Yufenyuy Ernest L, Detorio Mervi, Dobbs Trudy, Patel Hetal K, Jackson Keisha, Vedapuri Shanmugam, Parekh Bharat S
Division of Global HIV and TB, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
PLOS Glob Public Health. 2022 May 3;2(5):e0000316. doi: 10.1371/journal.pgph.0000316. eCollection 2022.
We previously described development of a rapid test for recent infection (RTRI) that can diagnose HIV infection and detect HIV-1 recent infections in a single device. This technology was transferred to a commercial partner as Asante Rapid Recency Assay (ARRA). We evaluated performance of the ARRA kits in the laboratory using a well-characterized panel of specimens. The plasma specimen panel (N = 1500) included HIV-1 (N = 570), HIV-2 (N = 10), and HIV-negatives (N = 920) representing multiple subtypes and geographic locations. Reference diagnostic data were generated using the Bio-Rad HIV-1-2-O EIA/Western blot algorithm with further serotyping performed using the Multispot HIV-1/2 assay. The LAg-Avidity EIA was used to generate reference data on recent and long-term infection for HIV-1 positive specimens at a normalized optical density (ODn) cutoff of 2.0 corresponding to a mean duration of about 6 months. All specimens were tested with ARRA according to the manufacturer's recommendations. Test strips were also read for line intensities using a reader and results were correlated with visual interpretation. ARRA's positive verification line (PVL) correctly classified 575 of 580 HIV-positive and 910 of 920 negative specimens resulting in a sensitivity of 99.1% (95% CI: 98.0-99.6) and specificity of 98.9% (95% CI: 98.1-99.4), respectively. The reader-based classification was similar for PVL with sensitivity of 99.3% (576/580) and specificity of 98.8% (909/920). ARRA's long-term line (LTL) classified 109 of 565 HIV-1 specimens as recent and 456 as long-term compared to 98 as recent and 467 as long-term (LT) by LAg-Avidity EIA (cutoff ODn = 2.0), suggesting a mean duration of recent infection (MDRI) close to 6 months. Agreement of ARRA with LAg recent cases was 81.6% (80/98) and LT cases was 93.8% (438/467), with an overall agreement of 91.7% (kappa = 0.72). The reader (cutoff 2.9) classified 109/566 specimens as recent infections compared to 99 by the LAg-Avidity EIA for recency agreement of 81.8% (81/99), LT agreement of 9% (439/467) with overall agreement of 91.9% (kappa = 0.72). The agreement between visual interpretation and strip reader was 99.9% (95% CI: 99.6-99.9) for the PVL and 98.1% (95% CI: 96.6-98.9) for the LTL. ARRA performed well with HIV diagnostic sensitivity >99% and specificity >98%. Its ability to identify recent infections is comparable to the LA-Avidity EIA corresponding to an MDRI of about 6 months. This point-of-care assay has implications for real-time surveillance of new infections among newly diagnosed individuals for targeted prevention and interrupting ongoing transmission thus accelerating epidemic control.
我们之前描述了一种近期感染快速检测方法(RTRI)的开发,该方法可在单一设备中诊断HIV感染并检测HIV-1近期感染情况。这项技术已转让给商业合作伙伴,成为阿桑特近期感染快速检测法(ARRA)。我们在实验室中使用一组特征明确的标本评估了ARRA试剂盒的性能。血浆标本组(N = 1500)包括HIV-1(N = 570)、HIV-2(N = 10)以及HIV阴性标本(N = 920),这些标本代表了多种亚型和地理位置。使用伯乐HIV-1-2-O酶免疫测定/免疫印迹算法生成参考诊断数据,并使用多重斑点HIV-1/2检测进行进一步的血清分型。LAg亲和力酶免疫测定用于为HIV-1阳性标本生成近期和长期感染的参考数据,标准化光密度(ODn)临界值为2.0,对应平均持续时间约为6个月。所有标本均按照制造商的建议用ARRA进行检测。还使用读数仪读取试纸条的条带强度,并将结果与目视判读结果进行关联。ARRA的阳性验证线(PVL)正确分类了580份HIV阳性标本中的575份以及920份阴性标本中的910份,灵敏度分别为99.1%(95%置信区间:98.0 - 99.6)和特异性为98.9%(95%置信区间:98.1 - 99.4)。基于读数仪的PVL分类情况类似,灵敏度为99.3%(576/580),特异性为98.8%(909/920)。与LAg亲和力酶免疫测定(临界值ODn = 2.0)相比,ARRA的长期线(LTL)将565份HIV-1标本中的109份分类为近期感染,456份分类为长期感染,而LAg亲和力酶免疫测定分别为98份近期感染和467份长期感染,这表明近期感染的平均持续时间(MDRI)接近6个月。ARRA与LAg近期感染病例的一致性为81.6%(80/98),与长期感染病例的一致性为93.8%(438/467),总体一致性为91.7%(kappa值 = 0.72)。读数仪(临界值2.9)将566份标本中的109份分类为近期感染,而LAg亲和力酶免疫测定为99份,近期感染一致性为81.8%(81/99),长期感染一致性为9%(439/467),总体一致性为91.9%(kappa值 = 0.72)。目视判读与试纸条读数仪之间对于PVL的一致性为99.9%(95%置信区间:99.6 - 99.9),对于LTL的一致性为98.1%(95%置信区间:96.6 - 98.9)。ARRA在HIV诊断方面表现良好,灵敏度>99%,特异性>98%。其识别近期感染的能力与对应MDRI约为6个月的LAg亲和力酶免疫测定相当。这种即时检测方法对于新诊断个体中新感染的实时监测具有重要意义,可用于针对性预防和阻断正在进行的传播,从而加速疫情控制。