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用于检测 COVID-19 患者血清和全血中抗 RBD 抗体的创新 FO-SPR 无标记策略。

Innovative FO-SPR Label-free Strategy for Detecting Anti-RBD Antibodies in COVID-19 Patient Serum and Whole Blood.

机构信息

Department of Biosystems, Biosensors Group, KU Leuven, Willem de Croylaan 42, 3001 Leuven, Belgium.

PharmAbs, KU Leuven, Herestraat 49, Box 820, 3000 Leuven, Belgium.

出版信息

ACS Sens. 2022 Feb 25;7(2):477-487. doi: 10.1021/acssensors.1c02215. Epub 2022 Jan 21.

Abstract

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.

摘要

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。

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