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Antiretroviral preexposure prophylaxis for heterosexual HIV transmission in Botswana

  • Michael C. Thigpen
  • , Poloko M. Kebaabetswe
  • , Lynn A. Paxton
  • , Dawn K. Smith
  • , Charles E. Rose
  • , Tebogo M. Segolodi
  • , Faith L. Henderson
  • , Sonal R. Pathak
  • , Fatma A. Soud
  • , Kata L. Chillag
  • , Rodreck Mutanhaurwa
  • , Lovemore Ian Chirwa
  • , Michael Kasonde
  • , Daniel Abebe
  • , Evans Buliva
  • , Roman J. Gvetadze
  • , Sandra Johnson
  • , Thom Sukalac
  • , Vasavi T. Thomas
  • , Clyde Hart
  • Jeffrey A. Johnson, C. Kevin Malotte, Craig W. Hendrix, John T. Brooks

Research output: Contribution to journal › Article › peer-review

Abstract

BACKGROUND: Preexposure prophylaxis with antiretroviral agents has been shown to reduce the transmission of human immunodeficiency virus (HIV) among men who have sex with men; however, the efficacy among heterosexuals is uncertain. METHODS:We randomly assigned HIV-seronegative men and women to receive either tenofovir disoproxil fumarate and emtricitabine (TDF-FTC) or matching placebo once daily. Monthly study visits were scheduled, and participants received a comprehensive package of prevention services, including HIV testing, counseling on adherence to medication, management of sexually transmitted infections, monitoring for adverse events, and individualized counseling on risk reduction; bone mineral density testing was performed semiannually in a subgroup of participants. RESULTS:A total of 1219 men and women underwent randomization (45.7% women) and were followed for 1563 person-years (median, 1.1 years; maximum, 3.7 years). Because of low retention and logistic limitations, we concluded the study early and followed enrolled participants through an orderly study closure rather than expanding enrollment. The TDF-FTC group had higher rates of nausea (18.5% vs. 7.1%, P<0.001), vomiting (11.3% vs. 7.1%, P = 0.008), and dizziness (15.1% vs. 11.0%, P = 0.03) than the placebo group, but the rates of serious adverse events were similar (P = 0.90). Participants who received TDF-FTC, as compared with those who received placebo, had a significant decline in bone mineral density. K65R, M184V, and A62V resistance mutations developed in 1 participant in the TDF-FTC group who had had an unrecognized acute HIV infection at enrollment. In a modified intention-to-treat analysis that included the 33 participants who became infected during the study (9 in the TDF-FTC group and 24 in the placebo group; 1.2 and 3.1 infections per 100 person-years, respectively), the efficacy of TDF-FTC was 62.2% (95% confidence interval, 21.5 to 83.4; P = 0.03). CONCLUSIONS:Daily TDF-FTC prophylaxis prevented HIV infection in sexually active heterosexual adults. The long-term safety of daily TDF-FTC prophylaxis, including the effect on bone mineral density, remains unknown. (Funded by the Centers for Disease Control and Prevention and the National Institutes of Health; TDF2 ClinicalTrials.gov number, NCT00448669.)

Original languageEnglish (US)
Pages (from-to)423-434
Number of pages12
JournalNew England Journal of Medicine
Volume367
Issue number5
DOIs
StatePublished - Aug 2 2012

ASJC Scopus subject areas

  • General Medicine

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