HIV-1 cell entry and advances in viral entry inhibitor therapy

被引:52
|
作者
Cooley, LA
Lewin, SR [1 ]
机构
[1] Royal Melbourne Hosp, Victorian Infect Dis Serv, Parkville, Vic 3050, Australia
[2] Royal Melbourne Hosp, Victorian Infect Dis Reference Lab, Parkville, Vic 3050, Australia
[3] Univ Melbourne, Dept Microbiol & Immunol, Parkville, Vic 3052, Australia
关键词
HIV-1 cell entry; HIV-1 entry inhibitor; HIV-1 fusion inhibitor; antiretroviral therapy;
D O I
10.1016/S1386-6532(02)00111-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Despite the considerable successes of highly active antiretroviral therapy, new classes of therapeutic agents are still urgently needed. Unfortunately, the emergence of antiviral resistance and drug toxicity remain challenging obstacles to successful treatment in many HIV-1-infected individuals. HIV-1 entry is a multi-step process that is an attractive target for the development of new classes of therapeutic agents. Considerable progress has been made in the understanding of HIV-1 cell entry, enabling the design of specific agents that can inhibit each step of cellular entry. A number of promising agents have commenced clinical trials, including the attachment inhibitor PRO 542, co-receptor inhibitor AMD3100 and fusion inhibitor T-20. A greater number of HIV-1 entry inhibitors are in preclinical development. This review outlines the mechanisms involved in HIV-1 entry and the sites,of action of specific HIV-1 inhibitors. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:121 / 132
页数:12
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