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JAK3抑制剂CP-690550在恒河猴长期口服给药后,可选择性降低其血液中NK细胞和CD8+细胞的数量。

The JAK3 inhibitor CP-690550 selectively reduces NK and CD8+ cell numbers in cynomolgus monkey blood following chronic oral dosing.

作者信息

Conklyn Maryrose, Andresen Catharine, Changelian Paul, Kudlacz Elizabeth

机构信息

Pfizer Global Research and Development, Eastern Point Road, Groton, CT 06340, USA.

出版信息

J Leukoc Biol. 2004 Dec;76(6):1248-55. doi: 10.1189/jlb.0504282. Epub 2004 Sep 15.

Abstract

Janus kinase 3 (JAK3) is a cytoplasmic tyrosine kinase associated with the common gamma chain, an integral component of cytokine receptors of the interleukin (IL)-2 family, including IL-4, -7, -9, -15, and -21. CP-690550 is a JAK3 inhibitor with immunosuppressive properties under development for transplantation. We evaluated alterations in circulating lymphocyte subsets in cynomolgus monkey blood following chronic (3-week), oral CP-690550 administration. Natural killer (NK) and CD8+ T cell numbers were reduced in a dose- and time-dependent manner; the latter was a primary effect on memory subsets. CD4+ T and B cell numbers were unaffected or slightly increased, respectively. NK cell numbers were reduced approximately 80% (vs. 35% in vehicle-treated animals) and returned to baseline levels within 3 weeks following treatment cessation. CD8+ T cells declined by a maximum 43% (vs. 25% for vehicle-treated animals) but rebounded significantly (300%) within 2 weeks after the last dose. Although CP-690550 did not result in reduction of CD4+ T cell number, these cells also increased (225%) within 2 weeks of treatment cessation. IL-15 is important for maintaining homeostasis of these cell types, and CP-690550 inhibited IL-15-induced CD69 expression in NK cells [inhibitory concentration 50% (IC50)=48.0+/-8.4 nM] and CD8+ T cells (IC50=16.2+/-1.5 nM).

摘要

Janus激酶3(JAK3)是一种细胞质酪氨酸激酶,与共同γ链相关,共同γ链是白细胞介素(IL)-2家族细胞因子受体的一个组成部分,该家族包括IL-4、-7、-9、-15和-21。CP-690550是一种具有免疫抑制特性的JAK3抑制剂,正在进行移植相关研究。我们评估了食蟹猴长期(3周)口服CP-690550后循环淋巴细胞亚群的变化。自然杀伤(NK)细胞和CD8+T细胞数量呈剂量和时间依赖性减少;后者主要影响记忆亚群。CD4+T细胞和B细胞数量分别未受影响或略有增加。NK细胞数量减少了约80%(与接受赋形剂治疗的动物相比为35%),在停止治疗后3周内恢复到基线水平。CD8+T细胞最多下降43%(与接受赋形剂治疗的动物相比为25%),但在最后一剂后2周内显著反弹(300%)。虽然CP-690550没有导致CD4+T细胞数量减少,但这些细胞在停止治疗后2周内也增加了(225%)。IL-15对维持这些细胞类型的稳态很重要,CP-690550抑制IL-15诱导的NK细胞(半数抑制浓度50%(IC50)=48.0±8.4 nM)和CD8+T细胞(IC50=16.2±1.5 nM)中的CD69表达。

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