免疫学
多发性硬化
银屑病
医学
自身免疫性肝炎
炎症性肠病
自身免疫性疾病
免疫系统
白细胞介素23
自身免疫
微嵌合体
白细胞介素17
疾病
类风湿性关节炎
肝炎
生物
抗体
怀孕
胎儿
病理
遗传学
作者
Lin‐Chong Su,Xiaoyan Liu,An‐Fang Huang,Wang‐Dong Xu
标识
DOI:10.1016/j.autrev.2018.01.017
摘要
Interleukin 35 (IL-35) is the recently identified member of the IL-12 family of cytokines and provides the possibility to be a target for new therapies for autoimmune, inflammatory diseases. It is composed of an α chain (p35) and a β chain (EBI3). IL-35 mediates signaling by binding to its receptors, activates subsequent signaling pathways, and therefore, regulates the differentiation, function of T, B cells, macrophages, dendritic cells. Recent findings have shown abnormal expression of IL-35 in inflammatory autoimmune diseases, such as systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, multiple sclerosis, type 1 diabetes, psoriasis, multiple sclerosis, autoimmune hepatitis, experimental autoimmune uveitis. In addition, functional analysis suggested that IL-35 is critical in the onset and development of these diseases. Therefore, the present study will systematically review what had been occurred regarding IL-35 in inflammatory autoimmune disease. The information collected will help to understand the biologic role of IL-35 in immune cells, and give information about the therapeutic potential of IL-35 in these diseases.
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