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Specificity of Antinuclear Autoantibodies Recognizing the Dense Fine Speckled Nuclear Pattern: Preferential Targeting of DFS70/LEDGFp75 Over its Interacting Partner MeCP2

机译:识别密集的有斑点的核模式的抗核自身抗体的特异性:DFS70 / LEDGFp75在其相互作用的伴侣MeCP2上的优先靶向

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摘要

Human antinuclear autoantibodies (ANAs) targeting the dense fine speckled (DFS) nuclear protein DFS70, commonly known as lens epithelium derived growth factor p75 (LEDGFp75), present a clinical puzzle since their significance remains elusive. While their frequencies are low in ANA-positive autoimmune rheumatic diseases, they are relatively elevated in clinical laboratory referrals, diverse inflammatory conditions, and ‘apparently’ healthy individuals. We reported previously that DFS70/LEDGFp75 is an autoantigen in prostate cancer that closely interacts with another 70 kD DFS nuclear protein, methyl CpG binding protein 2 (MeCP2). This led us to investigate if anti-DFS sera exclusively target DFS70/LEDGFp75 or also recognize MeCP2. Using several complementary autoantibody detection platforms and cellular/molecular approaches we evaluated 65 human sera producing anti-DFS autoantibodies. Our results show that these antibodies are highly specific for DFS70/LEDGFp75 and do not target MeCP2. Establishing the specificity of anti-DFS autoantibodies has implications for increasing our understanding their biological significance and clinical utility.
机译:靶向密集小斑点(DFS)核蛋白DFS70的人类抗核自身抗体(ANAs),通常被称为晶状体上皮衍生生长因子p75(LEDGFp75),由于其重要性仍然难以捉摸,因此在临床上引起了困惑。尽管它们在ANA阳性自身免疫性风湿性疾病中的发生率较低,但在临床实验室转诊,多种炎症情况和“显然”健康的个体中,它们的发生率相对较高。我们以前曾报道过DFS70 / LEDGFp75是前列腺癌中的一种自身抗原,它与另一个70 kD DFS核蛋白甲基CpG结合蛋白2(MeCP2)密切相互作用。这促使我们调查抗DFS血清是否仅靶向DFS70 / LEDGFp75或也识别MeCP2。使用几种互补的自身抗体检测平台和细胞/分子方法,我们评估了65种人血清产生的抗DFS自身抗体。我们的结果表明,这些抗体对DFS70 / LEDGFp75具有高度特异性,并且不靶向MeCP2。建立抗DFS自身抗体的特异性对提高我们对它们的生物学意义和临床实用性的了解具有重要意义。

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