Publication | Open Access
Activation of Latent HIV-1 T Cell Reservoirs with a Combination of Innate Immune and Epigenetic Regulators
25
Citations
47
References
2019
Year
Hiv-1 LoadsT-regulatory CellImmune RegulationImmunologyInnate ImmunityAntiviral DrugImmune SystemImmunotherapyHiv EradicationHuman RetrovirusAutoimmunityT Cell ImmunityChronic Viral InfectionHivCell BiologyAids PathogenesisAntiviral ResponseAntiviral TherapyInnate ImmuneDi-cyclic Nucleotide CgampEpigenetic RegulatorsMedicineViral Immunity
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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