s) and regulatory T cells (Tregs). Other cellular targets include T helper 2 (Th2) cells, eosinophils, basophils, dendritic cells, Th1 cells, CD 8 + T cells, NK cells, iNKT cells, B cells, neutrophils and macrophages. IL ‐33 is thus emerging as a crucial immune modulator with pleiotropic activities in type‐2, type‐1 and regulatory immune responses, and important roles in allergic, fibrotic, infectious, and chronic inflammatory diseases. The critical function of IL ‐33/ ST 2 signaling in allergic inflammation is illustrated by the fact that IL 33 and IL 1 RL 1 are among the most highly replicated susceptibility loci for asthma. In this review, we highlight 15 years of discoveries on IL ‐33 protein, including its molecular characteristics, nuclear localization, bioactive forms, cellular sources, mechanisms of release and regulation by proteases. Importantly, we emphasize data that have been validated using IL ‐33 ‐deficient cells.