Antiretroviral Therapy Within 2 Years of HIV Acquisition Is Associated With Fewer Viral Blips: A Retrospective Analysis of More Than 20 Years of Data From the US Military HIV Natural History Study.
Trevor A Crowell, Hsing-Chuan Hsieh, Xun Wang, Xiuping Chu, Britt Gayle, Catherine M Berjohn, Jason M Blaylock, Joseph M Yabes, Derek T Larson, John H Powers, Robert J O'Connell, Anuradha Ganesan, Brian K Agan
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Abstract
Background: Viral blips have been associated with larger reservoir size and slower decay. Earlier antiretroviral therapy (ART) initiation may decrease the risk of blips.
Methods: We analyzed participants from the US Military HIV Natural History Study with an estimated human immunodeficiency virus (HIV) seroconversion date, viral suppression ≤400 copies/mL within 1 year after starting ART, and at least 3 HIV RNA measurements after suppression. A blip was defined as HIV RNA 401-1000 copies/mL preceded and followed by HIV RNA ≤400 copies/mL without changing ART. Cox proportional hazards models were used to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for factors potentially associated with the time from viral suppression to first blip.
Results: From 1996 through 2022, among 1413 participants on stable suppressive ART, 88 (6.2%) had at least one blip, including 68 (77.3%) with only a single blip. The overall incidence was 1.2 blips per 100 person-years (95% CI: .9-1.4). In multivariable modeling, ART initiation within 24 months of estimated HIV acquisition was independently associated with decreased hazard of viral blips compared with ART initiation after more than 24 months (0-6 months HR: 0.29 and 95% CI: .18-.48; 6-12 months HR: 0.43 and 95% CI: .31-.59; 12-24 months HR: 0.46 and 95% CI: .35-.60).
Conclusions: Participants who initiated ART within 2 years of HIV acquisition had lower hazard of blips, potentially reflecting smaller reservoir size and suggesting reservoir plasticity that extends beyond the acute phase of HIV.
病毒突变与较大的病毒库大小和较慢的病毒衰变有关。早期开始抗逆转录病毒治疗(ART)可能会降低突变的风险。方法:我们分析了来自美国军事HIV自然历史研究的参与者,他们估计了HIV血清转化日期,开始抗逆转录病毒治疗后1年内病毒抑制≤400拷贝/mL,抑制后至少3次HIV RNA测量。在不改变抗逆转录病毒治疗的情况下,HIV RNA 401-1000拷贝/mL为短暂现象,HIV RNA≤400拷贝/mL为短暂现象。Cox比例风险模型用于估计从病毒抑制到第一次发作的时间可能相关因素的风险比(hr)和95%置信区间(ci)。结果:从1996年到2022年,1413名接受稳定抑制性抗逆转录病毒治疗的参与者在HIV诊断时的中位年龄为29.2岁(四分位数间距为24.9-35.4岁),其中1361名(96.3%)为男性。在88名(6.2%)参与者中观察到病毒突变,其中68名(77.3%)只有一次突变。总发病率为每100人年1.2个点(95% CI 0.9-1.4)。在多变量模型中,与超过24个月后开始抗逆转录病毒治疗相比,在估计感染艾滋病毒的24个月内开始抗逆转录病毒治疗与病毒突变风险降低独立相关(0-6个月HR 0.29 [95% CI 0.18-0.48];6-12个月HR 0.43 [95% CI 0.31-0.59];12-24个月HR 0.46 [95% CI 0.35-0.60])。结论:在感染艾滋病毒两年内开始抗逆转录病毒治疗的参与者出现突变的风险较低,这可能反映了更小的病毒库规模,并表明病毒库的可塑性超出了艾滋病毒急性期。
期刊介绍:
Clinical Infectious Diseases (CID) is dedicated to publishing original research, reviews, guidelines, and perspectives with the potential to reshape clinical practice, providing clinicians with valuable insights for patient care. CID comprehensively addresses the clinical presentation, diagnosis, treatment, and prevention of a wide spectrum of infectious diseases. The journal places a high priority on the assessment of current and innovative treatments, microbiology, immunology, and policies, ensuring relevance to patient care in its commitment to advancing the field of infectious diseases.