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时间分辨免疫荧光法:一种用于检测人血清中抗HIV抗体的灵敏且特异的检测方法。

Time-resolved immunofluorescence: a sensitive and specific assay for anti-HIV antibody detection in human sera.

作者信息

Aceti A, Titti F, Verani P, Buttò S, Pennica A, Sebastiani A, Rossi G B

机构信息

Department of Tropical and Infectious Diseases, La Sapienza University, Rome, Italy.

出版信息

J Virol Methods. 1987 Jul;16(4):303-15. doi: 10.1016/0166-0934(87)90015-2.

Abstract

We describe a new immunoassay, time-resolved fluoroimmunoassay (TR-FIA), for detection of anti-HIV antibodies in human sera. This method is based on the use of a crude virus preparation coated on a polystyrene microtitre plate and of a swine anti-human IgG labelled with a rare earth metal, europium, as fluorescent label chelated with EDTA derivatives. A light pulse from a xenon lamp (340 nm) was used to excite the label and after a 400 microseconds delay time the emission fluorescence was counted for 400 microseconds at 613 nm. This cycle was repeated 1000 times during the total counting time of 1 s. TR-FIA presents considerable advantages over other techniques: (a) it avoids time-consuming, expensive and hazardous virus purification steps; (b) it excludes the use of radiotracers or substrates with potential health risks to reveal the reaction; (c) it has high sensitivity and specificity. A total of 475 serum specimens were tested by ELISA and by TR-FIA. The proportions of positivity were 29.6% by ELISA versus 26.7% by TR-FIA. The sensitivity of both systems was 100%. The specificity was 87.5% for ELISA, whereas it reached a value of 99.4% for immunofluorimetric assay.

摘要

我们描述了一种用于检测人血清中抗HIV抗体的新型免疫测定法——时间分辨荧光免疫测定法(TR-FIA)。该方法基于将粗制病毒制剂包被在聚苯乙烯微量滴定板上,并使用用稀土金属铕标记的猪抗人IgG作为与EDTA衍生物螯合的荧光标记。用氙灯发出的光脉冲(340nm)激发标记物,在延迟400微秒后,于613nm处对发射荧光计数400微秒。在1秒的总计数时间内,此循环重复1000次。TR-FIA与其他技术相比具有显著优势:(a)它避免了耗时、昂贵且危险的病毒纯化步骤;(b)它无需使用对健康有潜在风险的放射性示踪剂或底物来揭示反应;(c)它具有高灵敏度和特异性。总共475份血清标本通过ELISA和TR-FIA进行检测。ELISA法的阳性比例为29.6%,而TR-FIA法为26.7%。两种系统的灵敏度均为100%。ELISA法的特异性为87.5%,而免疫荧光测定法的特异性达到99.4%。

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