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用于治疗自身免疫性疾病的CCR1拮抗剂。

CCR1 antagonists for the treatment of autoimmune diseases.

作者信息

Gladue Ronald P, Zwillich Samuel H, Clucas Alan T, Brown Matthew F

机构信息

Pfizer Global Research and Development, Department of Immunology, MS 8220-2410, Eastern Point Road, Groton, CT 06340, USA.

出版信息

Curr Opin Investig Drugs. 2004 May;5(5):499-504.

Abstract

Chemokines are 8- to 10-kDa proteins that regulate leukocyte infiltration into inflammatory sites. The therapeutic potential of inhibiting these proteins is supported by their increased expression in human diseases, numerous studies in animal models of disease and, in some cases, by human genetic association studies. These findings, combined with the ability of chemokines to interact with 7-transmembrane G protein-coupled receptors, render them attractive drug discovery targets. This article reviews the evidence that supports a role for the chemokine receptor CCR1 in the pathogenesis of autoimmune diseases, progress made in identifying low molecular-weight antagonists and the current status of agents undergoing clinical evaluation.

摘要

趋化因子是一类分子量为8至10 kDa的蛋白质,可调节白细胞向炎症部位的浸润。人类疾病中趋化因子表达增加、在疾病动物模型中的大量研究以及在某些情况下人类基因关联研究均支持了抑制这些蛋白质的治疗潜力。这些发现,再加上趋化因子与7次跨膜G蛋白偶联受体相互作用的能力,使其成为颇具吸引力的药物研发靶点。本文综述了支持趋化因子受体CCR1在自身免疫性疾病发病机制中起作用的证据、在鉴定低分子量拮抗剂方面取得的进展以及正在进行临床评估的药物的现状。

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