US Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
Clin Infect Dis. 2021 Aug 2;73(3):e643-e651. doi: 10.1093/cid/ciaa1893.
Antiretroviral therapy (ART) initiation during acute and early human immunodeficiency virus infection (AEHI) limits HIV reservoir formation and may facilitate post-ART control but is logistically challenging. We evaluated the performance of AEHI diagnostic criteria from a prospective study of early ART initiation.
AIDS Clinical Trials Group A 5354 enrolled adults at 30 sites in the Americas, Africa, and Asia who met any 1 of 6 criteria based on combinations of results of HIV RNA, HIV antibody, Western blot or Geenius assay, and/or the signal-to-cutoff (S/CO) ratio of the ARCHITECT HIV Ag/Ab Combo or GS HIV Combo Ag/Ab EIA. HIV status and Fiebig stage were confirmed by centralized testing.
From 2017 through 2019, 195 participants were enrolled with median age of 27 years (interquartile range, 23-39). Thirty (15.4%) were female. ART was started by 171 (87.7%) on the day of enrollment and 24 (12.3%) the next day. AEHI was confirmed in 188 (96.4%) participants after centralized testing, 4 (2.0%) participants were found to have chronic infection, and 3 (1.5%) found not to have HIV discontinued ART and were withdrawn. Retrospectively, a nonreactive or indeterminate HIV antibody on the Geenius assay combined with ARCHITECT S/CO ≥10 correctly identified 99 of 122 (81.2%) Fiebig II-IV AEHI cases with no false-positive results.
Novel AEHI criteria that incorporate ARCHITECT S/CO facilitated rapid and efficient ART initiation without waiting for an HIV RNA result. These criteria may facilitate AEHI diagnosis, staging, and immediate ART initiation in future research studies and clinical practice.
NCT02859558.
在急性和早期人类免疫缺陷病毒感染(AEHI)期间启动抗逆转录病毒治疗(ART)可限制 HIV 储存库的形成,并可能有助于 ART 后的控制,但在后勤方面具有挑战性。我们评估了前瞻性早期 ART 启动研究中 AEHI 诊断标准的性能。
艾滋病临床治疗试验组 A 5354 在美洲、非洲和亚洲的 30 个地点招募符合以下 6 项标准之一的成年人:HIV RNA、HIV 抗体、Western blot 或 Geenius 检测以及/或 ARCHITECT HIV Ag/Ab Combo 或 GS HIV Combo Ag/Ab EIA 的信号与临界值(S/CO)比值的组合结果,和/或 HIV 状态和 Fiebig 分期通过集中检测确认。
2017 年至 2019 年,共招募了 195 名参与者,中位年龄为 27 岁(四分位间距,23-39)。30 名(15.4%)为女性。171 名(87.7%)参与者在入组当天开始接受 ART,24 名(12.3%)参与者在第二天开始接受 ART。经过集中检测,188 名(96.4%)参与者确诊为 AEHI,4 名(2.0%)参与者被发现患有慢性感染,3 名(1.5%)未感染 HIV 的参与者停止接受 ART 并被撤回。回顾性分析显示,Geenius 检测结果为非反应性或不确定的 HIV 抗体联合 ARCHITECT S/CO ≥10,可正确识别 122 例 Fiebig II-IV AEHI 病例中的 99 例(81.2%),无假阳性结果。
纳入 ARCHITECT S/CO 的新型 AEHI 标准可在不等待 HIV RNA 结果的情况下快速有效地启动 ART。这些标准可能有助于未来的研究和临床实践中的 AEHI 诊断、分期和立即启动 ART。
NCT02859558。