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JAK-3抑制剂CP-690550在小鼠肺嗜酸性粒细胞增多症模型中是一种有效的抗炎剂。

The JAK-3 inhibitor CP-690550 is a potent anti-inflammatory agent in a murine model of pulmonary eosinophilia.

作者信息

Kudlacz Elizabeth, Conklyn Maryrose, Andresen Catharine, Whitney-Pickett Carrie, Changelian Paul

机构信息

Pfizer Global Research and Development, New London, CT 06320, USA.

出版信息

Eur J Pharmacol. 2008 Mar 17;582(1-3):154-61. doi: 10.1016/j.ejphar.2007.12.024. Epub 2007 Dec 28.

Abstract

Janus kinase 3 (JAK-3) is a tyrosine kinase that has been shown to participate in the signaling of several cytokines that are believed to play a role in allergic airway disease, e.g. IL-2, 4 and 9. The current study describes the immunosuppressive effects of CP-690550, a novel, small molecule inhibitor of JAK-3, in a murine model of allergic pulmonary inflammation. In vitro, CP-690550 potently inhibited IL-4 induced upregulation of CD23 (IC(50)=57 nM) and class II major histocompatibility complex (MHCII) expression (IC(50)=71 nM) on murine B cells. Repeat aerosol exposure to ovalbumin in wild-type mice sensitized to the antigen resulted in preferential recruitment of Th2-like cells (IL-4+ and IL-5+) into bronchoalveolar lavage fluid (BAL). The importance of IL-4 in the development of pulmonary eosinophilia was supported by a marked (90%) reduction in the influx of these cells in IL-4KO mice similarly sensitized and ovalbumin exposed. Animals dosed with CP-690550 (15 mg/kg/d) during the period of antigen sensitization and boost demonstrated marked reductions in BAL eosinophils and levels of IL-13 and eotaxin following ovalbumin aerosol exposure. The JAK-3 inhibitor (1.5-15 mg/kg/d) also effectively reduced the same parameters when administered during the period of antigen challenge. In contrast, the calcineurin inhibitor tacrolimus (10 mg/kg) was effective only when administered during the period of ovalbumin aerosol exposure. These data support the participation of JAK-3 in processes that contribute to pulmonary eosinophilia in the allergic mouse model. CP-690550 represents an intriguing novel therapy for treatment of allergic conditions associated with airway eosinophilia including asthma and rhinitis.

摘要

Janus激酶3(JAK-3)是一种酪氨酸激酶,已被证明参与多种细胞因子的信号传导,这些细胞因子被认为在过敏性气道疾病中起作用,例如白细胞介素-2、4和9。本研究描述了新型小分子JAK-3抑制剂CP-690550在过敏性肺部炎症小鼠模型中的免疫抑制作用。在体外,CP-690550能有效抑制白细胞介素-4诱导的小鼠B细胞上CD23上调(半数抑制浓度[IC50]=57 nM)和II类主要组织相容性复合体(MHCII)表达(IC50=71 nM)。对致敏于该抗原的野生型小鼠重复雾化暴露卵清蛋白,导致类似Th2的细胞(白细胞介素-4+和白细胞介素-5+)优先募集到支气管肺泡灌洗液(BAL)中。在同样致敏并暴露于卵清蛋白的白细胞介素-4基因敲除小鼠中,这些细胞的流入量显著减少(90%),这支持了白细胞介素-4在肺部嗜酸性粒细胞增多症发展中的重要性。在抗原致敏和激发期间给予CP-690550(15毫克/千克/天)的动物,在暴露于卵清蛋白雾化后,BAL中的嗜酸性粒细胞以及白细胞介素-13和嗜酸性粒细胞趋化因子水平显著降低。当在抗原激发期间给药时,JAK-3抑制剂(1.5 - 15毫克/千克/天)也能有效降低相同参数。相比之下,钙调神经磷酸酶抑制剂他克莫司(10毫克/千克)仅在卵清蛋白雾化暴露期间给药才有效。这些数据支持JAK-3参与了过敏性小鼠模型中导致肺部嗜酸性粒细胞增多的过程。CP-690550代表了一种用于治疗与气道嗜酸性粒细胞增多相关的过敏性疾病(包括哮喘和鼻炎)的有趣新疗法。

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