Combined approaches for HIV cure
- PMID: 23446138
- PMCID: PMC3966301
- DOI: 10.1097/COH.0b013e32835ef089
Combined approaches for HIV cure
Abstract
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.
Conflict of interest statement
D.J.H. is an employee of Merck Research Laboratories, who hold the license for the clinical HDAC inhibitor, vorinostat.
References
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- Archin NM, Liberty AL, Kashuba AD, et al. Administration of vorinostat disrupts HIV-1 latency in patients on antiretroviral therapy. Nature. 2012;487:482–485. In eight patients, a single dose of 400 mg of the HDAC inhibitor vorinostat induced the upregulation of HIV-RNA expression within resting CD4+ T cells of aviremic HIV-infected patients on ART. - PMC - PubMed
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