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Interactions with Commensal and Pathogenic Bacteria Induce HIV-1 Latency in Macrophages through Altered Transcription Factor Recruitment to the Long Terminal Repeat

Gregory A. Viglianti, Vicente Planelles, Timothy M. Hanley

2021Journal of Virology18 citationsDOIOpen Access PDF

Abstract

The major barrier toward the eradication of HIV-1 infection is the presence of a small reservoir of latently infected cells, which include CD4 + T cells and macrophages that escape immune-mediated clearance and the effects of antiretroviral therapy. There remain crucial gaps in our understanding of the molecular mechanisms that lead to transcriptionally silent or latent HIV-1 infection of macrophages.

Topics & Concepts

BiologyInterferon regulatory factorsTRIFInterferonPsychological repressionTLR4TLR2Viral replicationMicrobiologySignal transducing adaptor proteinVirologyCell biologySignal transductionToll-like receptorInnate immune systemImmunologyImmune systemVirusGeneGeneticsGene expressionHIV Research and TreatmentImmune Cell Function and InteractionReproductive System and Pregnancy
Interactions with Commensal and Pathogenic Bacteria Induce HIV-1 Latency in Macrophages through Altered Transcription Factor Recruitment to the Long Terminal Repeat | Litcius