免疫抑制
器官移植
医学
贾纳斯激酶
他克莫司
Janus激酶3
移植
西罗莫司
心脏移植
免疫学
药理学
细胞因子
内科学
T细胞
免疫系统
白细胞介素2受体
作者
Paul S. Changelian,Mark E. Flanagan,Douglas J. Ball,Craig R. Kent,Kelly S. Magnuson,William H. Martin,Bonnie J. Rizzuti,Perry S. Sawyer,Bret D. Perry,William H. Brissette,Sandra P. McCurdy,Elizabeth M. Kudlacz,Maryrose J. Conklyn,Eileen A. Elliott,Erika R. Koslov,Michael B. Fisher,Timothy J. Strelevitz,Kwansik Yoon,David A. Whipple,Jianmin Sun
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2003-10-30
卷期号:302 (5646): 875-878
被引量:662
标识
DOI:10.1126/science.1087061
摘要
Because of its requirement for signaling by multiple cytokines, Janus kinase 3 (JAK3) is an excellent target for clinical immunosuppression. We report the development of a specific, orally active inhibitor of JAK3, CP-690,550, that significantly prolongedsurvival in a murine model of heart transplantation and in cynomolgus monkeys receiving kidney transplants. CP-690,550 treatment was not associatedwith hypertension, hyperlipidemia, or lymphoproliferative disease. On the basis of these preclinical results, we believe JAK3 blockade by CP-690,550 has potential for therapeutically desirable immunosuppression in human organ transplantation andin other clinical settings.
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