| Literature DB >> 32300019 |
Viviane M Andrade1, Carla Mavian2, Dunja Babic3, Thaissa Cordeiro3, Mark Sharkey3, Labelle Barrios3, Christian Brander4, Javier Martinez-Picado4, Judith Dalmau4, Anuska Llano4, Jonathan Z Li5, Jeffrey Jacobson6, Christy L Lavine7, Michael S Seaman7, Marco Salemi2, Mario Stevenson8,9.
Abstract
HIV-1 persists in cellular reservoirs that can reignite viremia if antiretroviral therapy (ART) is interrupted. Therefore, insight into the nature of those reservoirs may be revealed from the composition of recrudescing viremia following treatment cessation. A minor population of macrophage-tropic (M-tropic) viruses was identified in a library of recombinant viruses constructed with individual envelope genes that were obtained from plasma of six individuals undergoing analytic treatment interruption (ATI). M-tropic viruses could also be enriched from post-ATI plasma using macrophage-specific (CD14) but not CD4+ T cell-specific (CD3) antibodies, suggesting that M-tropic viruses had a macrophage origin. Molecular clock analysis indicated that the establishment of M-tropic HIV-1 variants predated ATI. Collectively, these data suggest that macrophages are a viral reservoir in HIV-1-infected individuals on effective ART and that M-tropic variants can appear in rebounding viremia when treatment is interrupted. These findings have implications for the design of curative strategies for HIV-1.Entities:
Keywords: HIV-1 reservoirs; analytical treatment interruption; macrophages
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Year: 2020 PMID: 32300019 PMCID: PMC7211992 DOI: 10.1073/pnas.1917034117
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205