Volume 36, Issue 3 pp. 706-716
Review Article

HIV latency: experimental systems and molecular models

Shweta Hakre

Shweta Hakre

Gladstone Institute of Virology and Immunology, University of California, San Francisco, CA, USA

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Leonard Chavez

Leonard Chavez

Gladstone Institute of Virology and Immunology, University of California, San Francisco, CA, USA

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Kotaro Shirakawa

Kotaro Shirakawa

Gladstone Institute of Virology and Immunology, University of California, San Francisco, CA, USA

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Eric Verdin

Corresponding Author

Eric Verdin

Gladstone Institute of Virology and Immunology, University of California, San Francisco, CA, USA

Correspondence: Eric Verdin, Gladstone Institute of Virology and Immunology, 1650 Owens St, San Francisco, CA 94941,USA. Tel.: +1 415 734 4808; fax: +1 415 355 0855; e-mail: [email protected]Search for more papers by this author
First published: 28 February 2012
Citations: 2

Abstract

Highly active antiretroviral therapy (HAART) has shown great efficacy in increasing the survival of HIV infected individuals. However, HAART does not lead to the full eradication of infection and therefore has to be continued for life. HIV persists in a transcriptionally inactive form in resting T cells in HAART-treated patients and can be reactivated following T-cell activation. These latently infected cells allow the virus to persist in the presence of HAART. Here, we review recent advances in the study of the molecular mechanisms of HIV latency. We also review experimental models in which latency is currently studied. We focus on the epigenetic mechanisms controlling HIV transcription and on the role of chromatin and its post-translational modifications. We discuss how small molecule inhibitors that target epigenetic regulators, such as HDAC (histone deacetylase) inhibitors, are being tested for their ability to reactivate latent HIV. Finally, we discuss the clinical potential of these drugs to flush out latently infected cells from HIV-infected patients and to eradicate the virus.

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