Carter Percy H
Bristol-Myers Squibb Company, Experimental Station, Wilmington, DE 19880-0500, USA.
Curr Opin Chem Biol. 2002 Aug;6(4):510-25. doi: 10.1016/s1367-5931(02)00351-4.
Inflammation plays a pivotal role in exacerbating a wide array of human diseases. The chemokines are a group of proteins that control the movement and activation of the immune cells involved in all aspects of the inflammatory response. Recently, their cognate receptors have attracted considerable interest as therapeutic targets, in part because they are G-protein-coupled receptors, which have been antagonized successfully before by the pharmaceutical industry. Indeed, several companies have now reported the development of selective small-molecule chemokine receptor antagonists, and some of these compounds have even entered human Phase I clinical trials. Preclinical studies of the responsiveness of murine models of inflammation to either pharmacologic or genetic intervention have suggested that antagonism of some chemokine receptors may well prove to be a safe and efficacious approach to anti-inflammatory therapy.
炎症在加剧多种人类疾病方面起着关键作用。趋化因子是一类蛋白质,可控制参与炎症反应各个方面的免疫细胞的移动和激活。最近,它们的同源受体作为治疗靶点引起了相当大的关注,部分原因是它们是G蛋白偶联受体,制药行业此前已成功研制出针对这类受体的拮抗剂。事实上,现在已有几家公司报告了选择性小分子趋化因子受体拮抗剂的研发情况,其中一些化合物甚至已进入人体I期临床试验。对炎症小鼠模型对药物或基因干预反应性的临床前研究表明,拮抗某些趋化因子受体很可能被证明是一种安全有效的抗炎治疗方法。