Ontology highlight
ABSTRACT: Background
One strategy being pursued to clear latently infected cells that persist in people living with HIV (PLWH) on antiretroviral therapy (ART) is to activate latent HIV infection with a latency reversing agent (LRA). Surrogate markers that accurately measure virus production following an LRA are needed.Methods
We quantified cell-associated unspliced (US), multiply spliced (MS) and supernatant (SN) HIV RNA by qPCR from total and resting CD4+ T cells isolated from seven PLWH on ART before and after treatment ex vivo with different LRAs, including histone deacetylase inhibitors (HDACi). MS and plasma HIV RNA were also quantified from PLWH on ART (n-11) who received the HDACi panobinostat.Findings
In total and resting CD4+ T cells from PLWH on ART, detection of US
SUBMITTER: Zerbato JM
PROVIDER: S-EPMC7920823 | biostudies-literature | 2021 Mar
REPOSITORIES: biostudies-literature