Nelson Julie A E, Hawkins J Tyler, Schanz Maria, Mollan Katie, Miller Melissa B, Schmitz John L, Fiscus Susan A
UNC Center for AIDS Research, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA; Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
UNC Center for AIDS Research, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA; Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
J Clin Virol. 2014 Aug;60(4):418-21. doi: 10.1016/j.jcv.2014.05.012. Epub 2014 Jun 2.
The current gold standard for infant diagnosis of HIV-1 is the Roche Amplicor Qualitative DNA assay, but it is being phased out.
Compare the Abbott qualitative assay and the Gen-Probe Aptima assay to the gold standard Roche DNA assay using dried blood spots (DBS).
The Gen-Probe Aptima and Abbott qualitative HIV-1 assays were compared to the Roche DNA assay for early infant diagnosis. Specificity and sensitivity were determined for the three assays using DBS from 50 HIV-exposed uninfected infants and 269 HIV-1 infected adults from North Carolina, respectively. All of the negative and 151 of the positive DBS had valid results on the 3 different assays, and an additional 118 positive DBS had valid results on the Roche DNA and Aptima assays.
All three assays were very specific. The Roche DNA assay was the most sensitive (96.7%) over a wide range of HIV PVL, including samples with PVL<400 copies/ml. Restricted to samples with PVL>400 copies/ml, the Gen-Probe Aptima assay had sensitivity (96.5%) comparable to the Roche DNA assay (98.8%). The Abbott Qualitative assay was the least sensitive and only had sensitivity above 95% among samples with PVL over 1000 copies/ml.
The Abbott HIV-1 Qualitative assay was not as sensitive as the comparator assays, so it would not be a useful replacement assay, especially for infants taking antiretroviral prophylaxis. The Gen-Probe Aptima assay is an adequate replacement option for infant diagnosis using DBS.
目前用于婴儿HIV-1诊断的金标准是罗氏Amplicor定性DNA检测法,但该方法正在逐步淘汰。
使用干血斑(DBS)将雅培定性检测法和Gen-Probe Aptima检测法与金标准罗氏DNA检测法进行比较。
将Gen-Probe Aptima和雅培HIV-1定性检测法与罗氏DNA检测法进行比较,用于早期婴儿诊断。分别使用来自北卡罗来纳州50名暴露于HIV但未感染的婴儿和269名HIV-1感染成人的DBS来确定这三种检测方法的特异性和敏感性。所有阴性和151份阳性DBS在3种不同检测方法上均有有效结果,另外118份阳性DBS在罗氏DNA检测法和Aptima检测法上有有效结果。
所有三种检测方法都具有很高的特异性。罗氏DNA检测法在广泛的HIV病毒载量范围内最为敏感(96.7%), 包括病毒载量<400拷贝/ml的样本。对于病毒载量>400拷贝/ml的样本,Gen-Probe Aptima检测法的敏感性(96.5%)与罗氏DNA检测法(98.8%)相当。雅培定性检测法最不敏感,仅在病毒载量超过1000拷贝/ml的样本中敏感性高于95%。
雅培HIV-1定性检测法不如对照检测法敏感,因此它不是一种有用的替代检测法,特别是对于接受抗逆转录病毒预防治疗的婴儿。Gen-Probe Aptima检测法是使用DBS进行婴儿诊断的一种合适的替代选择。