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采用雅培检测试剂盒酶免疫测定法检测鼻洗液中的呼吸道合胞病毒抗原。

Detection of respiratory syncytial virus antigen in nasal washings by Abbott TestPack enzyme immunoassay.

作者信息

Wren C G, Bate B J, Masters H B, Lauer B A

机构信息

University of Colorado School of Medicine, Denver 80262.

出版信息

J Clin Microbiol. 1990 Jun;28(6):1395-7. doi: 10.1128/jcm.28.6.1395-1397.1990.

Abstract

We compared the new Abbott TestPack (TP) respiratory syncytial virus (RSV) enzyme immunoassay (EIA) with cell culture and two commercial RSV EIAs (from Abbott Diagnostics and Kallestad Laboratories) by using split samples of fresh nasal washings from children with suspected RSV disease. Two tubes of HEp-2 cells were inoculated and observed for cytopathic effect for 14 days, and isolates were confirmed by immunofluorescence. The TP EIA was performed by following the manufacturer's instructions. Specimens positive by TP EIA but negative by culture were examined in a competitive inhibition (blocking) assay using the TP EIA, and rabbit anti-RSV serum. Of 218 specimens, 93 were positive by culture, 105 were positive by TP EIA, 80 were positive by the Abbott Diagnostics EIA, and 87 were positive by the Kallestad Laboratories EIA. The sensitivity, specificity, positive predictive value, and negative predictive value of the TP EIA were 92, 86, 81, and 93%, respectively. Of 20 apparently false-positive TP EIAs, 10 of 14 that were positive when retested were neutralized in the blocking assay, indicating that they were truly positive. The recalculated sensitivity, specificity, positive predictive value, and negative predictive value of the TP EIA were 92, 91, 90, and 93%, respectively. We conclude that the TP EIA is easy to perform, rapid (less than 0.5 h), and accurate.

摘要

我们使用疑似呼吸道合胞病毒(RSV)疾病患儿新鲜洗鼻液的分割样本,将新的雅培检测试剂盒(TP)呼吸道合胞病毒酶免疫测定法(EIA)与细胞培养法以及两种商用RSV EIA(来自雅培诊断公司和卡莱斯塔德实验室)进行了比较。接种两管HEp - 2细胞,并观察14天的细胞病变效应,分离株通过免疫荧光法进行确认。TP EIA按照制造商的说明进行操作。对TP EIA呈阳性但培养呈阴性的标本,使用TP EIA和兔抗RSV血清进行竞争抑制(阻断)试验检测。在218份标本中,93份培养呈阳性,105份TP EIA呈阳性,80份雅培诊断EIA呈阳性,87份卡莱斯塔德实验室EIA呈阳性。TP EIA的敏感性、特异性、阳性预测值和阴性预测值分别为92%、86%、81%和93%。在20份明显为TP EIA假阳性的标本中,重新检测时呈阳性的14份中有10份在阻断试验中被中和,表明它们是真正阳性。重新计算后,TP EIA的敏感性、特异性、阳性预测值和阴性预测值分别为92%、91%、90%和93%。我们得出结论,TP EIA操作简便、快速(少于0.5小时)且准确。

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