Hepojoki Satu, Rusanen Juuso, Hepojoki Jussi, Nurmi Visa, Vaheri Antti, Lundkvist Åke, Hedman Klaus, Vapalahti Olli
Medicum, Virology, University of Helsinki, Helsinki, Finland
Medicum, Virology, University of Helsinki, Helsinki, Finland.
J Clin Microbiol. 2015 Jul;53(7):2292-7. doi: 10.1128/JCM.00663-15. Epub 2015 May 13.
In this study, we describe a competitive homogeneous immunoassay that makes use of Förster resonance energy transfer (FRET) in rapid detection of pathogen-specific antibodies. The assay principle is based on competition between a monoclonal antibody (MAb) and serum antibodies to a given antigen. In the assay, named competitive FRET immunoassay (CFRET-IA), the FRET signal is induced if MAb carrying a donor label binds to an acceptor-labeled antigen. Specific antibodies in serum compete for antigen binding, resulting in reduced FRET signal. The proof-of-principle for the assay was obtained using donor-labeled Puumala virus nucleocapsid protein (PUUV-N) and acceptor-labeled anti-PUUV-N MAb. The assay was evaluated by analyzing 329 clinical samples comprising 101 from individuals with acute PUUV infection, 42 from individuals with past infection, and 186 from individuals with PUUV-seronegative sera, and the results were compared to those of reference tests. The rapid serodiagnostic test we introduced herein performed with 100% sensitivity and 99% specificity for diagnosing acute hantavirus disease.
在本研究中,我们描述了一种竞争性均相免疫测定法,该方法利用荧光共振能量转移(FRET)快速检测病原体特异性抗体。该测定原理基于单克隆抗体(MAb)与针对给定抗原的血清抗体之间的竞争。在名为竞争性FRET免疫测定法(CFRET-IA)的测定中,如果携带供体标记的MAb与受体标记的抗原结合,就会诱导产生FRET信号。血清中的特异性抗体竞争抗原结合,导致FRET信号减弱。使用供体标记的普马拉病毒核衣壳蛋白(PUUV-N)和受体标记的抗PUUV-N MAb获得了该测定法的原理验证。通过分析329份临床样本对该测定法进行评估,其中包括101份来自急性PUUV感染个体的样本、42份来自既往感染个体的样本以及186份来自PUUV血清阴性个体的样本,并将结果与参考测试结果进行比较。我们在此介绍的快速血清诊断测试在诊断急性汉坦病毒病时的灵敏度为100%,特异性为99%。