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Background
Antiretroviral preexposure prophylaxis is a promising approach for preventing human
immunodeficiency virus type 1 (HIV-1) infection in heterosexual populations.
Methods
We conducted a randomized trial of oral antiretroviral therapy for use as preexposure
prophylaxis among HIV-1–serodiscordant heterosexual couples from Kenya and
Uganda. The HIV-1–seronegative partner in each couple was randomly assigned to
one of three study regimens — once-daily tenofovir (TDF), combination tenofovir–
emtricitabine (TDF–FTC), or matching placebo — and followed monthly for up to
36 months. At enrollment, the HIV-1–seropositive partners were not eligible for antiretroviral
therapy, according to national guidelines. All couples received standard
HIV-1 treatment and prevention services.
Results
We enrolled 4758 couples, of whom 4747 were followed: 1584 randomly assigned to
TDF, 1579 to TDF–FTC, and 1584 to placebo. For 62% of the couples followed, the
HIV-1–seronegative partner was male. Among HIV-1–seropositive participants, the
median CD4 count was 495 cells per cubic millimeter (interquartile range, 375 to 662).
A total of 82 HIV-1 infections occurred in seronegative participants during the study,
17 in the TDF group (incidence, 0.65 per 100 person-years), 13 in the TDF–FTC group
(incidence, 0.50 per 100 person-years), and 52 in the placebo group (incidence, 1.99
per 100 person-years), indicating a relative reduction of 67% in the incidence of
HIV-1 with TDF (95% confidence interval [CI], 44 to 81; P<0.001) and of 75% with
TDF–FTC (95% CI, 55 to 87; P<0.001). Protective effects of TDF–FTC and TDF alone
against HIV-1 were not significantly different (P = 0.23), and both study medications
significantly reduced the HIV-1 incidence among both men and women. The rate of
serious adverse events was similar across the study groups. Eight participants receiving
active treatment were found to have been infected with HIV-1 at baseline,
and among these eight, antiretroviral resistance developed in two during the study.
Conclusions
Oral TDF and TDF–FTC both protect against HIV-1 infection in heterosexual men
and women. (Funded by the Bill and Melinda Gates Foundation; Partners PrEP
ClinicalTrials.gov number, NCT00557245.) |
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