Combined approaches for HIV cure

被引:56
作者
Margolis, David M. [1 ]
Hazuda, Daria J. [2 ]
机构
[1] Univ N Carolina, Inst Global Hlth & Infect Dis, Chapel Hill, NC 27599 USA
[2] Merck Res Labs, West Point, PA USA
基金
美国国家卫生研究院;
关键词
HIV; immune response; latency; resting CD4(+) T cells; REACTIVATES LATENT HIV-1; CD4(+) T-CELLS; VALPROIC ACID; INFECTION; ACTIVATION; INHIBITORS; MODEL; INDUCTION; DEPLETION; RESERVOIR;
D O I
10.1097/COH.0b013e32835ef089
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose of review A serious effort has begun to develop therapies that may be capable of eradicating established HIV infection in man. Because of the biological complexity of HIV infection that persists despite potent antiretroviral therapy, it is widely believed that if such therapies can be developed they will involve complex, multimodality approaches. We highlight some of the recent studies in this effort. Recent findings An inhibitor of histone deacetylase has been demonstrated to disrupt latency in man, and new histone deacetylase inhibitors have been identified. Other potential targets, such as histone methyltransferase, protein kinase C, and BRD4, have been recently studied. Model systems, both in primary cells and in animal models, are beginning to be validated. In the clinic, immune-based therapies to aid in the clearance of persistent infection are also being tested. Summary It is too early to know what combination eradication therapies for HIV infection will look like in the future, but candidate therapies and model systems to perform preclinical validation are beginning to take shape.
引用
收藏
页码:230 / 235
页数:6
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