免疫学
免疫系统
医学
自身免疫性疾病
自身免疫
类风湿性关节炎
发病机制
疾病
抗体
病理
作者
Min Zhang,Linglong Peng,Ying Wang,Jian‐Shu Wang,Jiao Liu,Mengmeng Liu,Jia Hu,Bin Song,Haibing Yang
出处
期刊:Immunologic Research
[Springer Science+Business Media]
日期:2015-07-01
卷期号:64 (2): 337-344
被引量:50
标识
DOI:10.1007/s12026-015-8677-6
摘要
A20 (TNFAIP3), known to inhibit NF-κB function by deubiquitinating-specific NF-κB signaling molecules, has been found in many cell types of the immune system. Recent findings suggest that A20 is essential for the development and functional performance of dendritic cell, B cell, T cell and macrophage. A number of studies further demonstrate that these cells are crucial in the pathogenesis of autoimmune diseases, such as type 1 diabetes, systemic lupus erythematosus, inflammatory bowel disease, ankylosing arthritis, Sjogren's syndrome and rheumatoid arthritis. In this article, we focus on the recent advances on the roles of A20 in autoimmune diseases and discuss the therapeutic significance of these new findings.
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