Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA; NewYork-Presbyterian Hospital/Weill Cornell Medical Campus, New York, NY, USA.
ET HealthCare, Palo Alto, CA, USA.
Biosens Bioelectron. 2021 Apr 15;178:113008. doi: 10.1016/j.bios.2021.113008. Epub 2021 Jan 20.
The association of mortality with the early humoral response to SARS-CoV-2 infection within the first few days after onset of symptoms (DAOS) has not been thoroughly investigated partly due to a lack of sufficiently sensitive antibody testing methods. Here we report two sensitive and automated testing-on-a-probe (TOP) biosensor assays for SARS-CoV-2 viral specific total antibodies (TAb) and surrogate neutralizing antibodies (SNAb), which are suitable for clinical use. The TOP assays employ an RBD-coated quartz probe using a Cy5-Streptavidin-polysacharide conjugate to improve sensitivity and minimize interference. Disposable cartridges containing pre-dispensed reagents require no liquid manipulation or fluidics during testing. The TOP-TAb assay exhibited higher sensitivity in the 0-7 DAOS window than a widely used FDA-EUA assay. The rapid and automated TOP-SNAb correlated well with two well-established SARS-CoV-2 virus neutralization tests. The clinical utility of the TOP assays was demonstrated by evaluating early antibody responses in 120 SARS-CoV-2 RT-PCR positive adult hospitalized patients. Higher TAb and SNAb positivity rates and more robust antibody responses at patient's initial hospital presentation were seen in inpatients who survived COVID-19 than those who died in the hospital. Survival analysis using the Cox Proportional Hazards Model showed that patients who had negative TAb and/or SNAb at initial hospital presentation were at a higher risk of in-hospital mortality. Furthermore, TAb and SNAb levels at presentation were inversely associated with SARS-CoV-2 viral load based on concurrent RT-PCR testing. Overall, the sensitive and automated TAb and SNAb assays allow the detection of early SARS-CoV-2 antibodies which associate with mortality.
症状出现后几天内(DAOS)早期对 SARS-CoV-2 感染的体液反应与死亡率的相关性尚未得到彻底研究,部分原因是缺乏足够敏感的抗体检测方法。在这里,我们报告了两种灵敏且自动化的基于探针的检测(TOP)生物传感器测定法,用于检测 SARS-CoV-2 病毒特异性总抗体(TAb)和替代中和抗体(SNAb),这些方法适合临床应用。TOP 测定法使用包被 RBD 的石英探针,使用 Cy5-链霉亲和素-多糖缀合物来提高灵敏度并最小化干扰。含有预分配试剂的一次性试剂盒在测试过程中无需进行液体操作或流控。与广泛使用的 FDA-EUA 测定法相比,TOP-TAb 测定法在 0-7 DAOS 窗口中具有更高的灵敏度。快速且自动化的 TOP-SNAb 与两种成熟的 SARS-CoV-2 病毒中和测定法具有良好的相关性。通过评估 120 名 SARS-CoV-2 RT-PCR 阳性成年住院患者的早期抗体反应,证明了 TOP 测定法的临床实用性。在 COVID-19 住院患者中,与死亡患者相比,存活患者的 TAb 和 SNAb 阳性率更高,初始入院时的抗体反应更强。使用 Cox 比例风险模型进行的生存分析表明,在初始入院时 TAb 和/或 SNAb 阴性的患者在医院内死亡的风险更高。此外,根据同时进行的 RT-PCR 检测,入院时的 TAb 和 SNAb 水平与 SARS-CoV-2 病毒载量呈负相关。总的来说,灵敏且自动化的 TAb 和 SNAb 测定法可检测与死亡率相关的早期 SARS-CoV-2 抗体。