激酶
贾纳斯激酶
免疫系统
酪氨酸激酶
受体酪氨酸激酶
生物
癌症研究
信号转导
布鲁顿酪氨酸激酶
免疫学
细胞生物学
作者
Leslie Castelo‐Soccio,Hanna Kim,Massimo Gadina,Pamela L. Schwartzberg,Arian Laurence,John J. O’Shea
出处
期刊:Nature Reviews Immunology
[Springer Nature]
日期:2023-05-15
卷期号:23 (12): 787-806
被引量:41
标识
DOI:10.1038/s41577-023-00877-7
摘要
Protein kinases play a major role in cellular activation processes, including signal transduction by diverse immunoreceptors. Given their roles in cell growth and death and in the production of inflammatory mediators, targeting kinases has proven to be an effective treatment strategy, initially as anticancer therapies, but shortly thereafter in immune-mediated diseases. Herein, we provide an overview of the status of small molecule inhibitors specifically generated to target protein kinases relevant to immune cell function, with an emphasis on those approved for the treatment of immune-mediated diseases. The development of inhibitors of Janus kinases that target cytokine receptor signalling has been a particularly active area, with Janus kinase inhibitors being approved for the treatment of multiple autoimmune and allergic diseases as well as COVID-19. In addition, TEC family kinase inhibitors (including Bruton's tyrosine kinase inhibitors) targeting antigen receptor signalling have been approved for haematological malignancies and graft versus host disease. This experience provides multiple important lessons regarding the importance (or not) of selectivity and the limits to which genetic information informs efficacy and safety. Many new agents are being generated, along with new approaches for targeting kinases.
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