Entry inhibitors in the treatment of HIV-1 infection

被引:161
|
作者
Tilton, John C. [1 ]
Doms, Robert W. [1 ]
机构
[1] Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA
关键词
HIV; Entry inhibitors; Maraviroc; Enfuvirtide; Highly active antiretroviral therapy (HAART); HUMAN-IMMUNODEFICIENCY-VIRUS; SYNCYTIUM-INDUCING PHENOTYPE; CHEMOKINE RECEPTOR CXCR4; ENFUVIRTIDE RESISTANCE MUTATIONS; TREATMENT EXPERIENCED PATIENTS; ENVELOPE GLYCOPROTEIN TRIMERS; CCR5; MONOCLONAL-ANTIBODY; SMALL-MOLECULE; ANTIVIRAL ACTIVITY; V3; LOOP;
D O I
10.1016/j.antiviral.2009.07.022
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Infection of target cells by HIV is a complex, multi-stage process involving attachment to host cells and CD4 binding, coreceptor binding, and membrane fusion. Drugs that block HIV entry are collectively known as entry inhibitors, but comprise a complex group of drugs with multiple mechanisms of action depending on the stage of the entry process at which they act. Two entry inhibitors, maraviroc and enfuvirtide, have been approved for the treatment of HIV-1 infection, and a number of agents are in development. This review covers the entry inhibitors and their use in the management of HIV-1 infection. This article forms part of a special issue of Antiviral Research marking the 25th anniversary of antiretroviral drug discovery and development, Vol 85, issue 1, 2010. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:91 / 100
页数:10
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