Therapeutic targeting of human immunodeficiency virus type-1 latency: current clinical realities and future scientific possibilities

被引:27
作者
Butera, ST [1 ]
机构
[1] Ctr Dis Control & Prevent, HIV & Retrovirol Branch, Div AIDS STD, Atlanta, GA 30333 USA
[2] Ctr Dis Control & Prevent, Natl Ctr Infect Dis, TB Lab Res, Atlanta, GA 30333 USA
关键词
HIV-1; latency; therapeutic intervention; cell models; viral transcription;
D O I
10.1016/S0166-3542(00)00133-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Factors affecting HIV-1 latency present formidable obstacles for therapeutic intervention. As these obstacles have become a clinical reality, even with the use of potent anti-retroviral regimens, the need for novel therapeutic strategies specifically targeting HIV-1 latency is evident. However, therapeutic targeting of HIV-1 latency requires an understanding of the mechanisms regulating viral quiescence and activation. These mechanisms have been partially delineated using chronically infected cell models and, dearly, HIV-I activation from latency involves several key viral and cellular components. Among these distinctive therapeutic targets, cellular factors involved in HIV-1 transcription especially warrant further consideration for rational drug design. Exploring the scientific possibilities of new therapies targeting HIV-1 latency may hold new promise of eventual HIV-1 eradication. (C) 2000 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:143 / 176
页数:34
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