Antiretroviral Therapy for the Prevention of HIV-1 Transmission

Myron S. Cohen(University of North Carolina at Chapel Hill), Ying Qing Chen(University of North Carolina at Chapel Hill), Marybeth McCauley(University of North Carolina at Chapel Hill), Theresa Gamble(University of North Carolina at Chapel Hill), Mina C. Hosseinipour(University of North Carolina at Chapel Hill), Nagalingeswaran Kumarasamy(University of North Carolina at Chapel Hill), James Hakim(University of North Carolina at Chapel Hill), Johnstone Kumwenda(University of North Carolina at Chapel Hill), Beatriz Grinsztejn(University of North Carolina at Chapel Hill), José Henrique Pilotto(University of North Carolina at Chapel Hill), Sheela Godbole(University of North Carolina at Chapel Hill), Suwat Chariyalertsak(University of North Carolina at Chapel Hill), Breno Santos(University of North Carolina at Chapel Hill), Kenneth H. Mayer(University of North Carolina at Chapel Hill), Irving Hoffman(University of North Carolina at Chapel Hill), Susan H. Eshleman(University of North Carolina at Chapel Hill), Estelle Piwowar‐Manning(University of North Carolina at Chapel Hill), Leslie Cottle(University of North Carolina at Chapel Hill), Xinyi C. Zhang(University of North Carolina at Chapel Hill), Joseph Makhema(University of North Carolina at Chapel Hill), Lisa Mills(University of North Carolina at Chapel Hill), Ravindre Panchia(University of North Carolina at Chapel Hill), Sharlaa Faesen(University of North Carolina at Chapel Hill), Joseph J. Eron(University of North Carolina at Chapel Hill), Joel E. Gallant(University of North Carolina at Chapel Hill), Diane V. Havlir(University of North Carolina at Chapel Hill), Susan Swindells(University of North Carolina at Chapel Hill), Vanessa Elharrar(University of North Carolina at Chapel Hill), David Burns(University of North Carolina at Chapel Hill), Taha E. Taha(University of North Carolina at Chapel Hill), Karin Nielsen‐Saines(University of North Carolina at Chapel Hill), David D. Celentano(University of North Carolina at Chapel Hill), Max Essex(University of North Carolina at Chapel Hill), Sarah E. Hudelson(University of North Carolina at Chapel Hill), Andrew D. Redd(University of North Carolina at Chapel Hill), Thomas R. Fleming(University of North Carolina at Chapel Hill)
New England Journal of Medicine
July 18, 2016
Cited by 1,717Open Access
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Abstract

BACKGROUND: An interim analysis of data from the HIV Prevention Trials Network (HPTN) 052 trial showed that antiretroviral therapy (ART) prevented more than 96% of genetically linked infections caused by human immunodeficiency virus type 1 (HIV-1) in serodiscordant couples. ART was then offered to all patients with HIV-1 infection (index participants). The study included more than 5 years of follow-up to assess the durability of such therapy for the prevention of HIV-1 transmission. METHODS: We randomly assigned 1763 index participants to receive either early or delayed ART. In the early-ART group, 886 participants started therapy at enrollment (CD4+ count, 350 to 550 cells per cubic millimeter). In the delayed-ART group, 877 participants started therapy after two consecutive CD4+ counts fell below 250 cells per cubic millimeter or if an illness indicative of the acquired immunodeficiency syndrome (i.e., an AIDS-defining illness) developed. The primary study end point was the diagnosis of genetically linked HIV-1 infection in the previously HIV-1-negative partner in an intention-to-treat analysis. RESULTS: Index participants were followed for 10,031 person-years; partners were followed for 8509 person-years. Among partners, 78 HIV-1 infections were observed during the trial (annual incidence, 0.9%; 95% confidence interval [CI], 0.7 to 1.1). Viral-linkage status was determined for 72 (92%) of the partner infections. Of these infections, 46 were linked (3 in the early-ART group and 43 in the delayed-ART group; incidence, 0.5%; 95% CI, 0.4 to 0.7) and 26 were unlinked (14 in the early-ART group and 12 in the delayed-ART group; incidence, 0.3%; 95% CI, 0.2 to 0.4). Early ART was associated with a 93% lower risk of linked partner infection than was delayed ART (hazard ratio, 0.07; 95% CI, 0.02 to 0.22). No linked infections were observed when HIV-1 infection was stably suppressed by ART in the index participant. CONCLUSIONS: The early initiation of ART led to a sustained decrease in genetically linked HIV-1 infections in sexual partners. (Funded by the National Institute of Allergy and Infectious Diseases; HPTN 052 ClinicalTrials.gov number, NCT00074581 .).


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