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Widespread distribution of transcriptionally active, clonally expanded, HIV-1 proviruses despite suppressive antiretroviral therapy

  1. Author:
    Imamichi, Hiromi
    Natarajan,Venkatachala
    Scrimieri,Francesca
    Smith, Mindy
    Badralmaa,Yunden
    Bosche,Marjorie
    Hensien, Jack M
    Buerkert, Thomas
    Sherman,Brad
    Sherman, Brad T
    Singh, Kanal
    Lane, H Clifford
  2. Author Address

    Clinical and Molecular Retrovirology Section, NIH, Bethesda, United States of America., Clinical Services Program, Frederick National Laboratory for Cancer Research, Frederick, United States of America.,
    1. Year: 2025
    2. Date: Apr 22
    3. Epub Date: 2025 04 22
  1. Journal: The Journal of Clinical Investigation
  2. Type of Article: Article
  3. Article Number: e190824
  1. Abstract:

    The rapid viral rebound observed following treatment interruption, despite prolonged time on antiretroviral therapy with plasma HIV-RNA levels <40 copies/mL, suggests persistent HIV-1 reservoir(s) outside of the blood. Studies of HIV-1 proviruses in autopsy tissue samples have hinted at their persistence. However, their distribution across different anatomical compartments and their transcriptional activity within tissues remains unclear. The present study has examined molecular DNA and RNA reservoirs of HIV-1 in autopsy samples from 13 individuals with HIV-1 infection. Of the 13, 5 had detectable levels of HIV-1 RNA in plasma while 8 did not. Cell associated HIV-RNA was detected in 12 out of 13 donors and in 27 of the 30 different tissues examined. HIV-specific DNA and RNA were widely distributed and predominantly associated with clonal expansions. No significant differences were noted between the groups and no tissues were preferentially affected. These data imply that a substantial seeding of tissues with cells harboring transcriptionally active proviral DNA can be seen in the setting of HIV-1 infection despite ART and highlight one of the challenges in achieving an HIV-1 cure.

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External Sources

  1. DOI: 10.1172/JCI190824
  2. PMID: 40299750
  3. PII : 190824

Library Notes

  1. Fiscal Year: FY2024-2025
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