| Literature DB >> 33717047 |
Alexander O Pasternak1, Christina K Psomas2, Ben Berkhout1.
Abstract
Combination antiretroviral therapy (ART) suppresses human immunodeficiency virus (HIV) replication and improves immune function. However, due to the persistence of long-lived HIV reservoirs, therapy interruption almost inevitably leads to a fast viral rebound. A small percentage of individuals who are able to control HIV replication for extended periods after therapy interruption are of particular interest because they may represent a model of long-term HIV remission without ART. These individuals are characterized by a limited viral reservoir and low reservoir measures can predict post-treatment HIV remission. However, most individuals with a low reservoir still experience fast viral rebound. In this Perspective, we discuss the possible reasons behind this and propose to develop an integral profile, composed of viral and host biomarkers, that could allow the accurate prediction of post-treatment HIV remission. We also propose to incorporate information on the chromatin context of the proviral integration sites into the characterization of the HIV reservoir, as this likely influences the reactivation capacity of latent proviruses and, together with the actual number of intact proviruses, contributes to the replication competence of the reservoir.Entities:
Keywords: HIV; antiretroviral therapy; biomarker; post-treatment controllers; predictive marker; profile; viral reservoir
Year: 2021 PMID: 33717047 PMCID: PMC7952863 DOI: 10.3389/fmicb.2021.648434
Source DB: PubMed Journal: Front Microbiol ISSN: 1664-302X Impact factor: 5.640