Huang Rui-Lin, Fu Yi-Chen, Wang Yung-Chih, Hong Chitsung, Yang Wei-Chieh, Wang I-Jen, Sun Jun-Ren, Chen Yunching, Shen Ching-Fen, Cheng Chao-Min
Institute of Biomedical Engineering, National Tsing Hua University, Hsinchu 30013, Taiwan.
National Defense Medical Center, Department of Internal Medicine, Division of Internal Medicine and Tropical Medicine, Tri-Service General Hospital, Taipei 11490, Taiwan.
Vaccines (Basel). 2022 Feb 10;10(2):271. doi: 10.3390/vaccines10020271.
As of August 2021, there have been over 200 million confirmed case of coronavirus disease 2019 caused by severe acute respiratory syndrome coronavirus and more than 4 million COVID-19-related deaths globally. Although real-time polymerase chain reaction is considered to be the primary method of detection for SARS-CoV-2 infection, the use of serological assays for detecting COVID-19 antibodies has been shown to be effective in aiding with diagnosis, particularly in patients who have recovered from the disease and those in later stages of infection. Since it has a high detection rate and few limitations compared to conventional enzyme-linked immunosorbent assay protocols, we used a lateral flow immunoassay as our diagnostic tool of choice. Since lateral flow immunoassay results interpreted by the naked eye may lead to erroneous diagnoses, we developed an innovative, portable device with the capacity to capture a high-resolution reflectance spectrum as a means of promoting diagnostic accuracy. We combined this spectrum-based device with commercial lateral flow immunoassays to detect the neutralizing antibody in serum samples collected from 30 COVID-19-infected patients (26 mild cases and four severe cases). The results of our approach, lateral flow immunoassays coupled with a spectrum-based reader, demonstrated a 0.989 area under the ROC curve, 100% sensitivity, 95.7% positive predictive value, 87.5% specificity, and 100% negative predictive value. As a result, our approach exhibited great value for neutralizing antibody detection. In addition to the above tests, we also tested plasma samples from 16 AstraZeneca-vaccinated (ChAdOx1nCoV-19) patients and compared our approach and enzyme-linked immunosorbent assay results to see whether our approach could be applied to vaccinated patients. The results showed a high correlation between these two approaches, indicating that the lateral flow immunoassay coupled with a spectrum-based reader is a feasible approach for diagnosing the presence of a neutralizing antibody in both COVID-19-infected and vaccinated patients.
截至2021年8月,由严重急性呼吸综合征冠状病毒2引起的2019冠状病毒病确诊病例已超过2亿例,全球与新冠病毒相关的死亡人数超过400万。尽管实时聚合酶链反应被认为是检测严重急性呼吸综合征冠状病毒2感染的主要方法,但血清学检测用于检测新冠病毒抗体已被证明在辅助诊断方面有效,特别是对于已从疾病中康复的患者以及处于感染后期的患者。由于与传统酶联免疫吸附测定方案相比,它具有高检测率和较少的局限性,我们选择使用侧向流动免疫测定作为我们的诊断工具。由于肉眼解读的侧向流动免疫测定结果可能导致错误诊断,我们开发了一种创新的便携式设备,该设备能够捕获高分辨率反射光谱,以此提高诊断准确性。我们将这种基于光谱的设备与商业侧向流动免疫测定相结合,以检测从30名新冠病毒感染患者(26例轻症和4例重症)采集的血清样本中的中和抗体。我们的方法,即侧向流动免疫测定与基于光谱的读数器相结合,结果显示受试者工作特征曲线下面积为0.989,灵敏度为100%,阳性预测值为95.7%,特异性为87.5%,阴性预测值为100%。因此,我们的方法在中和抗体检测方面显示出巨大价值。除上述测试外,我们还检测了16名接种阿斯利康疫苗(ChAdOx1 nCoV-19)患者的血浆样本,并比较了我们的方法和酶联免疫吸附测定结果,以查看我们的方法是否可应用于接种疫苗的患者。结果表明这两种方法之间具有高度相关性,表明侧向流动免疫测定与基于光谱的读数器相结合是诊断新冠病毒感染患者和接种疫苗患者中中和抗体存在情况的可行方法。