Block-And-Lock Strategies to Cure HIV Infection

被引:124
作者
Vansant, Gerlinde [1 ]
Bruggemans, Anne [1 ]
Janssens, Julie [1 ]
Debyser, Zeger [1 ]
机构
[1] Katholieke Univ Leuven, Dept Pharmaceut & Pharmacol Sci, Lab Mol Virol & Gene Therapy, B-3000 Leuven, Flanders, Belgium
来源
VIRUSES-BASEL | 2020年 / 12卷 / 01期
关键词
HIV; latency; cure; block-and-lock; RNA-POLYMERASE-II; STEM-CELL TRANSPLANTATION; SMALL-MOLECULE INHIBITORS; LONG TERMINAL REPEAT; P-TEFB; T-CELLS; DEACETYLASE INHIBITORS; DIDEHYDRO-CORTISTATIN; TRANSCRIPTION; REPLICATION;
D O I
10.3390/v12010084
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Today HIV infection cannot be cured due to the presence of a reservoir of latently infected cells inducing a viral rebound upon treatment interruption. Hence, the latent reservoir is considered as the major barrier for an HIV cure. So far, efforts to completely eradicate the reservoir via a shock-and-kill approach have proven difficult and unsuccessful. Therefore, more research has been done recently on an alternative block-and-lock functional cure strategy. In contrast to the shock-and-kill strategy that aims to eradicate the entire reservoir, block-and-lock aims to permanently silence all proviruses, even after treatment interruption. HIV silencing can be achieved by targeting different factors of the transcription machinery. In this review, we first describe the underlying mechanisms of HIV transcription and silencing. Next, we give an overview of the different block-and-lock strategies under investigation.
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页数:17
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