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Synthetic positive controls for ELISA test kits for detection of IgA and IgM antibodies to Chlamydia trachomatis

机译:ELISA检测试剂盒的合成阳性对照,用于检测IgA和IgM抗体对衣原体衣原体的抗体

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摘要

The enzyme-linked immunosorbent assay (ELISA) is the most informative and versatile method of serological diagnostics. The possibility of detecting by ELISA specific antibodies of different classes allow to differentiate primary infectious process and its remission, exacerbation and chronic disease (holding of differential diagnosis). This approach is implemented in the methodology for evaluation of patients for presence of humoral immune response against the causative agent of urogenital chlamydiosis. As with other infections immediately after Chlamydia trachomatis infection the specific IgM antibodies are formed, and subsequently basic projective antibodies of IgG class are synthesized. However, at exacerbation of chronic urogenital chlamydiosis specific IgA antibodies can be synthesized. That is why comprehensive evaluation of patients for presence of humoral immune response to Ch. trachomatis involves plasma testing of specific antibodies of all three classes. The essential problem in the production of ELISA diagnostic kits is obtaining of positive control. The classic version of positive control is human blood plasma containing specific antibodies. But specific IgM- and IgA-positive sera are deficit raw materials. This fact can significantly limit the production of diagnostic kits, especially in case of large-scale manufacture. We have suggested methodological approach to use of synthetic positive controls in indirect ELISA kits based on conjugate of normal human IgM (IgA) and monoclonal antibodies against major outer membrane protein of Ch. trachomatis. It was found that it’s possible to realize such task by means of NHS ester-maleimide-mediated conjugation (by sulfosuccinimidyl-4-(N-maleimidomethyl)cyclohexane-1-carboxylate) and reductive amination-mediated conjugation (by sodium periodate). It was found that synthetic positive controls obtained by different methods are characterized by higher titer compared to IgM- and IgA-positive high-titer serum. However, positive control obtained by NHS ester-mediated maleimide conjugation has the best titration profile characteristics, at the release time and after one-week storage at37 °C.
机译:酶联免疫吸附试验(ELISA)是血清学诊断最具信息性和多功能的方法。不同类别的ELISA特异性抗体检测的可能性允许区分原发性传染性过程及其缓解,恶化和慢性疾病(持有鉴别诊断)。这种方法是在评估患者对泌尿生殖器衣原体致病剂的体液免疫应答的情况下评估的方法中的方法。与衣原体衣原体感染后的其他感染一样,形成特异性IgM抗体,并合成IgG类的基本投射抗体。然而,在慢性泌尿介性衣原体的加剧时,可以合成特异性IgA抗体。这就是为什么综合评估患者对CH的体液免疫应答的存在。 Thachomatis涉及所有三类特异性抗体的血浆测试。 ELISA诊断试剂盒的生产中的基本问题是获得阳性对照。阳性对照的经典版本是含有特异性抗体的人血血浆。但特异性IgM-和IgA阳性血清是缺乏原料。这一事实可以显着限制诊断工具包的生产,特别是在大规模制造的情况下。我们已经建议使用基于正常人IgM(IgA)和单克隆抗体的间接ELISA试剂盒在间接ELISA试剂盒中使用合成阳性对照的方法方法方法,以及CH的主要外膜蛋白的缀合物。 Thachomatis。发现它可以通过NHS酯 - 马来酰亚胺介导的缀合(通过磺酰胺氨基甲基-4-(N-马来酰亚胺甲基)环己烷-1-羧酸酯)和还原胺化介导的缀合(通过钠碘酸钠)来实现这些任务。发现通过不同方法获得的合成阳性对照的特征在于与IGM和IGA阳性高滴度血清相比较高的滴度。然而,通过NHS酯介导的马来酰亚胺缀合获得的阳性对照具有最佳的滴定曲线特性,在释放时间和37℃的一周储存之后。

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