CCR5拮抗剂:对抗艾滋病毒的新工具

Journal of HIV therapy Pub Date : 2005-12-01
Boris Jülg, Frank-Detlef Goebel
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引用次数: 0

摘要

趋化因子受体是HIV进入细胞所必需的。与此过程最相关的两种趋化因子受体是CC趋化因子受体5 (CCR5)和CXC趋化因子受体4 (CXCR4),因为可以通过抑制任一受体来实现疾病的延迟发病。因此,趋化因子受体拮抗剂,特别是CCR5抑制剂,是一类很有前途的新型抗hiv药物。在这篇综述中,我们总结了目前的候选药物,深入了解它们如何与CCR5相互作用,并讨论了这些化合物的要求和限制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CCR5 antagonists: a new tool in fighting HIV.

Chemokine receptors are essential for cell entry by HIV. The two chemokine receptors most relevant to this process are CC chemokine receptor 5 (CCR5) and CXC chemokine receptor 4 (CXCR4) since a delayed onset of disease can be achieved by inhibition of either receptor. Therefore, chemokine receptor antagonists, in particular inhibitors of CCR5, represent a promising new class of anti-HIV agents. In this review, we summarise current drug candidates, give an insight into how they interact with CCR5, and discuss requirements and restrictions for these compounds.

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