Eshleman Susan H, Wilson Ethan A, Zhang Xinyi C, Ou San-San, Piwowar-Manning Estelle, Eron Joseph J, McCauley Marybeth, Gamble Theresa, Gallant Joel E, Hosseinipour Mina C, Kumarasamy Nagalingeswaran, Hakim James G, Kalonga Ben, Pilotto Jose H, Grinsztejn Beatriz, Godbole Sheela V, Chotirosniramit Nuntisa, Santos Breno Riegel, Shava Emily, Mills Lisa A, Panchia Ravindre, Mwelase Noluthando, Mayer Kenneth H, Chen Ying Q, Cohen Myron S, Fogel Jessica M
a Department of Pathology , Johns Hopkins University School of Medicine , Baltimore , MD , USA.
b Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center , Seattle , WA , USA.
HIV Clin Trials. 2017 May;18(3):100-109. doi: 10.1080/15284336.2017.1311056. Epub 2017 Apr 7.
The HIV Prevention Trials Network (HPTN) 052 trial demonstrated that early antiretroviral therapy (ART) prevented 93% of HIV transmission events in serodiscordant couples. Some linked infections were observed shortly after ART initiation or after virologic failure.
To evaluate factors associated with time to viral suppression and virologic failure in participants who initiated ART in HPTN 052.
1566 participants who had a viral load (VL) > 400 copies/mL at enrollment were included in the analyses. This included 832 in the early ART arm (CD4 350-550 cells/mm at ART initiation) and 734 in the delayed ART arm (204 with a CD4 < 250 cells/mm at ART initiation; 530 with any CD4 at ART initiation). Viral suppression was defined as two consecutive VLs ≤ 400 copies/mL after ART initiation; virologic failure was defined as two consecutive VLs > 1000 copies/mL > 24 weeks after ART initiation.
Overall, 93% of participants achieved viral suppression by 12 months. The annual incidence of virologic failure was 3.6%. Virologic outcomes were similar in the two study arms. Longer time to viral suppression was associated with younger age, higher VL at ART initiation, and region (Africa vs. Asia). Virologic failure was strongly associated with younger age, lower educational level, and lack of suppression by three months; lower VL and higher CD4 at ART initiation were also associated with virologic failure.
Several clinical and demographic factors were identified that were associated with longer time to viral suppression and virologic failure. Recognition of these factors may help optimize ART for HIV treatment and prevention.
艾滋病预防试验网络(HPTN)052试验表明,早期抗逆转录病毒疗法(ART)可预防93%的血清学不一致伴侣间的HIV传播事件。在开始ART后不久或病毒学失败后观察到了一些关联感染。
评估HPTN 052中开始接受ART治疗的参与者实现病毒抑制时间和病毒学失败的相关因素。
纳入1566名入组时病毒载量(VL)>400拷贝/mL的参与者进行分析。其中包括早期ART组的832人(开始ART时CD4为350 - 550个细胞/mm³)和延迟ART组的734人(开始ART时204人CD4<250个细胞/mm³;530人开始ART时CD4为任意值)。病毒抑制定义为开始ART后连续两次VL≤400拷贝/mL;病毒学失败定义为开始ART后24周连续两次VL>1000拷贝/mL。
总体而言,93%的参与者在12个月时实现了病毒抑制。病毒学失败的年发生率为3.6%。两个研究组的病毒学结果相似。实现病毒抑制的时间较长与年龄较小、开始ART时VL较高以及地区(非洲与亚洲)有关。病毒学失败与年龄较小、教育水平较低以及三个月时未实现抑制密切相关;开始ART时VL较低和CD4较高也与病毒学失败有关。
确定了几个与实现病毒抑制时间较长和病毒学失败相关的临床和人口统计学因素。认识这些因素可能有助于优化HIV治疗和预防的ART方案。