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首页> 外文期刊>Journal of Clinical Microbiology >Radioimmunoassay for detection of antibodies to Epstein-Barr virus in human infectious mononucleosis serum specimens.
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Radioimmunoassay for detection of antibodies to Epstein-Barr virus in human infectious mononucleosis serum specimens.

机译:放射免疫分析法,用于检测人传染性单核细胞增多症血清标本中的爱泼斯坦-巴尔病毒抗体。

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摘要

A rapid microradioimmunoassay (RIA) technique was adapted for quantitatively measuring antibody titers to antigens occurring in Epstein-Barr virus (EBV)-infected lymphoid cells. In these experiments two EBV-infected cell lines, HR1K and EB-3, were used as antigen-positive cells and Molt-4 was used as the negative control cells. The antibody titers of sera from suspected infectious mononucleosis patients were compared by RIA and indirect fluorescent antibody (IFA) methods. As determined by each of the methods, 14 of 19 sera had positive antibody titers and the remainder of the sera had negative antibody titers. Thus, the two methods agreed completely in differentiating sera with antibodies to EBV antigens. To further evaluate the antibody specificity of the RIA, the antibody titers of paired sera, pre- or early infection and postinfection, from five confirmed infectious mononucleosis patients were determined by RIA and IFA. Seroconversion was demonstrated by both RIA and IFA for each of the patients. Thus, the sensitivity and specificity of the two procedures are about the same.
机译:快速微放射免疫分析(RIA)技术适用于定量测量针对爱泼斯坦-巴尔病毒(EBV)感染的淋巴样细胞中发生的抗原的抗体效价。在这些实验中,两种感染EBV的细胞系HR1K和EB-3被用作抗原阳性细胞,而Molt-4被用作阴性对照细胞。通过RIA和间接荧光抗体(IFA)方法比较了可疑传染性单核细胞增多症患者血清的抗体滴度。通过每种方法确定,19个血清中的14个具有阳性抗体滴度,其余血清具有阴性抗体滴度。因此,两种方法完全相同,可以用EBV抗原抗体区分血清。为了进一步评估RIA的抗体特异性,通过RIA和IFA确定了来自五名确诊的传染性单核细胞增多症患者的配对血清,配对感染或感染前或感染后的抗体滴度。 RIA和IFA均对每位患者进行了血清转化。因此,两种方法的敏感性和特异性大致相同。

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