JAK3抑制:未来的潜力是什么?

Christophe Legendre
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引用次数: 3

摘要

用CP-690,550化合物抑制JAK3在小鼠模型、非人灵长类动物和人类中具有免疫抑制效力。这种药物在大多数t细胞亚群中阻断STAT5的激活,但在t调节细胞中效果较差。在低至中等风险的人肾移植受者中,联合麦考酚酸酯、类固醇和巴氏昔单抗诱导,CP-690,550在预防急性排斥反应方面与钙调磷酸酶抑制剂一样有效,但在保存肾功能和组织学方面优于钙调磷酸酶抑制剂。然而,与此同时,观察到过度免疫抑制后果(巨细胞病毒、BK病毒和淋巴细胞增殖)的发生率增加,并导致肾移植中这种特异性药物的开发停止。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

JAK3 inhibition: what potential for the future?

JAK3 inhibition: what potential for the future?

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.

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