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商用免疫测定法在轮状病毒胃肠炎感染过程中用于诊断的比较效率

Comparative efficiency of commercial immunoassays for the diagnosis of rotavirus gastroenteritis during the course of infection.

作者信息

Miotti P G, Eiden J, Yolken R H

出版信息

J Clin Microbiol. 1985 Nov;22(5):693-8. doi: 10.1128/jcm.22.5.693-698.1985.

DOI:10.1128/jcm.22.5.693-698.1985
PMID:2997267
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC268507/
Abstract

We evaluated the performance characteristics of three commercially available immunoassays for the detection of rotavirus antigens in stool samples obtained from infants during the course of rotavirus gastroenteritis. Two of the assays, Bio-EnzaBead (Litton Bionetics, Charleston, S.C.) and Rotazyme (Abbott Laboratories, North Chicago, Ill.), are enzyme immunoassays, while the third, Rotalex (Medical Technology Corporation, Somerset, N.J.), is a latex agglutination assay. We tested a total of 122 samples obtained from 26 children with gastroenteritis; 56 samples, obtained from 21 children, were found to contain rotavirus antigen by a reference microplate enzyme immunoassay. Rotavirus antigen was found by the Bio-EnzaBead, Rotazyme, and Rotalex assays in 53, 42, and 29 samples, respectively. The true positivity of samples which were positive by the reference microplate assay but negative by the other assays was confirmed by a specific neutralization assay or by the visualization of bands of double-stranded RNA by polyacrylamide gel electrophoresis or both. No false-positive assay results were noted with any of the commercial assays. The sensitivity of the assays was determined to a great extent by the time after the onset of illness at which the specimen was collected. Thus, the sensitivity of commercial assays with specimens collected early in the course of illness did not differ significantly from that of the microplate assay. However, significantly lower degrees of sensitivity were noted later in the course of illness. Results of our studies indicate that all three commercial assays can accurately detect rotavirus in stools from children with rotavirus gastroenteritis. However, the choice of assay systems for use in the clinical laboratory will depend on the conditions in which stool specimens are collected and tested in the laboratory.

摘要

我们评估了三种市售免疫测定法在检测轮状病毒肠胃炎患儿粪便样本中轮状病毒抗原时的性能特征。其中两种测定法,即Bio-EnzaBead(Litton Bionetics公司,南卡罗来纳州查尔斯顿)和Rotazyme(雅培实验室,伊利诺伊州北芝加哥),是酶免疫测定法,而第三种Rotalex(医疗技术公司,新泽西州萨默塞特)是乳胶凝集测定法。我们总共检测了从26名肠胃炎患儿身上获取的122份样本;通过参考微孔板酶免疫测定法发现,从21名患儿身上获取的56份样本含有轮状病毒抗原。Bio-EnzaBead、Rotazyme和Rotalex测定法分别在53份、42份和29份样本中检测到轮状病毒抗原。通过参考微孔板测定法呈阳性但通过其他测定法呈阴性的样本的真阳性结果,通过特异性中和测定法或通过聚丙烯酰胺凝胶电泳观察双链RNA条带或两者同时进行确认。任何一种商业测定法均未出现假阳性检测结果。这些测定法的灵敏度在很大程度上取决于发病后采集标本的时间。因此,在疾病早期采集标本时,商业测定法的灵敏度与微孔板测定法相比无显著差异。然而,在疾病后期观察到灵敏度显著降低。我们的研究结果表明,所有三种商业测定法均可准确检测轮状病毒肠胃炎患儿粪便中的轮状病毒。然而,临床实验室中测定系统的选择将取决于实验室中粪便标本的采集和检测条件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1fd/268507/627f045bac55/jcm00112-0032-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1fd/268507/627f045bac55/jcm00112-0032-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1fd/268507/627f045bac55/jcm00112-0032-a.jpg

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