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用 Janus 激酶抑制剂 CP-690,550 治疗炎症。

Treating inflammation with the Janus kinase inhibitor CP-690,550.

机构信息

Department of Biology, Daiichi Sankyo Life Science Research Centre in India (RCI), Sector-18, Udyog Vihar Industrial Area, Gurgaon-122 015, Haryana, India.

出版信息

Trends Pharmacol Sci. 2011 Jan;32(1):25-34. doi: 10.1016/j.tips.2010.10.004. Epub 2010 Dec 7.

Abstract

Commonly used immunosuppressants possess several significant dose-limiting toxicities, prompting the search for agents whose mechanisms of action are limited to immune cells. Inhibition of Janus Kinase 3 (JAK3), a hematopoetic cell-restricted tyrosine kinase, represents an attractive target for immunosuppression owing to its limited distribution in tissue and specific role in lymphoid homeostasis. CP-690,550, a JAK3 inhibitor undergoing clinical trials for the treatment of transplant rejection and autoimmune disorders, has shown efficacy similar to comparator immunosuppressants. However, its inhibition of the more ubiquitous JAK family members, JAK1 and JAK2, is a probable cause of drug-related adverse events (e.g. overt immunosuppression, anemia). Here, we argue that CP-690,550 represents only a starting point in the search for a safer small molecule immunosuppressant, and that an isozyme-selective JAK3 inhibitor identified by rational drug design might be substantially safer.

摘要

常用的免疫抑制剂具有几种显著的剂量限制毒性,促使人们寻找作用机制仅限于免疫细胞的药物。Janus 激酶 3(JAK3)的抑制作用,一种造血细胞受限的酪氨酸激酶,由于其在组织中的有限分布和在淋巴组织稳态中的特定作用,代表了免疫抑制的一个有吸引力的靶点。正在进行临床试验以治疗移植排斥和自身免疫性疾病的 JAK3 抑制剂 CP-690,550 已显示出与比较免疫抑制剂相似的疗效。然而,它对更普遍的 JAK 家族成员 JAK1 和 JAK2 的抑制作用可能是药物相关不良事件(例如明显的免疫抑制、贫血)的原因。在这里,我们认为 CP-690,550 只是在寻找更安全的小分子免疫抑制剂的起点,并且通过合理药物设计鉴定的同工酶选择性 JAK3 抑制剂可能会更安全。

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