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Intrapartum Tenofovir and Emtricitabine Reduces Low-Concentration Drug Resistance Selected by Single-Dose Nevirapine for Perinatal HIV Prevention

Authors :
Elizabeth M. Stringer
Ronald A. Cantrell
Ranjit Warrier
Giovanina M. Ellis
Benjamin H. Chi
Kyle J. Nakamura
Felistas Mbewe
Moses Sinkala
Namwinga Chintu
Jeffrey S. A. Stringer
Grace M. Aldrovandi
Lisa M. Frenkel
Source :
AIDS Research and Human Retroviruses. 25:1099-1106
Publication Year :
2009
Publisher :
Mary Ann Liebert Inc, 2009.

Abstract

A single dose of tenofovir/emtricitabine (TDF/FTC) during labor significantly reduces peripartum nevirapine-associated viral drug resistance when measured by consensus HIV sequencing. It is unknown whether this effect extends to HIV subpopulations of25-50%. We conducted a randomized trial of single-dose TDF/FTC added to peripartum nevirapine to reduce drug resistance associated with nonnucleoside reverse transcriptase inhibitors (NNRTIs). To detect mutations for NNRTIs comprisingor = 2% of the viral population, we used an oligonucleotide ligation assay (OLA) at codons 103, 106, 181, and 190 of HIV reverse transcriptase. To assess development of drug resistance mutations to our study intervention, OLA was also performed at codons 65 and 184. Among the 328 women included in the 2-week analysis, those receiving TDF/FTC were less likely to have NNRTI resistance by OLA (RR = 0.40, 95% CI = 0.21-0.77). A similar trend was observed among the 315 women included in the 6-week analysis (RR = 0.45, 95% CI = 0.31-0.66). Only two (1%) specimens had detectable K65R by OLA. Both were at 6 weeks postpartum; one was detected in the intervention arm and one in the control arm (p = 0.96). M184V was not detected. The ability of single-dose TDF/FTC to protect against peripartum NVP-induced NNRTI resistance extends to minority populations. This efficacy is achieved without significant selection of TDF- or FTC-resistant viruses.

Details

ISSN :
19318405 and 08892229
Volume :
25
Database :
OpenAIRE
Journal :
AIDS Research and Human Retroviruses
Accession number :
edsair.doi.dedup.....5a275505adc67caa26feb7540b69c8ee