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靶向趋化因子:病原体能够做到,我们为何不能?

Targeting chemokines: Pathogens can, why can't we?

作者信息

Proudfoot Amanda E I, Bonvin Pauline, Power Christine A

机构信息

Geneva Research Centre, Merck Serono S.A., 9 chemin des Mines, 1202 Genève and NovImmune S.A., 14 chemin des Aulx, 1228 Plan-les-Ouates, Geneva, Switzerland.

Geneva Research Centre, Merck Serono S.A., 9 chemin des Mines, 1202 Genève, Switzerland.

出版信息

Cytokine. 2015 Aug;74(2):259-67. doi: 10.1016/j.cyto.2015.02.011. Epub 2015 Mar 6.

Abstract

Chemoattractant cytokines, or chemokines, are the largest sub-family of cytokines. About 50 distinct chemokines have been identified in humans. Their principal role is to stimulate the directional migration of leukocytes, which they achieve through activation of their receptors, following immobilization on cell surface glycosaminoglycans (GAGs). Chemokine receptors belong to the G protein-coupled 7-transmembrane receptor family, and hence their identification brought great promise to the pharmaceutical industry, since this receptor class is the target for a large percentage of marketed drugs. Unfortunately, the development of potent and efficacious inhibitors of chemokine receptors has not lived up to the early expectations. Several approaches to targeting this system will be described here, which have been instrumental in establishing paradigms in chemokine biology. Whilst drug discovery programs have not yet elucidated how to make successful drugs targeting the chemokine system, it is now known that certain parasites have evolved anti-chemokine strategies in order to remain undetected by their hosts. What can we learn from them?

摘要

趋化因子细胞因子,即趋化因子,是细胞因子中最大的亚家族。在人类中已鉴定出约50种不同的趋化因子。它们的主要作用是刺激白细胞的定向迁移,这是通过它们的受体激活来实现的,受体激活发生在细胞表面糖胺聚糖(GAGs)上固定之后。趋化因子受体属于G蛋白偶联的7跨膜受体家族,因此它们的鉴定给制药行业带来了巨大希望,因为这类受体是大部分已上市药物的靶点。不幸的是,趋化因子受体强效有效抑制剂的开发并未达到早期预期。这里将描述几种针对该系统的方法,这些方法在建立趋化因子生物学范式方面发挥了重要作用。虽然药物研发项目尚未阐明如何成功研发针对趋化因子系统的药物,但现在已知某些寄生虫已经进化出抗趋化因子策略,以便不被宿主发现。我们能从它们身上学到什么呢?

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