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No evidence of HIV replication in children on antiretroviral therapy

  1. Author:
    Van Zyl, Gert U
    Katusiime, Mary Grace
    Wiegand, Ann
    McManus, William
    Bale, Michael
    Halvas, Elias K
    Luke, Brian
    Boltz, Valerie
    Spindler, Jon
    Laughton, Barbara
    Engelbrecht, Susan
    Coffin, John M
    Cotton, Mark F
    Shao, Wei
    Mellors, John W
    Kearney, Mary
  2. Author Address

    Division of Medical Virology, Stellenbosch University and National Health Laboratory Service (NHLS) Tygerberg, Cape Town, South Africa., HIV Dynamics and Replication Program, National Cancer Institute (NCI), Frederick, Maryland, USA., Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA., Advanced Biomedical Computing Center, Leidos Biomedical Research Inc. and Frederick National Laboratories for Cancer Research, Frederick, Maryland, USA., Department Pediatrics and Child Health, Tygerberg Children 39;s Hospital and Family Clinical Research Unit, Stellenbosch University, Cape Town, South Africa., Department of Molecular Biology and Microbiology, Tufts University, Boston Massachusetts, USA.,
    1. Year: 2017
    2. Date: Oct 2
    3. Epub Date: 2017 Sep 11
  1. Journal: Journal of Clinical Investigation
    1. 127
    2. 10
    3. Pages: 3827-3834
  2. Type of Article: Article
  3. ISSN: 0021-9738
  1. Abstract:

    It remains controversial whether current antiretroviral therapy (ART) fully suppresses the cycles of HIV replication and viral evolution in vivo. If replication persists in sanctuary sites such as the lymph nodes, a high priority should be placed on improving ART regimes to target these sites. To investigate the question of ongoing viral replication on current ART regimens, we analyzed HIV populations in longitudinal samples from 10 HIV-1-infected children who initiated ART when viral diversity was low. Eight children started ART at less than ten months of age and showed suppression of plasma viremia for seven to nine years. Two children had uncontrolled viremia for fifteen and thirty months, respectively, before viremia suppression, and served as positive controls for HIV replication and evolution. These latter 2 children showed clear evidence of virus evolution, whereas multiple methods of analysis bore no evidence of virus evolution in any of the 8 children with viremia suppression on ART. Phylogenetic trees simulated with the recently reported evolutionary rate of HIV-1 on ART of 6 215; 10-4 substitutions/site/month bore no resemblance to the observed data. Taken together, these data refute the concept that ongoing HIV replication is common with ART and is the major barrier to curing HIV-1 infection.

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External Sources

  1. DOI: 10.1172/JCI94582
  2. PMID: 28891813
  3. WOS: 000412017800027

Library Notes

  1. Fiscal Year: FY2016-2017
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