Mujugira Andrew, Celum Connie, Coombs Robert W, Campbell James D, Ndase Patrick, Ronald Allan, Were Edwin, Bukusi Elizabeth A, Mugo Nelly, Kiarie James, Baeten Jared M
Departments of *Global Health; †Epidemiology; ‡Medicine; §Laboratory Medicine, University of Washington, Seattle, WA; ‖Division of Infectious Diseases and Tropical Pediatrics, University of Maryland, Baltimore, MD; ¶Department of Medicine, University of Manitoba, Winnipeg, Canada; #Department of Medical Microbiology, University of Manitoba, Winnipeg, Canada; **Department of Reproductive Health, Moi University, Eldoret, Kenya; ††Center for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya; ‡‡Center for Clinical Research, Kenya Medical Research Institute, Nairobi, Kenya; and §§Department of Reproductive Health and Research, World Health Organization, Geneva, Switzerland.
J Acquir Immune Defic Syndr. 2016 Aug 15;72(5):579-84. doi: 10.1097/QAI.0000000000001019.
Combination antiretroviral therapy (ART) decreases the risk of sexual HIV transmission by suppressing blood and genital HIV RNA concentrations. We sought to determine HIV transmission risk prior to achieving complete viral suppression.
Prospective cohort study.
Using data from the Partners PrEP Study, a prospective study of 4747 heterosexual HIV-serodiscordant couples in Kenya and Uganda, we examined multiple markers of HIV transmission risk during the first months after ART initiation: time to viral suppression in blood, persistence of HIV RNA in genital specimens, sexual risk behavior, pregnancy incidence, and HIV transmission using survival analysis and generalized estimating equations logistic regression.
The cumulative probabilities of achieving blood viral suppression (<80 copies per milliliter) 3, 6, and 9 months after ART initiation were 65.3%, 84.8%, and 89.1%, respectively. Endocervical and seminal HIV RNA were detectable in 12% and 21% of samples obtained within 6 months of ART. Pregnancy incidence was 8.8 per 100 person-years during the first 6 months of ART, and sex unprotected by condoms was reported at 10.5% of visits. Among initially uninfected partners, HIV incidence before ART was 2.08 per 100 person-years (55 infections; 2644 person-years), 1.79 for 0-6 months after ART initiation (3 infections; 168 person-years), and 0.00 with >6 months of ART (0 infections; 167 person-years).
Residual HIV transmission risk persists during the first 6 months of ART, with incomplete viral suppression in blood and genital compartments. For HIV-serodiscordant couples in which the infected partner starts ART, other prevention options are needed, such as pre-exposure prophylaxis, until viral suppression is achieved.
联合抗逆转录病毒疗法(ART)通过抑制血液和生殖器中的HIV RNA浓度来降低性传播HIV的风险。我们试图确定在实现完全病毒抑制之前的HIV传播风险。
前瞻性队列研究。
利用来自“伴侣PrEP研究”的数据,这是一项对肯尼亚和乌干达4747对异性恋HIV血清学不一致夫妇的前瞻性研究,我们在开始ART后的头几个月内检查了HIV传播风险的多个指标:血液中病毒抑制的时间、生殖器标本中HIV RNA的持续存在、性风险行为、妊娠发生率以及使用生存分析和广义估计方程逻辑回归分析HIV传播情况。
开始ART后3、6和9个月实现血液病毒抑制(<80拷贝/毫升)的累积概率分别为65.3%、84.8%和89.1%。在开始ART后6个月内采集的样本中,分别有12%和21%的样本可检测到宫颈内和精液中的HIV RNA。在ART的前6个月,妊娠发生率为每100人年8.8例,在10.5%的就诊中报告有未使用避孕套的性行为。在最初未感染的伴侣中,ART前HIV发病率为每100人年2.08例(55例感染;2644人年),ART开始后0至6个月为每100人年1.79例(3例感染;168人年),ART超过6个月后为0.00例(0例感染;167人年)。
在ART的前6个月中,由于血液和生殖器部位的病毒抑制不完全,HIV传播风险仍然存在。对于感染伴侣开始ART的HIV血清学不一致夫妇,在实现病毒抑制之前,需要其他预防措施,如暴露前预防。