HIV Pathogenesis Section, NIAID/NIH, Bethesda, MD.
Infectious Diseases, Weill Cornell Medicine, Weill Cornell Medical College, Cornell University, New York, NY.
J Acquir Immune Defic Syndr. 2019 Aug 1;81(4):456-462. doi: 10.1097/QAI.0000000000002052.
The benefit of immediate antiretroviral therapy (ART) at CD4 >500 cells/μL was established in the Strategic Timing of Antiretroviral Treatment (START) study. The benefits and risks of immediate ART in participants with low pretreatment viremia, including virologic suppressors, were further assessed.
Randomized prospective international study.
START participants with enrollment viremia <3000 c/mL were included. We compared clinical outcomes (grade 4 adverse events, hospitalizations, or death), plasma viremia, CD4 counts, and changes in biomarkers in immediate versus deferred ART groups.
Participants (N = 1134 including 93 with viremia ≤50 c/mL) had a median age of 37 years, 40% were women, and median CD4 was 713 cells/µL. Ninety-seven percent in the immediate and 29% in the deferred arm initiated ART at a median of 6 and 699 days, respectively. Clinical outcomes were experienced in 64 versus 61 patients in immediate and deferred arms (hazard ratio 1.10, 95% confidence interval: 0.77 to 1.56). The CD4 count difference was 125 cells/µL at 12 and 235 cells/µL at 36 months higher in the immediate versus deferred groups. D-dimer and VCAM levels decreased, and C-reactive protein increased, in the immediate arm at month 8. No significant changes in CD4 counts or biomarkers were observed in persons who maintained spontaneous virologic suppression.
START participants with low enrollment viremia experienced higher CD4 counts, greater proportion with suppressed viremia, and decreases in D-dimer levels on immediate ART despite the lack of difference in serious clinical outcomes. These data support immediate ART in people with low viremia, although equipoise remains for suppressors.
在战略时机启动抗逆转录病毒治疗(START)研究中,CD4 细胞>500 个/μL 时开始抗逆转录病毒治疗(ART)的益处已得到确立。进一步评估了低预处理病毒血症(包括病毒学抑制者)参与者中立即开始 ART 的益处和风险。
随机前瞻性国际研究。
纳入了开始研究中入组时病毒载量<3000 c/mL 的参与者。我们比较了即刻 ART 组与延迟 ART 组的临床结局(4 级不良事件、住院或死亡)、血浆病毒载量、CD4 计数以及生物标志物的变化。
共有 1134 名参与者(包括病毒载量≤50 c/mL 的 93 名参与者),其平均年龄为 37 岁,40%为女性,平均 CD4 为 713 个/μL。即刻 ART 组和延迟 ART 组分别有 97%和 29%的患者在中位时间 6 天和 699 天后开始接受 ART。即刻和延迟 ART 组中各有 64 名和 61 名患者发生临床结局(风险比 1.10,95%置信区间:0.77 至 1.56)。即刻 ART 组和延迟 ART 组在 12 个月和 36 个月时的 CD4 计数差异分别为 125 个/μL 和 235 个/μL。在第 8 个月,即刻治疗组的 D-二聚体和 VCAM 水平下降,C 反应蛋白升高。在维持自发病毒学抑制的患者中,未观察到 CD4 计数或生物标志物的显著变化。
在开始研究中病毒载量较低的参与者中,尽管严重临床结局无差异,但 CD4 计数较高,更多的患者病毒载量被抑制,D-二聚体水平下降。这些数据支持低病毒血症患者进行即刻 ART,尽管抑制者仍存在均衡性。