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使用两种酶联免疫吸附测定法对巨细胞病毒特异性抗体进行定量和定性检测。

Quantitative and qualitative detection of cytomegalovirus-specific antibodies using two types of enzyme-linked immunosorbent assay.

作者信息

Kinane K A, Hillary I B

出版信息

J Med Virol. 1985 Aug;16(4):375-84. doi: 10.1002/jmv.1890160411.

DOI:10.1002/jmv.1890160411
PMID:2993506
Abstract

An indirect ELISA and an inhibition ELISA were developed for the detection of cytomegalovirus (CMV)-specific immunoglobulin G (IgG) and CMV-specific total immunoglobulin, respectively. Both assays were more specific than the complement fixation (CF) test, and titres of positive sera were 660 times higher by IgG ELISA and 6 times higher by inhibition ELISA than titres by the CF test. Titres by IgG ELISA were reliably determined using the absorbance obtained at a single serum dilution of 1/1,000 in conjunction with a standard graph. Both ELISAs compared favourably with each other in sensitivity and specificity in determining CMV immune status. The inhibition ELISA, in particular, provides a simple and reliable method of screening sera, which requires no control antigen or predilution of sera. It should prove useful for large-scale screening procedures, such as blood donor testing.

摘要

分别开发了一种间接酶联免疫吸附测定法(ELISA)和一种抑制酶联免疫吸附测定法,用于检测巨细胞病毒(CMV)特异性免疫球蛋白G(IgG)和CMV特异性总免疫球蛋白。这两种测定法均比补体结合(CF)试验更具特异性,IgG ELISA检测阳性血清的效价比CF试验高660倍,抑制ELISA检测阳性血清的效价比CF试验高6倍。通过在1/1000单一血清稀释度下获得的吸光度结合标准曲线,可可靠地测定IgG ELISA的效价。在确定CMV免疫状态方面,两种ELISA在敏感性和特异性上相互比较效果良好。特别是抑制ELISA提供了一种简单可靠的血清筛查方法,无需对照抗原或血清预稀释。它对于大规模筛查程序,如献血者检测,应是有用的。

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