...
首页> 外文期刊>Journal of Clinical Microbiology >Rapid Homogeneous Immunoassay Based on Time-Resolved F?rster Resonance Energy Transfer for Serodiagnosis of Acute Hantavirus Infection
【24h】

Rapid Homogeneous Immunoassay Based on Time-Resolved F?rster Resonance Energy Transfer for Serodiagnosis of Acute Hantavirus Infection

机译:基于时间分辨弗氏共振能量转移的快速同质免疫测定用于急性汉坦病毒感染的血清学诊断。

获取原文
           

摘要

We recently introduced a homogeneous immunoassay based on time-resolved F?rster 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.
机译:我们最近介绍了一种基于时间分辨的Fsterster共振能量转移(TR-FRET)的均相免疫测定法,该时间分辨是由荧光团标记的抗原和荧光团标记的蛋白L(与免疫球蛋白结合)引起的。作为第一个临床应用,我们将这种方法(LFRET)用于Puumala汉坦病毒(PUUV)感染的血清诊断。包含来自急性( n = 21)或过去( n = 17)PUUV感染者血清和PUUV血清阴性个体( n = < / em> 20)来定义参数。使用前瞻性采集的血清样本(面板2; n = 153)评估了临床检测的性能。根据面板1的结果,将阳性阈值设置为比背景高3倍的信号水平,而将信号比背景水平低3倍的信号水平视为PUUV血清阴性。在第1组中,与0/20血清阴性药物相比,有20/21急性感染和7/10过去感染样品诱导出阳性信号。在第2组中,与7/103血清阴性药相比,在39/40急性感染和4/10既往感染样品中获得了阳性信号。但是,在IgG耗尽后,58/61急性感染样品为LFRET阳性,而所有过去感染和血清阴性样品均为阴性,相当于检测急性PUUV感染的100%特异性和95%灵敏度。我们证明了这种新型的免疫分析方法是一种快速的血清学诊断急性肺炎性肺炎病毒感染的有前途的工具。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号