Laboratory Branch, Division of HIV/AIDS Prevention, National Center for HIV/AIDS, Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
PLoS One. 2013 Oct 17;8(10):e77765. doi: 10.1371/journal.pone.0077765. eCollection 2013.
Accurate and reliable laboratory-based assays are needed for estimating HIV-1 incidence from cross-sectional samples. We recently described the development of a customized, HIV-1-specific Bio-Plex assay that allows for the measurement of HIV-specific antibody levels and avidity to multiple analytes for improved HIV-1 incidence estimates.
To assess intra- and inter-laboratory assay performance, prototype multiplex kits were developed and evaluated by three distinct laboratories. Longitudinal seroconversion specimens were tested in parallel by each laboratory and kit performance was compared to that of an in-house assay. Additionally, the ability of the kit to distinguish recent from long-term HIV-1 infection, as compared to the in-house assay, was determined by comparing the reactivity of known recent (infected <6 months) and long-term (infected >12 months) drug naïve specimens.
Although the range of reactivity for each analyte varied between the prototype kit and in-house assay, a measurable distinction in reactivity between recent and long-term specimens was observed with both assays in all three laboratories. Additionally, kit performance was consistent between all three laboratories. The intra-assay coefficient of variation (CV), between sample replicates for all laboratories, ranged from 0.5% to 6.1%. The inter-laboratory CVs ranged from 8.5% to 21.3% for gp160-avidity index (a) and gp120-normalized mean fluorescent intensity (MFI) value (n), respectively.
We demonstrate the feasibility of producing a multiplex kit for measuring HIV antibody levels and avidity, with the potential for improved incidence estimates based on multi-analyte algorithms. The availability of a commercial kit will facilitate the transfer of technology among diverse laboratories for widespread assay use.
需要准确可靠的实验室检测方法来估算来自横断面样本的 HIV-1 发病率。我们最近描述了一种定制的 HIV-1 特异性生物芯片检测方法的开发,该方法允许测量 HIV 特异性抗体水平和对多种分析物的亲和力,从而改善 HIV-1 发病率的估算。
为了评估实验室内部和实验室之间的检测性能,开发了原型多重试剂盒,并由三个不同的实验室进行评估。每个实验室均平行检测纵向血清转化样本,并将试剂盒的性能与内部检测进行比较。此外,通过比较已知近期(感染 <6 个月)和长期(感染 >12 个月)未经药物治疗的样本的反应性,来确定试剂盒与内部检测相比,区分近期和长期 HIV-1 感染的能力。
尽管每个分析物的反应性范围在原型试剂盒和内部检测之间有所不同,但在所有三个实验室中,这两种检测方法均观察到近期和长期样本之间的反应性存在可测量的差异。此外,试剂盒在所有三个实验室中的性能均一致。所有实验室的内样品重复性的变异系数(CV)在 0.5%至 6.1%之间。实验室间 CV 值分别为 gp160-亲和力指数(a)和 gp120-标准化平均荧光强度(MFI)值(n)的 8.5%至 21.3%。
我们证明了生产用于测量 HIV 抗体水平和亲和力的多重试剂盒的可行性,该试剂盒具有基于多分析物算法的改进发病率估算的潜力。商业试剂盒的出现将促进不同实验室之间的技术转移,以实现广泛的检测应用。