Cammack N
Department of Virology, Roche Discovery Welwyn, Welwyn Garden City, UK.
Antivir Chem Chemother. 1999 Mar;10(2):53-62. doi: 10.1177/095632029901000201.
After the identification of CD4 as the primary receptor for human immunodeficiency virus (HIV) type 1 entry into cells of the immune system, it soon became clear that CD4 alone was not sufficient to establish a productive infection. The search for the second receptors or co-receptors started over 10 years ago, and it was not until 1996 that G protein-coupled 7-transmembrane receptors, CXCR4 and CCR5 were finally identified as the co-receptors for HIV-1 entry. The 7-transmembrane receptor family is a familiar therapeutic target for a number of diseases, and therefore these recent findings represent an exciting opportunity for new therapeutic approaches to the treatment of HIV-1 infection.
在确定CD4作为人类免疫缺陷病毒1型(HIV-1)进入免疫系统细胞的主要受体之后,很快就清楚地认识到仅CD4不足以建立有效的感染。对第二种受体或共受体的寻找始于10多年前,直到1996年,G蛋白偶联的7跨膜受体CXCR4和CCR5才最终被确定为HIV-1进入的共受体。7跨膜受体家族是许多疾病常见的治疗靶点,因此这些最新发现为治疗HIV-1感染的新治疗方法带来了令人兴奋的机遇。