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A new luminescence assay for autoantibodies to mammalian cell-prepared insulinoma-associated protein 2

机译:一种新的发光检测方法,用于哺乳动物细胞制备的胰岛素瘤相关蛋白2的自身抗体

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摘要

OBJECTIVE - Insulinoma-associated protein 2 (IA-2) is a major autoantigen in type I diabetes, and IA-2 autoantibodies are routinely detected by a liquid-phase radioimmunoprecipitation assay. The present experiments were initiated to develop a new assay that does not require the use of radioisotopes or autoantigens prepared in bacteria or by in vitro transcription/translation. RESEARCH DESIGN AND METHODS - IA-2 luciferase fusion protein was expressed in mammalian cells and assayed for autoantibodies by liquid-phase luciferase immunoprecipitation. RESULTS - Our study showed that there was no significant difference between the luciferase immunoprecipitation and the radioimmunoprecipitation assays in sensitivity and specificity, and comparison of the two assays revealed a high correlation coefficient (R-2 = 0.805). CONCLUSIONS - The luciferase system offers a robust, inexpensive, nonradioactive method for the detection of autoantibodies to mammalian cell-prepared IA-2 and could be of practical value at the clinical level.
机译:目的-胰岛素瘤相关蛋白2(IA-2)是I型糖尿病的主要自身抗原,IA-2自身抗体通常通过液相放射免疫沉淀测定法进行检测。开始本实验以开发不需要使用在细菌中或通过体外转录/翻译制备的放射性同位素或自身抗原的新测定法。研究设计与方法-IA-2荧光素酶融合蛋白在哺乳动物细胞中表达,并通过液相荧光素酶免疫沉淀法测定自身抗体。结果-我们的研究表明,萤光素酶免疫沉淀法和放射免疫沉淀法在敏感性和特异性上没有显着差异,并且两种方法的比较显示出很高的相关系数(R-2 = 0.805)。结论-萤光素酶系统为检测针对哺乳动物细胞制备的IA-2的自身抗体提供了一种可靠,廉价,非放射性的方法,在临床上具有实用价值。

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