原发性胆汁性肝硬化中M2抗体酶抑制作用的自动微量测定。

K L Teoh, M J Rowley, I R Mackay
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引用次数: 17

摘要

在原发性胆汁性肝硬化(PBC)中,产生针对线粒体抗原M2组的自身抗体,其中主要成分是丙酮酸脱氢酶复合物(PDC)的E2亚基。根据分光光度法的宏观抑制试验,这些抗体除了与PDC的常规反应性外,还在体外抑制PDC的催化功能。我们描述了一种微抑制试验,适用于微滴板和ELISA板阅读器自动读出结果。我们表明,这种微量测定法具有类似于大测定法的灵敏度。在一项对83份PBC和其他疾病的血清进行的研究中,抑制微测定证明对PBC有特异性。这种对PBC血清的自动抑制微测定可能成为诊断PBC的主要实验室程序,特别是因为它可以识别PBC- e2上实际自身表位的抗体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An automated microassay for enzyme inhibitory effects of M2 antibodies in primary biliary cirrhosis.

In primary biliary cirrhosis (PBC), autoantibodies are produced to the M2 group of mitochondrial antigens, of which a major constituent is the E2 subunit of the pyruvate dehydrogenase complex (PDC). These antibodies, in addition to conventional reactivities with PDC, characteristically inhibit the catalytic function of PDC in vitro, as judged by a macroinhibition assay based on spectrophotometry. We describe a microinhibition assay adapted for microtitre plates and for an automated readout of results by an ELISA plate reader. We show that this microassay has a sensitivity similar to that of the macroassay. In a study of 83 sera, from PBC and other diseases, the inhibitory microassay proved specific for PBC. This automated inhibitory microassay for PBC-sera could become a primary laboratory procedure for the diagnosis of PBC, particularly because it may identify antibodies to the actual autoepitope on the PDC-E2.

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