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Measurement of gp210 autoantibodies in sera of patients with primary biliary cirrhosis

机译:原发性胆汁性肝硬化患者血清中gp210自身抗体的测定

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摘要

Primary biliary cirrhosis (PBC) is an autoimmune liver disease with unknown etiology. Patients with PBC have antimitochondrial autoantibodies (AMA) and additionally 50% of them have antinuclear antibodies (ANA). A 15–amino acid fragment (DRKASPPSGLWSPAY) from the C‐terminal part of the nuclear envelope glycoprotein gp210 has been proposed as one of the antigenic targets for ANA. The aim of this work was to develop an immunoenzymatic assay for determination of gp210 autoantibodies using for its binding a synthetic pentadecapeptide derived from the gp210 amino acid sequence and to determine level of these autoantibodies in sera of patients with PBC and other autoimmune liver diseases from Poland. Polystyrene microtitration plates coated with the synthetic peptide were consecutively incubated with diluted sera, anti‐human immunoglobulin G (IgG) antibodies conjugated with horseradish peroxidase, and with tetramethylobenzidine. Optical density (OD) was read at 450 nm. The mean values of the intra‐ and interassay of variation coefficients of the test were 4.1 and 10.2%, respectively. Anti‐gp210 was detected in 44% of PBC patients and in 6% of patients with PSC. The results were negative for healthy blood donors and other controls. The specificity of the test was 99%, so the anti‐gp‐210 autoantibodies estimated on DRKASPPSGLWSPAY can be a reliable marker of PBC. J. Clin. Lab. Anal. 21:227–231, 2007. © 2007 Wiley‐Liss, Inc.
机译:原发性胆汁性肝硬化(PBC)是一种病因不明的自身免疫性肝病。 PBC患者具有抗线粒体自身抗体(AMA),此外,其中50%具有抗核抗体(ANA)。来自核被膜糖蛋白gp210 C末端的15个氨基酸的片段(DRKASPPSGLWSPAY)已被提议作为ANA的抗原靶标之一。这项工作的目的是开发一种用于测定gp210自身抗体的免疫酶分析法,该方法使用结合自gp210氨基酸序列的合成五肽来测定gp210自身抗体,并确定波兰PBC和其他自身免疫性肝病患者血清中这些自身抗体的水平。将涂有合成肽的聚苯乙烯微量滴定板与稀释的血清,与辣根过氧化物酶缀合的抗人免疫球蛋白G(IgG)抗体以及与四甲基联苯胺连续孵育。在450nm处读取光密度(OD)。检验内和批间变异系数的平均值分别为4.1和10.2%。在44%的PBC患者和6%的PSC患者中检测到抗gp210。对于健康的献血者和其他对照来说,结果是阴性的。该测试的特异性为99%,因此在DRKASPPSGLWSPAY上评估的抗gp-210自身抗体可以作为PBC的可靠标记。 J.临床实验室肛门21:227–231,2007。©2007 Wiley-Liss,Inc.

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