Department of Medicine, University of Washington, Seattle, WA.
Department of Epidemiology, University of Washington, Seattle, WA.
J Acquir Immune Defic Syndr. 2022 Apr 15;89(5):537-545. doi: 10.1097/QAI.0000000000002902.
Point-of-care (POC) nucleic acid tests (NATs) have potential to diagnose acute HIV infection and monitor persons taking pre-exposure prophylaxis or antiretroviral therapy (ART). POC NATs have not yet been evaluated in the US.
From June 2018-March 2019, we conducted a cross-sectional evaluation of the Simple Amplification-Based Assay version II (SAMBA II) POC NAT. People with HIV (PWH) and persons testing for HIV were tested with the SAMBA II qualitative (Qual) whole blood (WB) test. From April-September 2019, the Qual test was used on persons who were ART-naive, and SAMBA II Semi-quantitative (Semi-Q) WB was used with ART-experienced PWH. Both were performed on unprocessed venipuncture (VP) and, when indicated by protocol, fingerstick (FS) WB and plasma. SAMBA results were compared with Abbott RealTime HIV-1 polymerase chain reaction results on plasma. We calculated sensitivity, specificity, and concordance between tests.
SAMBA was used in 330 visits among 280 participants: 202 (61.2%) visits from PWH, and 128 (38.8%) from HIV-negative persons. Qual test sensitivity with ART-naive participants was 91.4% [32/35, 95% confidence interval (CI): 77.6% to 97.0%] using VP WB and 100% (27/27, 95% CI: 87.5% to 100%) using FS WB. Specificity was 100% using both specimen types. Concordance between the gold standard and Semi-Q at 1000 copies/mL among PWH on ART was 97.7% (86/88, 95% CI: 92.1% to 99.4%) and 100% (30/30, 95% CI: 88.7% to 100%) using VP and FS WB, respectively.
The SAMBA II POC NATs showed high sensitivity, specificity, and concordance with the gold standard assay, indicating its potential use in diagnostics and monitoring. Future work will evaluate POC NAT implementation in the US.
即时检测(POC)核酸检测(NAT)有可能诊断急性 HIV 感染并监测接受暴露前预防或抗逆转录病毒治疗(ART)的人员。POC NAT 尚未在美国进行评估。
从 2018 年 6 月至 2019 年 3 月,我们对即时检测基于简单扩增的分析 II 版(SAMBA II)POC NAT 进行了横断面评估。HIV 感染者(PWH)和 HIV 检测者接受 SAMBA II 定性(Qual)全血(WB)检测。从 2019 年 4 月至 9 月,Qual 检测用于初治接受 ART 的人员,SAMBA II 半定量(Semi-Q)WB 用于接受 ART 的 PWH。两者均在未经处理的静脉穿刺(VP)以及根据方案指示的指尖采血(FS)WB 和血浆上进行。SAMBA 结果与 Abbott RealTime HIV-1 聚合酶链反应结果在血浆上进行比较。我们计算了检测之间的灵敏度、特异性和一致性。
SAMBA 用于 280 名参与者的 330 次就诊:202 次就诊来自 PWH,128 次就诊来自 HIV 阴性者。在初治接受 ART 的参与者中,Qual 检测的灵敏度为 91.4%[32/35,95%置信区间(CI):77.6%至 97.0%],VP WB 为 100%(27/27,95%CI:87.5%至 100%),FS WB 为 100%。两种标本类型的特异性均为 100%。在接受 ART 的 PWH 中,金标准与 Semi-Q 在 1000 拷贝/mL 时的一致性分别为 97.7%(86/88,95%CI:92.1%至 99.4%)和 100%(30/30,95%CI:88.7%至 100%),VP 和 FS WB 分别为 97.7%和 100%。
SAMBA II POC NAT 与金标准检测具有高灵敏度、特异性和一致性,表明其在诊断和监测方面具有潜在用途。未来的工作将评估 POC NAT 在美