Bellows Rae A, Rahn Kira L, Hummel Wyatt C, Mayton E Handly, Berry Henri W, Ryan Elizabeth P, Geiss Brian J, Dandy David S, Henry Charles S
Department of Chemistry, Colorado State University, Fort Collins, CO, 80523, USA.
Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, CO, 80523, USA.
Biosens Bioelectron. 2025 Nov 1;287:117640. doi: 10.1016/j.bios.2025.117640. Epub 2025 May 30.
Rapid and inexpensive quantification of antibody neutralizing efficiency is currently limited due to the use of live virus and strict biosafety level requirements necessary to perform a plaque reduction neutralization test (PRNT), severely restricting efficient evaluation of vaccine efficacy, establishment of correlates of protection, and determination of individual immune status for many viral diseases. Based on the surrogate virus neutralization test (sVNT), we demonstrate a magnetic bead-based electrochemical sVNT (esVNT) for sensitive quantification of SARS-CoV-2 antibody neutralization efficiency in under 15 min using a portable potentiostat. By utilizing magnetic beads as a solid phase for the capture probe and chronoamperometric detection, we show increased capture efficiency of reagents, minimal washing steps, and rapid signal generation without sacrificing sensitivity. The esVNT yields accurate quantification of neutralization efficiency for both monoclonal and polyclonal antibodies, even in the presence of potential interferents, as verified by comparison to sVNT. Spiked control serum and serum samples from a biorepository were evaluated, showing minimal matrix effects and the expected neutralization efficiency trends versus disease severity for esVNT compared to PRNT. Trends in PRNT and esVNT responses resulting from clonality, affinity, and neutralization mechanisms are also examined.
由于使用活病毒以及进行蚀斑减少中和试验(PRNT)所需的严格生物安全水平要求,目前快速且廉价地定量抗体中和效率受到限制,这严重制约了对许多病毒性疾病疫苗效力的有效评估、保护相关性的确立以及个体免疫状态的测定。基于替代病毒中和试验(sVNT),我们展示了一种基于磁珠的电化学sVNT(esVNT),可使用便携式恒电位仪在15分钟内灵敏地定量SARS-CoV-2抗体中和效率。通过利用磁珠作为捕获探针的固相并采用计时电流检测,我们展示了试剂捕获效率的提高、最少的洗涤步骤以及在不牺牲灵敏度的情况下快速产生信号。与sVNT相比,esVNT即使在存在潜在干扰物的情况下,也能对单克隆抗体和多克隆抗体的中和效率进行准确的定量。评估了来自生物样本库的加标对照血清和血清样本,结果显示与PRNT相比,esVNT的基质效应最小,且与疾病严重程度的中和效率趋势符合预期。还研究了由克隆性、亲和力和中和机制导致的PRNT和esVNT反应趋势。