自身免疫
激酶
锡克
布鲁顿酪氨酸激酶
医学
贾纳斯激酶
炎症
酪氨酸激酶
药物发现
免疫学
生物信息学
生物
细胞因子
免疫系统
受体
细胞生物学
内科学
作者
Ali A. Zarrin,Katherine Bao,Patrick J. Lupardus,Domagoj Vucic
标识
DOI:10.1038/s41573-020-0082-8
摘要
Despite recent advances in the treatment of autoimmune and inflammatory diseases, unmet medical needs in some areas still exist. One of the main therapeutic approaches to alleviate dysregulated inflammation has been to target the activity of kinases that regulate production of inflammatory mediators. Small-molecule kinase inhibitors have the potential for broad efficacy, convenience and tissue penetrance, and thus often offer important advantages over biologics. However, designing kinase inhibitors with target selectivity and minimal off-target effects can be challenging. Nevertheless, immense progress has been made in advancing kinase inhibitors with desirable drug-like properties into the clinic, including inhibitors of JAKs, IRAK4, RIPKs, BTK, SYK and TPL2. This Review will address the latest discoveries around kinase inhibitors with an emphasis on clinically validated autoimmunity and inflammatory pathways.
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