Activation of Latent HIV-1 T Cell Reservoirs with a Combination of Innate Immune and Epigenetic Regulators

Author:

Palermo Enrico1,Acchioni Chiara2,Di Carlo Daniele3,Zevini Alessandra1,Muscolini Michela1,Ferrari Matteo1,Castiello Luciano1,Virtuoso Sara4,Borsetti Alessandra4,Antonelli Guido3,Turriziani Ombretta3,Sgarbanti Marco2ORCID,Hiscott John1

Affiliation:

1. Pasteur Institute—Italy, Istituto Pasteur—Fondazione Cenci Bolognetti, Rome, Italy

2. Department of Infectious, Parasitic and Immune-Mediated Diseases, Istituto Superiore di Sanità, Rome, Italy

3. Department of Molecular Medicine, Sapienza University of Rome, Rome, Italy

4. National HIV/AIDS Research Center, Istituto Superiore di Sanità, Rome, Italy

Abstract

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.

Funder

HHS | National Institutes of Health

Associazione Italiana per la Ricerca sul Cancro

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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