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基于时间分辨荧光共振能量转移的快速均相免疫分析用于急性汉坦病毒感染的血清学诊断

Rapid homogeneous immunoassay based on time-resolved Förster resonance energy transfer for serodiagnosis of acute hantavirus infection.

作者信息

Hepojoki Satu, Hepojoki Jussi, Hedman Klaus, Vapalahti Olli, Vaheri Antti

机构信息

Department of Virology, University of Helsinki, Helsinki, Finland.

Department of Virology, University of Helsinki, Helsinki, Finland

出版信息

J Clin Microbiol. 2015 Feb;53(2):636-40. doi: 10.1128/JCM.02994-14. Epub 2014 Dec 17.

Abstract

We recently introduced a homogeneous immunoassay based on time-resolved Förster resonance energy transfer (TR-FRET) elicited by fluorophore-labeled antigen and fluorophore-labeled protein L, bound by an immunoglobulin. As the first clinical application, we employ this approach (LFRET) in serodiagnosis of Puumala hantavirus (PUUV) infection. A reference panel containing serum from individuals with acute (n = 21) or past (n = 17) PUUV infection and from PUUV-seronegative individuals (n = 20) was used to define the parameters. The clinical assay performance was evaluated with a prospectively collected serum panel (panel 2; n = 153). Based on the results for panel 1, the threshold for positivity was set at a signal level that was 3-fold over background, while those with a signal <3-fold over the background level were considered PUUV seronegative. With panel 1, 20/21 acute- and 7/10 past-infection samples induced positive signals, compared to 0/20 seronegatives. With panel 2, a positive signal was obtained in 39/40 acute- and 4/10 past-infection samples, as opposed to 7/103 seronegatives. However, after IgG depletion, 58/61 acute-infection samples were LFRET positive, while all past-infection and seronegative samples were negative, corresponding to 100% specificity and 95% sensitivity in detection of acute PUUV infection. We demonstrate that the novel immunoassay is a promising tool for rapid serodiagnosis of acute Puumala virus infection.

摘要

我们最近推出了一种基于时间分辨荧光共振能量转移(TR-FRET)的均相免疫测定法,该方法由荧光团标记的抗原和荧光团标记的蛋白L引发,二者由免疫球蛋白结合。作为首个临床应用,我们将这种方法(LFRET)用于普马拉汉坦病毒(PUUV)感染的血清学诊断。使用一个参考样本组来确定参数,该样本组包含急性(n = 21)或既往(n = 17)PUUV感染个体以及PUUV血清阴性个体(n = 20)的血清。用前瞻性收集的血清样本组(样本组2;n = 153)评估临床检测性能。根据样本组1的结果,阳性阈值设定为比背景信号高3倍的信号水平,而信号<背景水平3倍的样本被视为PUUV血清阴性。对于样本组1,20/21例急性感染样本和7/10例既往感染样本诱导出阳性信号,而20例血清阴性样本均为阴性。对于样本组2,39/40例急性感染样本和4/10例既往感染样本获得阳性信号,而103例血清阴性样本中有7例为阳性。然而,在去除IgG后,58/61例急性感染样本LFRET呈阳性,而所有既往感染和血清阴性样本均为阴性,在检测急性PUUV感染时特异性为100%,敏感性为95%。我们证明,这种新型免疫测定法是快速血清学诊断急性普马拉病毒感染的一种有前景的工具。

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