CCR5 Antagonism in HIV Infection: Current Concepts and Future Opportunities

被引:50
|
作者
Wilkin, Timothy J. [1 ]
Gulick, Roy M. [1 ]
机构
[1] Cornell Univ, Weill Med Coll, Div Infect Dis, New York, NY 10065 USA
来源
ANNUAL REVIEW OF MEDICINE, VOL 63 | 2012年 / 63卷
关键词
coreceptor tropism; CXCR4; CD4; maraviroc; vicriviroc; TREATMENT-EXPERIENCED PATIENTS; HUMAN-IMMUNODEFICIENCY-VIRUS; THERAPY-NAIVE PATIENTS; SHORT-TERM MONOTHERAPY; ANTIVIRAL ACTIVITY; CLINICAL-TRIALS; R5; HIV-1; ANTIRETROVIRAL THERAPY; MONOCLONAL-ANTIBODY; HAART ERA;
D O I
10.1146/annurev-med-052010-145454
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
CCR5 antagonists inhibit HIV-1 entry by blocking the interaction of HIV-1 with the CCR5 cellular receptor. In patients with established HIV-1 infection, some viral strains use an alternative coreceptor for HIV-1 entry, CXCR4; CCR5 antagonists are not effective in patients harboring these viral strains. Coreceptor tropism testing of viral strains in an individual patient is necessary prior to treating with a CCR5 antagonist. There is one CCR5 antagonist, maraviroc, that is FDA-approved for treatment of HIV-1 infection. This drug is used most commonly for the treatment of HIV-1 infection in patients who have failed other antiretroviral regimens. In addition to virologic effects, CCR5 antagonists are under investigation for immune-modulating effects and for HIV-1 prevention. Ongoing research will further elucidate the role of CCR5 antagonists in combating HIV disease.
引用
收藏
页码:81 / 93
页数:13
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