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Risk of drug resistance among persons acquiring HIV within a randomized clinical trial of single-or dual-agent preexposure prophylaxis

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dc.contributor.author Lehman, Dara A.
dc.contributor.author Baeten, Jared M.
dc.contributor.author McCoy, Connor O.
dc.contributor.author Weis, Julie F.
dc.contributor.author Peterson, Dylan
dc.contributor.author Mbara, Gerald
dc.contributor.author Donnell, Deborah
dc.contributor.author Thomas, Katherine K.
dc.contributor.author Hendrix, Craig W.
dc.contributor.author Marzinke, Mark A.
dc.contributor.author Frenkel, Lisa
dc.contributor.author Ndase, Patrick
dc.contributor.author Mugo, Nelly R.
dc.contributor.author Celum, Connie
dc.contributor.author Overbaugh, Julie
dc.contributor.author Were, Edwin
dc.date.accessioned 2021-07-12T08:36:02Z
dc.date.available 2021-07-12T08:36:02Z
dc.date.issued 2015
dc.identifier.uri https://doi.org/10.1093/infdis/jiu677
dc.identifier.uri http://ir.mu.ac.ke:8080/jspui/handle/123456789/4829
dc.description.abstract Background. Preexposure prophylaxis (PrEP) with emtricitabine plus tenofovir disoproxil fumarate (FTC/TDF) or TDF alone reduces the risk of human immunodeficiency virus (HIV) acquisition. Understanding the risk of antiretroviral resistance selected by PrEP during breakthrough infections is important because of the risk of treatment failure during subsequent antiretroviral use. Methods. Within the largest randomized trial of FTC/TDF versus TDF as PrEP, plasma samples were tested for HIV with resistance mutations associated with FTC (K65R and M184IV) and TDF (K65R and K70E), using 454 sequencing. Results. Of 121 HIV seroconverters, 25 received FTC/TDF, 38 received TDF, and 58 received placebo. Plasma drug levels in 26 individuals indicated PrEP use during or after HIV acquisition, of which 5 had virus with resistance mutations associated with their PrEP regimen. Among those with PrEP drug detected during infection, resistance was more frequent in the FTC/TDF arm (4 of 7 [57%]), compared with the TDF arm (1 of 19 [5.3%]; P = .01), owing to the FTC-associated mutation M184IV. Of these cases, 3 had unrecognized acute infection at PrEP randomization, and 2 were HIV negative at enrollment. Conclusions. These results suggest that resistance selected by PrEP is rare but can occur both with PrEP initiation during acute seronegative HIV infection and in PrEP breakthrough infections and that FTC is associated with a greater frequency of resistance mutations than TDF. en_US
dc.language.iso en en_US
dc.publisher Oxford university press en_US
dc.subject Drug resistance en_US
dc.subject Pre-exposure prophylaxis en_US
dc.subject Antiretroviral resistance en_US
dc.subject HIV prevention en_US
dc.title Risk of drug resistance among persons acquiring HIV within a randomized clinical trial of single-or dual-agent preexposure prophylaxis en_US
dc.type Article en_US


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