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激酶抑制在自身免疫和炎症中的作用。

Kinase inhibition in autoimmunity and inflammation.

机构信息

Discovery Department, TRex Bio, South San Francisco, CA, USA.

Early Discovery Biochemistry Department, Genentech, South San Francisco, CA, USA.

出版信息

Nat Rev Drug Discov. 2021 Jan;20(1):39-63. doi: 10.1038/s41573-020-0082-8. Epub 2020 Oct 19.

Abstract

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.

摘要

尽管在治疗自身免疫和炎症性疾病方面取得了一些进展,但在某些领域仍存在尚未满足的医疗需求。减轻失调性炎症的主要治疗方法之一是针对调节炎症介质产生的激酶的活性。小分子激酶抑制剂具有广泛疗效、方便性和组织穿透性的潜力,因此通常比生物制剂具有重要优势。然而,设计具有靶向选择性和最小脱靶效应的激酶抑制剂可能具有挑战性。尽管如此,在将具有理想药物特性的激酶抑制剂推进临床应用方面已经取得了巨大进展,包括 JAK、IRAK4、RIPK、BTK、SYK 和 TPL2 的抑制剂。本综述将重点介绍临床验证的自身免疫和炎症途径,介绍激酶抑制剂的最新发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/273e/7569567/02afa2518f6b/41573_2020_82_Fig1_HTML.jpg

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