Department of Biosystems, Biosensors Group, KU Leuven, Willem de Croylaan 42, 3001 Leuven, Belgium.
PharmAbs, KU Leuven, Herestraat 49, Box 820, 3000 Leuven, Belgium.
ACS Sens. 2022 Feb 25;7(2):477-487. doi: 10.1021/acssensors.1c02215. Epub 2022 Jan 21.
The ongoing COVID-19 pandemic has emphasized the urgent need for rapid, accurate, and large-scale diagnostic tools. Next to this, the significance of serological tests (i.e., detection of SARS-CoV-2 antibodies) also became apparent for studying patients' immune status and past viral infection. In this work, we present a novel approach for not only measuring antibody levels but also profiling of binding kinetics of the complete polyclonal antibody response against the receptor binding domain (RBD) of SARS-CoV-2 spike protein, an aspect not possible to achieve with traditional serological tests. This fiber optic surface plasmon resonance (FO-SPR)-based label-free method was successfully accomplished in COVID-19 patient serum and, for the first time, directly in undiluted whole blood, omitting the need for any sample preparation. Notably, this bioassay (1) was on par with FO-SPR sandwich bioassays (traditionally regarded as more sensitive) in distinguishing COVID-19 from control samples, irrespective of the type of sample matrix, and (2) had a significantly shorter time-to-result of only 30 min compared to >1 or 4 h for the FO-SPR sandwich bioassay and the conventional ELISA, respectively. Finally, the label-free approach revealed that no direct correlation was present between antibody levels and their kinetic profiling in different COVID-19 patients, as another evidence to support previous hypothesis that antibody-binding kinetics against the antigen in patient blood might play a role in the COVID-19 severity. Taking all this into account, the presented work positions the FO-SPR technology at the forefront of other COVID-19 serological tests, with a huge potential toward other applications in need for quantification and kinetic profiling of antibodies.
持续的 COVID-19 大流行强调了快速、准确和大规模诊断工具的迫切需求。除此之外,血清学检测(即检测 SARS-CoV-2 抗体)的重要性也在研究患者的免疫状态和过去的病毒感染方面变得明显。在这项工作中,我们提出了一种新的方法,不仅可以测量抗体水平,还可以分析针对 SARS-CoV-2 刺突蛋白受体结合域(RBD)的完整多克隆抗体反应的结合动力学特征,这是传统血清学检测无法实现的。这种基于光纤表面等离子体共振(FO-SPR)的无标记方法在 COVID-19 患者血清中成功实现,并且首次直接在未经稀释的全血中实现,无需任何样品制备。值得注意的是,该生物测定法(1)在区分 COVID-19 与对照样本方面与 FO-SPR 夹心生物测定法(传统上被认为更灵敏)相当,无论样本基质类型如何,(2)与 FO-SPR 夹心生物测定法和传统 ELISA 相比,结果的获得时间显著缩短,仅为 30 分钟,而分别为>1 或 4 小时。最后,无标记方法表明,不同 COVID-19 患者的抗体水平与其动力学特征之间没有直接相关性,这进一步支持了先前的假设,即患者血液中针对抗原的抗体结合动力学可能在 COVID-19 严重程度中起作用。考虑到所有这些,所提出的工作使 FO-SPR 技术处于其他 COVID-19 血清学检测的前沿,具有在需要定量和动力学分析抗体的其他应用中巨大的潜力。