Antiretroviral Prophylaxis for HIV Prevention in Heterosexual Men and Women

被引:2382
|
作者
Baeten, J. M. [1 ,2 ,3 ]
Donnell, D. [6 ]
Ndase, P.
Mugo, N. R. [9 ,10 ]
Campbell, J. D. [13 ]
Wangisi, J. [14 ]
Tappero, J. W. [17 ]
Bukusi, E. A. [9 ,10 ,11 ,18 ]
Cohen, C. R. [18 ]
Katabira, E. [15 ]
Ronald, A. [15 ,19 ]
Tumwesigye, E. [16 ]
Were, E. [12 ]
Fife, K. H. [20 ]
Kiarie, J. [9 ,10 ]
Farquhar, C. [2 ,3 ]
John-Stewart, G. [2 ,3 ]
Kakia, A. [14 ]
Odoyo, J. [11 ]
Mucunguzi, A. [14 ]
Nakku-Joloba, E. [15 ]
Twesigye, R. [16 ]
Ngure, K. [9 ,10 ]
Apaka, C. [12 ]
Tamooh, H. [9 ,10 ]
Gabona, F. [15 ]
Mujugira, A.
Panteleeff, D.
Thomas, K. K.
Kidoguchi, L.
Krows, M.
Revall, J.
Morrison, S.
Haugen, H.
Emmanuel-Ogier, M.
Ondrejcek, L. [7 ]
Coombs, R. W. [2 ,4 ]
Frenkel, L. [4 ,5 ,8 ]
Hendrix, C. [21 ]
Bumpus, N. N. [21 ]
Bangsberg, D. [22 ,23 ]
Haberer, J. E. [22 ,23 ]
Stevens, W. S. [24 ,25 ]
Lingappa, J. R. [2 ,5 ]
Celum, C. [2 ,3 ]
机构
[1] Univ Washington, Dept Global Hlth, Int Clin Res Ctr, Seattle, WA 98104 USA
[2] Univ Washington, Dept Med, Seattle, WA 98104 USA
[3] Univ Washington, Dept Epidemiol, Seattle, WA 98104 USA
[4] Univ Washington, Dept Lab Med, Seattle, WA 98104 USA
[5] Univ Washington, Dept Pediat, Seattle, WA 98104 USA
[6] Fred Hutchinson Canc Res Ctr, Stat Ctr HIV AIDS Res & Prevent, Seattle, WA 98104 USA
[7] DF Net Res, Seattle, WA USA
[8] Seattle Childrens Hosp Res Inst, Seattle, WA USA
[9] Univ Nairobi, Dept Obstet & Gynecol, Nairobi, Kenya
[10] Kenyatta Natl Hosp, Nairobi, Kenya
[11] Kenya Govt Med Res Ctr, Ctr Microbiol Res, Nairobi, Kenya
[12] Moi Univ, Dept Reprod Hlth, Eldoret, Kenya
[13] Ctr Dis Control & Prevent, Entebbe, Uganda
[14] Makerere Univ, AIDS Support Org, Kampala, Uganda
[15] Makerere Univ, Infect Dis Inst, Kampala, Uganda
[16] Kabwohe Clin Res Ctr, Kabwohe, Uganda
[17] Ctr Dis Control & Prevent, Atlanta, GA USA
[18] Univ Calif San Francisco, Dept Obstet Gynecol & Reprod Sci, San Francisco, CA USA
[19] Univ Manitoba, Dept Med, Winnipeg, MB, Canada
[20] Indiana Univ, Dept Med, Indianapolis, IN USA
[21] Johns Hopkins Univ, Dept Med, Baltimore, MD USA
[22] Massachusetts Gen Hosp, Boston, MA 02114 USA
[23] Harvard Univ, Sch Med, Boston, MA USA
[24] Univ Witwatersrand, Dept Mol Med & Hematol, Johannesburg, South Africa
[25] Wits Hlth Consortium, Contract Lab Serv, Johannesburg, South Africa
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2012年 / 367卷 / 05期
关键词
SUB-SAHARAN AFRICA; PREEXPOSURE PROPHYLAXIS; SEXUAL TRANSMISSION; VIRAL LOAD; THERAPY; INFECTION; ADHERENCE; COUPLES;
D O I
10.1056/NEJMoa1108524
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.)
引用
收藏
页码:399 / 410
页数:12
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