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No recovery of replication-competent HIV-1 from human liver macrophages.
Kandathil, Abraham J; Sugawara, Sho; Goyal, Ashish; Durand, Christine M; Quinn, Jeffrey; Sachithanandham, Jaiprasath; Cameron, Andrew M; Bailey, Justin R; Perelson, Alan S; Balagopal, Ashwin.
Affiliation
  • Kandathil AJ; Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
  • Sugawara S; Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
  • Goyal A; Theoretical Biology and Biophysics, Los Alamos National Laboratory, Los Alamos, New Mexico, USA.
  • Durand CM; Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
  • Quinn J; Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
  • Sachithanandham J; Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
  • Cameron AM; Department of Surgery, Johns Hopkins University, Baltimore, Maryland, USA.
  • Bailey JR; Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
  • Perelson AS; Theoretical Biology and Biophysics, Los Alamos National Laboratory, Los Alamos, New Mexico, USA.
  • Balagopal A; Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
J Clin Invest ; 128(10): 4501-4509, 2018 10 01.
Article in En | MEDLINE | ID: mdl-30198905
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Virus Replication / HIV Infections / HIV-1 / Liver / Macrophages Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: J Clin Invest Year: 2018 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Virus Replication / HIV Infections / HIV-1 / Liver / Macrophages Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: J Clin Invest Year: 2018 Document type: Article Affiliation country: United States Country of publication: United States