酪氨酸激酶2
免疫学
银屑病
信号转导
医学
免疫系统
自身免疫性疾病
JAK-STAT信号通路
自身免疫
发病机制
酪氨酸激酶
炎症
贾纳斯激酶
细胞因子
癌症研究
生物
受体
细胞生物学
抗体
生长因子
血小板源性生长因子受体
内科学
作者
Maciej Gonciarz,Katarzyna Pawlak‐Buś,Piotr Leszczyński,Witold Owczarek
出处
期刊:Immunotherapy
[Future Medicine]
日期:2021-07-08
卷期号:13 (13): 1135-1150
被引量:36
标识
DOI:10.2217/imt-2021-0096
摘要
JAKs are intracellular protein tyrosine kinases that, through activation of STATs, are responsible for signal transduction pathways that regulate cellular responses to numerous cytokines, growth factors and hormones in many different cells. JAK-STAT signaling plays a key role in regulating immune function, and cytokines - such as IL-23, IL-12 and type I interferons - are central to the pathogenesis of autoimmune diseases, including psoriasis, inflammatory bowel disease and systemic lupus erythematosus. Here the authors review the evidence for targeting TYK2 as a more specific approach to treating these conditions. TYK2 inhibitors are clinically effective in autoimmune and inflammatory diseases and may avoid some of the complications reported with nonselective JAK inhibitors.
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