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Activation of Latent HIV-1 T Cell Reservoirs with a Combination of Innate Immune and Epigenetic Regulators
Author(s) -
Enrico Palermo,
Chiara Acchioni,
Daniele Di Carlo,
Alessandra Zevini,
Michela Muscolini,
Matteo Ferrari,
Luciano Castiello,
Sara Virtuoso,
Alessândra Borsetti,
Guido Antonelli,
Ombretta Turriziani,
Marco Sgarbanti,
John Hiscott
Publication year - 2019
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.01194-19
Subject(s) - biology , innate immune system , epigenetics , human immunodeficiency virus (hiv) , immune system , microbiology and biotechnology , innate lymphoid cell , virology , immunology , computational biology , genetics , gene
One of the challenges associated with HIV-1 infection is that despite antiretroviral therapies that reduce HIV-1 loads to undetectable levels, proviral DNA remains dormant in a subpopulation of T lymphocytes. Numerous strategies to clear residual virus by reactivating latent virus and eliminating the reservoir of HIV-1 (so-called “shock-and-kill” strategies) have been proposed. In the present study, we use a combination of small molecules that activate the cGAS-STING antiviral innate immune response (the di-cyclic nucleotide cGAMP) and epigenetic modulators (histone deacetylase inhibitors) that induce reactivation and HIV-infected T cell killing in cell lines, primary T lymphocytes, and patient samples. These studies represent a novel strategy for HIV eradication by reducing the viral reservoir and inducing specific death of HIV-infected cells.

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