Prevention of organ allograft rejection by a specific Janus kinase 3 inhibitor

被引:548
作者
Changelian, PS [1 ]
Flanagan, ME
Ball, DJ
Kent, CR
Magnuson, KS
Martin, WH
Rizzuti, BJ
Sawyer, PS
Perry, BD
Brissette, WH
McCurdy, SP
Kudlacz, EM
Conklyn, MJ
Elliott, EA
Koslov, ER
Fisher, MB
Strelevitz, TJ
Yoon, K
Whipple, DA
Sun, JM
Munchhof, MJ
Doty, JL
Casavant, JM
Blumenkopf, TA
Hines, M
Brown, MF
Lillie, BM
Subramanyam, C
Shang-Poa, C
Milici, AJ
Beckius, GE
Moyer, JD
Su, CY
Woodworth, TG
Gaweco, AS
Beals, CR
Littman, BH
Fisher, DA
Smith, JF
Zagouras, P
Magna, HA
Saltarelli, MJ
Johnson, KS
Nelms, LF
Des Etages, SG
Hayes, LS
Kawabata, TT
Finco-Kent, D
Baker, DL
Larson, M
机构
[1] Pfizer Global Res & Dev, Dept Antibacterials & Immunol, Immunol Grp, Groton, CT 06340 USA
[2] Pfizer Global Res & Dev, Dept Drug Safety Evaluat, Groton, CT 06340 USA
[3] Pfizer Global Res & Dev, Dept Pharmacokinet Dynam & Metab, Groton, CT 06340 USA
[4] Pfizer Global Res & Dev, Dept Genom & Proteom Sci, Groton, CT 06340 USA
[5] Stanford Univ, Sch Med, Transplantat Immunol Lab, Stanford, CA 94305 USA
[6] NIH, Mol Immunol & Inflammat Branch, Bethesda, MD 20892 USA
关键词
D O I
10.1126/science.1087061
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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 prolonged survival in a murine model of heart transplantation and in cynomolgus monkeys receiving kidney transplants. CP-690,550 treatment was not associated with 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 and in other clinical settings.
引用
收藏
页码:875 / 878
页数:4
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