HIV-1 genital shedding in HIV-infected patients randomized to second-line lopinavir/ritonavir monotherapy versus tenofovir/lamivudine/lopinavir/ritonavir

HIV-1 shedding in genital secretions is associated with HIV transmission risk. Limited data exist on the effect of second-line lopinavir/ritonavir monotherapy (mLPV/r) on genital secretion of HIV RNA. We measured HIV-1 in genital secretions of HIV-infected adults at time of failure from non-nucleosi...

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Veröffentlicht in:Antiviral therapy 2014-01, Vol.19 (6), p.579-586
Hauptverfasser: Bunupuradah, Torsak, Bowonwattanuwong, Chureeratana, Jirajariyavej, Supunnee, Munsakul, Warangkana, Klinbuayaem, Virat, Sophonphan, Jiratchaya, Mahanontharit, Apicha, Hirschel, Bernard, Ruxrungtham, Kiat, Ananworanich, Jintanat
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Sprache:eng
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Zusammenfassung:HIV-1 shedding in genital secretions is associated with HIV transmission risk. Limited data exist on the effect of second-line lopinavir/ritonavir monotherapy (mLPV/r) on genital secretion of HIV RNA. We measured HIV-1 in genital secretions of HIV-infected adults at time of failure from non-nucleoside reverse transcriptase inhibitor (NNRTI)-based regimens and at 48 weeks after being randomized to second-line mLPV/r versus tenofovir/lamivudine/LPV/r (TDF/3TC/LPV/r). Plasma and genital secretion (semen, vaginal swab) HIV RNA was quantified by the CobasAmpliprep/TaqMan assay. Forty enrolled (15 on mLPV/r and 25 on TDF/3TC/LPV/r). Median age was 37.8 years and 35% were male. Median baseline CD4(+) T-cell count was 222 cells/mm(3), plasma HIV RNA was 4.1 log10 copies/ml and genital secretion HIV RNA was 2.3 log10 copies/ml. At week 48, the proportion of patients with plasma HIV RNA50 copies/ml at week 48 was baseline genital secretion HIV RNA>50 copies/ml (P=0.049). LPV/r either given alone or in combination with TDF/3TC as second-line treatment achieved high genital secretion HIV RNA suppression rate. Genital secretion HIV RNA remained detectable at low levels in one-third of patients with suppressed plasma viraemia.
ISSN:1359-6535
2040-2058
DOI:10.3851/IMP2737