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调节趋化因子网络的新型疗法。

New therapeutics that modulate chemokine networks.

作者信息

Schwarz Matthias K, Wells Timothy N C

机构信息

Serono Pharmaceutical Research Institute, 14 Chemin des Aulx, 1228 Plan-les-Ouates, Geneva, Switzerland.

出版信息

Nat Rev Drug Discov. 2002 May;1(5):347-58. doi: 10.1038/nrd795.

Abstract

Chemokines are small cytokines that control a wide variety of biological and pathological processes, from immunosurveillance to inflammation, and from viral infection to cancer. The numerous known chemokine receptors have given hope that selective receptor antagonism might be possible, which could allow us to control which cells are recruited and activated at any time and in any place. As chemokine receptors are G-protein-coupled receptors, which are classical targets for the pharmaceutical industry, it is hoped that chemokines could be the first cytokines for which small-molecule receptor antagonists could be developed. Recently, reports of chemokine-receptor antagonists, both in vitro and in animal models of disease, have been published. It is anticipated that this field could produce clinically useful therapies in the next few years.

摘要

趋化因子是一类小细胞因子,可控制从免疫监视到炎症、从病毒感染到癌症等各种各样的生物学和病理学过程。众多已知的趋化因子受体让人们看到了实现选择性受体拮抗作用的希望,这可能使我们能够随时、随地控制哪些细胞被募集和激活。由于趋化因子受体是G蛋白偶联受体,而这类受体是制药行业的经典靶点,因此人们希望趋化因子能够成为首批可开发小分子受体拮抗剂的细胞因子。最近,已有关于趋化因子受体拮抗剂在体外和疾病动物模型中的报道发表。预计在未来几年内,该领域可能会产生具有临床应用价值的治疗方法。

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