Chemokine receptors and their interactors in HIV-1 replication: potential therapeutic targets

Chuan Li, Yi-jie Zhang, D. Dupré, Yi‐Qun Kuang
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Abstract

Chemokine receptors CXCR4 and CCR5 are co-receptors indispensable for human immunodeficiency virus type 1 (HIV-1) entry and subsequent infection in host cells. Antiretroviral therapies based on the viral proteins have been developed, and significant achievements have been made in the treatment of HIV/AIDS patients based on the HAART regimens. However, a lot of concerns are still present, the purge of latent viral reservoirs and cure of AIDS are currently impossible, and prophylactic vaccines are not yet available. Most recently, HIV-1 entry has been understood much more and targeting viral entry based on chemokine receptors represents an interesting prospective. In this research highlight, we review the role of HIV-1 co-receptors-interacting proteins during chemokine receptor signal activation and assembly, as well as present new results about how they can regulate the replication of the virus.
趋化因子受体及其在HIV-1复制中的相互作用:潜在的治疗靶点
趋化因子受体CXCR4和CCR5是人类免疫缺陷病毒1型(HIV-1)进入宿主细胞和随后感染必不可少的共受体。基于病毒蛋白的抗逆转录病毒疗法已经开发出来,并且在基于HAART方案治疗艾滋病毒/艾滋病患者方面取得了重大成就。然而,许多问题仍然存在,清除潜伏病毒库和治愈艾滋病目前是不可能的,预防性疫苗尚未问世。最近,人们对HIV-1的进入有了更多的了解,基于趋化因子受体靶向病毒进入代表了一个有趣的前景。在本研究重点中,我们回顾了HIV-1共受体相互作用蛋白在趋化因子受体信号激活和组装过程中的作用,并介绍了它们如何调节病毒复制的新结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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