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JAK3 inhibition: what potential for the future?

机译:抑制JAK3:未来的潜力是什么?

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摘要

JAK3 inhibition with the CP-690,550 compound has an immunosuppressive potency in murine models, nonhuman primates and humans. This drug blocks STAT5 activation in most T-cell subpopulations but less effectively in T-regulator cells. In low to moderate risk human kidney transplant recipients, combined with mycophenolate mofetil, steroids and an induction with basiliximab, CP-690,550 proved as effective as calcineurin inhibitors with regard to prevention of acute rejection but better than calcineurin inhibitors with regard to preservation of kidney function and histology. However, at the same time, an increased incidence of overimmunosuppression consequences (cytomegalovirus, BK virus and lymphoproliferation) was observed and led to discontinuation of this specific drug development in kidney transplantation.
机译:用CP-690,550化合物抑制JAK3在鼠模型,非人类灵长类动物和人类中具有免疫抑制作用。该药物可在大多数T细胞亚群中阻断STAT5激活,但在T调节细胞中则无效。在中低风险的人类肾脏移植受者中,结合麦考酚酸酯,类固醇和巴利西单抗诱导,CP-690,550在预防急性排斥反应方面被证明与钙调神经磷酸酶抑制剂有效,但在保持肾脏功能方面优于钙调神经磷酸酶抑制剂和组织学。但是,与此同时,观察到过度免疫抑制后果(巨细胞病毒,BK病毒和淋巴增生)的发生率增加,并导致肾脏移植中这种特定药物的开发中断。

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