Prevention of HIV-1 Infection with Early Antiretroviral Therapy

被引:4762
|
作者
Cohen, Myron S. [1 ]
Chen, Ying Q. [2 ]
McCauley, Marybeth [4 ,5 ]
Gamble, Theresa
Hosseinipour, Mina C.
Kumarasamy, Nagalingeswaran [7 ]
Hakim, James G. [9 ]
Kumwenda, Johnstone [6 ]
Grinsztejn, Beatriz [10 ]
Pilotto, Jose H. S. [11 ,12 ]
Godbole, Sheela V. [8 ]
Mehendale, Sanjay [8 ]
Chariyalertsak, Suwat [13 ]
Santos, Breno R. [14 ]
Mayer, Kenneth H. [15 ]
Hoffman, Irving F.
Eshleman, Susan H. [17 ]
Piwowar-Manning, Estelle [17 ]
Wang, Lei [2 ]
Makhema, Joseph [19 ]
Mills, Lisa A. [20 ]
de Bruyn, Guy [21 ]
Sanne, Ian [22 ]
Eron, Joseph
Gallant, Joel [17 ]
Havlir, Diane [23 ]
Swindells, Susan [24 ]
Ribaudo, Heather [16 ]
Elharrar, Vanessa [25 ]
Burns, David [25 ]
Taha, Taha E. [18 ]
Nielsen-Saines, Karin [26 ]
Celentano, David [18 ]
Essex, Max [16 ]
Fleming, Thomas R. [3 ]
机构
[1] Univ N Carolina, Inst Global Hlth & Infect Dis, Sch Med, Chapel Hill, NC 27599 USA
[2] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Div, Seattle, WA 98104 USA
[3] Univ Washington, Seattle, WA 98195 USA
[4] Family Hlth Int, Arlington, VA USA
[5] Family Hlth Int, Durham, NC USA
[6] Johns Hopkins Project, Coll Med, Blantyre, Malawi
[7] YR Gaitonade Ctr AIDS Res & Educ, Chennai, Tamil Nadu, India
[8] Natl AIDS Res Inst, Pune, Maharashtra, India
[9] Univ Zimbabwe, Harare, Zimbabwe
[10] Fiocruz MS, Inst Pesquisa Clin Evandro Chagas, BR-21045900 Rio De Janeiro, Brazil
[11] Fiocruz MS, Hosp Geral de Nova Iguacu, BR-21045900 Rio De Janeiro, Brazil
[12] Lab AIDS & Imunol Mol IOC Fiocurz, BR-21045900 Rio De Janeiro, Brazil
[13] Chiang Mai Univ, Res Inst Hlth Sci, Chiang Mai 50000, Thailand
[14] Hosp Nossa Senhora da Conceicao, Porto Alegre, RS, Brazil
[15] Fenway Hlth, Boston, MA USA
[16] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[17] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[18] Johns Hopkins Bloomberg Sch Publ Hlth, Baltimore, MD USA
[19] Botswana Harvard AIDS Inst, Gaborone, Botswana
[20] Ctr Dis Control & Prevent CDC, Div HIV AIDS Prevent, Kenya Med Res Inst, CDC Res & Publ Hlth Collaborat HIV Res Branch, Kisumu, Kenya
[21] Univ Witwatersrand, Perinatal HIV Res Unit, Johannesburg, South Africa
[22] Univ Witwatersrand, Dept Med, ZA-2001 Johannesburg, South Africa
[23] Univ Calif San Francisco, San Francisco, CA 94143 USA
[24] Univ Nebraska Med Ctr, Omaha, NE USA
[25] NIAID, Div Aids, NIH, Bethesda, MD 20892 USA
[26] David Geffen UCLA Sch Med, Los Angeles, CA USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2011年 / 365卷 / 06期
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; HETEROSEXUAL TRANSMISSION; HIV-1-INFECTED PATIENTS; MORTALITY; INITIATION; RETHINKING; RATES; RISK;
D O I
10.1056/NEJMoa1105243
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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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收藏
页码:493 / 505
页数:13
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