
Treatment intensification does not reduce residual HIV-1 viremia in patients on highly active antiretroviral therapy
Author(s) -
Jason B. Dinoso,
S. Y. Kim,
Ann Wiegand,
Sarah Palmer,
Stephen J. Gange,
Lisa M. Cranmer,
Angeline O'Shea,
Marc Callender,
Adam M. Spivak,
Timothy Brennan,
Mary F. Kearney,
Michael A. Proschan,
JoAnn M. Mican,
Catherine Rehm,
John M. Coffin,
John W. Mellors,
Robert F. Siliciano,
Frank Maldarelli
Publication year - 2009
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0903107106
Subject(s) - viremia , virology , efavirenz , viral load , ritonavir , lopinavir , viral replication , biology , immunology , medicine , antiretroviral therapy , virus
In HIV-1-infected individuals on currently recommended antiretroviral therapy (ART), viremia is reduced to <50 copies of HIV-1 RNA per milliliter, but low-level residual viremia appears to persist over the lifetimes of most infected individuals. There is controversy over whether the residual viremia results from ongoing cycles of viral replication. To address this question, we conducted 2 prospective studies to assess the effect of ART intensification with an additional potent drug on residual viremia in 9 HIV-1-infected individuals on successful ART. By using an HIV-1 RNA assay with single-copy sensitivity, we found that levels of viremia were not reduced by ART intensification with any of 3 different antiretroviral drugs (efavirenz, lopinavir/ritonavir, or atazanavir/ritonavir). The lack of response was not associated with the presence of drug-resistant virus or suboptimal drug concentrations. Our results suggest that residual viremia is not the product of ongoing, complete cycles of viral replication, but rather of virus output from stable reservoirs of infection.
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