| Literature DB >> 30198905 |
Abraham J Kandathil1, Sho Sugawara1, Ashish Goyal2, Christine M Durand1, Jeffrey Quinn1, Jaiprasath Sachithanandham1, Andrew M Cameron3, Justin R Bailey1, Alan S Perelson2, Ashwin Balagopal1.
Abstract
Long-lived HIV-1 reservoirs that persist despite antiretroviral therapy (ART) are a major impediment to a cure for HIV-1. We examined whether human liver macrophages (LMs), the largest tissue macrophage population, comprise an HIV-1 reservoir. We purified LMs from liver explants and included treatment with a T cell immunotoxin to reduce T cells to 1% or less. LMs were purified from 9 HIV-1-infected persons, 8 of whom were on ART (range 8-140 months). Purified LMs were stimulated ex vivo and supernatants from 6 of 8 LMs from persons on ART transmitted infection. However, HIV-1 propagation from LMs was not sustained except in LMs from 1 person taking ART for less than 1 year. Bulk liver sequences matched LM-derived HIV-1 in 5 individuals. Additional in vitro experiments undertaken to quantify the decay of HIV-1-infected LMs from 3 healthy controls showed evidence of infection and viral release for prolonged durations (>170 days). Released HIV-1 propagated robustly in target cells, demonstrating that viral outgrowth was observable using our methods. The t1/2 of HIV-1-infected LMs ranged from 3.8-55 days. These findings suggest that while HIV-1 persists in LMs during ART, it does so in forms that are inert, suggesting that they are defective or restricted with regard to propagation.Entities:
Keywords: AIDS/HIV; Infectious disease; Macrophages
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Year: 2018 PMID: 30198905 PMCID: PMC6159970 DOI: 10.1172/JCI121678
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808