先天性淋巴细胞
白细胞介素33
过敏性炎症
免疫学
炎症
细胞因子
免疫系统
先天免疫系统
医学
肿瘤坏死因子α
生物
白细胞介素
作者
Ben Chung-Lap Chan,Christopher Wai Kei Lam,Lai‐Shan Tam,Chun Kwok Wong
标识
DOI:10.3389/fimmu.2019.00364
摘要
Interleukin (IL)-33 belongs to IL-1 cytokine family which is constitutively produced from the structural and lining cells including fibroblasts, endothelial cells, and epithelial cells of skin, gastrointestinal tract, and lungs that are exposed to the environment. Different from most cytokines that are actively secreted from cells, nuclear cytokine IL-33 is passively released during cell necrosis or when tissues are damaged, suggesting that it may function as an alarmin that alerts the immune system after endothelial or epithelial cell damage during infection, physical stress, or trauma. IL-33 plays important roles in type-2 innate immunity via activation of allergic inflammation-related eosinophils, basophils, mast cells, macrophages, and group 2 innate lymphoid cells (ILC2s) through its receptor ST2. In this review, we focus on the recent advances of the underlying intercellular and intracellular mechanisms by which IL-33 can regulate the allergic inflammation in various allergic diseases including allergic asthma and atopic dermatitis. The future pharmacological strategy and application of traditional Chinese medicines targeting the IL-33/ST2 axis for anti-inflammatory therapy of allergic diseases were also discussed.
科研通智能强力驱动
Strongly Powered by AbleSci AI