4.8 Article

Prevention of HIV-1 Infection with Early Antiretroviral Therapy

期刊

NEW ENGLAND JOURNAL OF MEDICINE
卷 365, 期 6, 页码 493-505

出版社

MASSACHUSETTS MEDICAL SOC
DOI: 10.1056/NEJMoa1105243

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资金

  1. National Institute of Allergy and Infectious Diseases
  2. National Institute of Allergy and Infectious Diseases [UM1-AI068619, U01-AI068619, UM1-AI068613, U01-AI068613, UM1-AI068617, U01-AI068617]
  3. Abbott Virology
  4. Roche Diagnostics
  5. Monogram Biosciences
  6. Sanofi Pasteur
  7. Merck
  8. Bristol-Myers Squibb
  9. GlaxoSmithKline
  10. ViiV Healthcare
  11. Gilead Sciences and Tibotec
  12. Roche
  13. Tibotec Therapeutics
  14. Pfizer
  15. Sangamo BioSciences
  16. Koronis

向作者/读者索取更多资源

Background Antiretroviral therapy that reduces viral replication could limit the transmission of human immunodeficiency virus type 1 (HIV-1) in serodiscordant couples. Methods In nine countries, we enrolled 1763 couples in which one partner was HIV-1-positive and the other was HIV-1-negative; 54% of the subjects were from Africa, and 50% of infected partners were men. HIV-1-infected subjects with CD4 counts between 350 and 550 cells per cubic millimeter were randomly assigned in a 1: 1 ratio to receive antiretroviral therapy either immediately (early therapy) or after a decline in the CD4 count or the onset of HIV-1-related symptoms (delayed therapy). The primary prevention end point was linked HIV-1 transmission in HIV-1-negative partners. The primary clinical end point was the earliest occurrence of pulmonary tuberculosis, severe bacterial infection, a World Health Organization stage 4 event, or death. Results As of February 21, 2011, a total of 39 HIV-1 transmissions were observed (incidence rate, 1.2 per 100 person-years; 95% confidence interval [CI], 0.9 to 1.7); of these, 28 were virologically linked to the infected partner (incidence rate, 0.9 per 100 person-years, 95% CI, 0.6 to 1.3). Of the 28 linked transmissions, only 1 occurred in the early-therapy group (hazard ratio, 0.04; 95% CI, 0.01 to 0.27; P<0.001). Subjects receiving early therapy had fewer treatment end points (hazard ratio, 0.59; 95% CI, 0.40 to 0.88; P = 0.01). Conclusions The early initiation of antiretroviral therapy reduced rates of sexual transmission of HIV-1 and clinical events, indicating both personal and public health benefits from such therapy.

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