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用于检测正痘病毒抗体的酶联免疫吸附测定(ELISA)标准化

Standardization of ELISA for detection of antibodies to orthopoxviruses.

作者信息

Maltseva N N, Marennikova S S, Matsevich G R, Stepanova L G, Habahpasheva N A

出版信息

Acta Virol. 1985 Jul;29(4):294-8.

PMID:2864832
Abstract

The experience with ELISA technique utilized at serological screening for orthopoxviruses in the Republic of Ivory Coast revealed factors reducing the sensitivity and the specificity of the test. It was found out that routine controls such as "positive" and "negative" sera as well as the accepted reading of the results by two-fold or higher increase of OD values as compared to the "negative" control may be not sufficient. A significantly enhanced sensitivity and specificity of reaction was achieved by simultaneous examination of each serum under study with a control antigen. Selection of optimal dilutions of each test component followed by spectrophotometric assay and calculation of results according to the given formula contributed to the same aim. As a result of these improvements the rate of antibody detection among revaccinees was enhanced from 19 to 78.8% and the titres of ELISA and virus neutralization tests correlated in 88% of cases.

摘要

在科特迪瓦共和国使用酶联免疫吸附测定(ELISA)技术进行正痘病毒血清学筛查的经验揭示了降低该检测灵敏度和特异性的因素。结果发现,常规对照如“阳性”和“阴性”血清,以及与“阴性”对照相比,以OD值两倍或更高增幅作为结果的公认判读方式可能并不充分。通过用对照抗原同时检测每份待测血清,反应的灵敏度和特异性得到显著提高。选择每种检测成分的最佳稀释度,随后进行分光光度测定并根据给定公式计算结果,也有助于实现这一目标。这些改进的结果是,再接种者中的抗体检测率从19%提高到78.8%,并且在88%的病例中,ELISA和病毒中和试验的滴度具有相关性。

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