Chemokine receptor antagonism as an approach to anti-inflammatory therapy: 'just right' or plain wrong?

被引:52
|
作者
Carter, PH [1 ]
机构
[1] Bristol Myers Squibb Co, Expt Stn, Wilmington, DE 19880 USA
关键词
D O I
10.1016/S1367-5931(02)00351-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:510 / 525
页数:16
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