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用于检测沙眼衣原体热休克蛋白(HSP - 60)特异性IgG抗体的酶联免疫吸附测定的特点。

Characteristics of enzyme-linked immunosorbent assay for detection of IgG antibodies specific to Сhlamydia trachomatis heat shock protein (HSP-60).

作者信息

Galkin O Yu, Besarab A B, Lutsenko T N

出版信息

Ukr Biochem J. 2017 Jan-Feb;89(1):22-30. doi: 10.15407/ubj89.01.022.

DOI:10.15407/ubj89.01.022
PMID:29236386
Abstract

The goal of this work was to study sensitivity and specificity of the developed ELISA set for the identification of IgG antibodies against Chlamydia trachomatis HSP-60 (using biotinylated tyramine-based signal amplification system). The study was conducted using a panel of characterized sera, as well as two reference ELISA sets of similar purpose. According to the results of ELISA informative value parameters, the ELISA we have developed showed the highest specificity and sensitivity parameters (no false negative or false positive results were registered). In 4 out of 15 intralaboratory panel serum samples initially identified as negative, anti-HSP-60 IgG-antibodies test result in reference ELISA sets upon dilution changed from negative to positive. The nature of titration curves of false negative sera and commercial monoclonal antibodies А57-В9 against C. trachomatis HSP-60 after incubation for 24 h was indicative of the presence of anti-idiotypic antibodies in these samples. Upon sera dilution, idiotypic-anti-idiotypic complexes dissociated, which caused the change of test result. High informative value of the developed ELISA set for identification of IgG antibodies against C. trachomatis HSP-60 has been proven. Anti-idiotypic antibodies possessing C. trachomatis anti-HSP-60 activity and being one of the causes of false negative results of the relevant ELISA-based tests have been identified in blood sera of individuals infected with chlamydial genitourinary infection agents.

摘要

这项工作的目标是研究已开发的酶联免疫吸附测定(ELISA)试剂盒用于鉴定抗沙眼衣原体热休克蛋白60(HSP-60)IgG抗体的敏感性和特异性(使用基于生物素化酪胺的信号放大系统)。该研究使用了一组经过特征鉴定的血清以及两个类似用途的参考ELISA试剂盒进行。根据ELISA信息价值参数的结果,我们开发的ELISA显示出最高的特异性和敏感性参数(未记录到假阴性或假阳性结果)。在最初鉴定为阴性的15个实验室内部血清样本中,有4个样本在参考ELISA试剂盒中经稀释后抗HSP-60 IgG抗体检测结果从阴性变为阳性。假阴性血清和针对沙眼衣原体HSP-60的商业单克隆抗体A57-B9孵育24小时后的滴定曲线性质表明这些样本中存在抗独特型抗体。血清稀释后,独特型-抗独特型复合物解离,导致检测结果改变。已证明所开发的ELISA试剂盒对于鉴定抗沙眼衣原体HSP-60 IgG抗体具有很高的信息价值。在感染衣原体性泌尿生殖感染病原体的个体血清中已鉴定出具有沙眼衣原体抗HSP-60活性且是相关ELISA检测假阴性结果原因之一的抗独特型抗体。

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