Population Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia.
PLoS One. 2020 Dec 4;15(12):e0238010. doi: 10.1371/journal.pone.0238010. eCollection 2020.
Multiplexed bead-based assays that use Luminex® xMAP® technology have become popular for measuring antibodies against proteins of interest in many fields, including malaria and more recently SARS-CoV-2/COVID-19. There are currently two formats that are widely used: non-magnetic beads or magnetic beads. Data are lacking regarding the comparability of results obtained using these two types of beads, and for assays run on different instruments. Whilst non-magnetic beads can only be run on flow-based instruments (such as the Luminex® 100/200™ or Bio-Plex® 200), magnetic beads can be run on both these and the newer MAGPIX® instruments. In this study we utilized a panel of purified recombinant Plasmodium vivax proteins and samples from malaria-endemic areas to measure P. vivax-specific IgG responses using different combinations of beads and instruments. We directly compared: i) non-magnetic versus magnetic beads run on a Bio-Plex® 200, ii) magnetic beads run on the Bio-Plex® 200 versus MAGPIX® and iii) non-magnetic beads run on a Bio-Plex® 200 versus magnetic beads run on the MAGPIX®. We also performed an external comparison of our optimized assay. We observed that IgG antibody responses, measured against our panel of P. vivax proteins, were moderately-strongly correlated in all three of our comparisons (pearson r>0.5 for 18/19 proteins), however higher amounts of protein were required for coupling to magnetic beads. Our external comparison indicated that results generated in different laboratories using the same coupled beads are also highly comparable (pearson r>0.7), particularly if a reference standard curve is used.
基于微球的多重分析,使用 Luminex® xMAP® 技术,已在许多领域(包括疟疾和最近的 SARS-CoV-2/COVID-19)中成为测量针对感兴趣蛋白的抗体的流行方法。目前有两种广泛使用的格式:非磁性微球或磁性微球。关于使用这两种类型的微球以及在不同仪器上运行的分析获得的结果的可比性,数据仍然缺乏。虽然非磁性微球只能在基于流式的仪器(如 Luminex® 100/200™或 Bio-Plex® 200)上运行,但磁性微球可以在这些仪器和较新的 MAGPIX® 仪器上运行。在这项研究中,我们利用一组纯化的重组间日疟原虫蛋白和来自疟疾流行地区的样本,使用不同的微球和仪器组合来测量间日疟原虫特异性 IgG 反应。我们直接比较了:i)在 Bio-Plex® 200 上运行的非磁性与磁性微球,ii)在 Bio-Plex® 200 上运行的磁性微球与 MAGPIX®,以及 iii)在 Bio-Plex® 200 上运行的非磁性微球与在 MAGPIX®上运行的磁性微球。我们还对我们优化的分析进行了外部比较。我们观察到,针对我们的间日疟原虫蛋白面板测量的 IgG 抗体反应,在我们的所有三个比较中都呈中度到强相关性(18/19 个蛋白的皮尔逊 r>0.5),然而,磁性微球结合所需的蛋白量更高。我们的外部比较表明,使用相同偶联微球在不同实验室生成的结果也非常可比(皮尔逊 r>0.7),特别是如果使用参考标准曲线。