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首页> 外文期刊>Journal of cutaneous pathology >A predominant IgG4 subclass may be responsible for false-negative direct immunofluorescence in bullous pemphigoid.
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A predominant IgG4 subclass may be responsible for false-negative direct immunofluorescence in bullous pemphigoid.

机译:主要的IgG4亚类可能是大疱性类天疱疮的假阴性直接免疫荧光。

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摘要

BACKGROUND: Bullous pemphigoid (BP) is an immune-mediated blistering disease, usually characterized immunopathologically by the linear deposition of IgG and C3 along the basement membrane zone (BMZ) of skin. However, positive deposition of C3 but negative staining for IgG on direct immunofluorescence (DIF) studies has been noted in some patients. METHODS: Twelve patients known to have BP but with absence of staining for IgG were included in this study. Frozen sections of skin specimens from the 12 patients were subjected to IgG DIF, as well as a sandwich double antibody method of staining for IgG, IgG subclasses, and light chains. Enzyme-linked immunosorbent assay (ELISA) using commercially available human IgG subclasses was used to analyze the subclass restriction of FITC-labeled antihuman IgG conjugates. RESULTS: Of the 12 skin specimens with positive C3 and negative IgG on DIF, nine were positive for IgG with the double antibody sandwich method. In addition, all 12 specimens had positive linear staining for the subclass IgG4 along the BMZ with this method. There was no IgG light chain restriction. Two commercially obtained antihuman IgG conjugates, both commonly used in our laboratory for DIF testing, were analyzed for separate IgG subclass specificity by ELISA. Both conjugates showed high reactivity to IgG1 and IgG3 with less reactivity to IgG2 and IgG4. CONCLUSION: These results suggest that the following factors contribute to false-negative staining for IgG on DIF in some BP patients: (i): subthreshold IgG in skin specimens; (ii) limited reactivity of commercial antihuman IgG conjugates to the IgG4 subclass; and (iii) decreased sensitivity of DIF compared with double antibody methods for the detection of IgG. The use of sandwich double antibody immunofluorescence methods to test for IgG and/or IgG subclasses may be helpful in definitively diagnosing BP in patients with negative IgG and positive C3 staining on DIF.
机译:背景:大疱性类天疱疮(BP)是一种免疫介导的水疱性疾病,通常在免疫病理学上以IgG和C3沿皮肤基底膜区(BMZ)线性沉积为特征。但是,在某些患者中,已经注意到在直接免疫荧光(DIF)研究中C3阳性沉积,但IgG阴性。方法:本研究包括十二名已知患有BP但无IgG染色的患者。对来自12位患者的皮肤标本的冷冻切片进行IgG DIF以及IgG,IgG亚类和轻链染色的夹心双抗体法。使用可商购的人IgG亚类进行的酶联免疫吸附测定(ELISA)用于分析FITC标记的抗人IgG缀合物的亚类限制性。结果:在DIF上C3阳性和IgG阴性的12个皮肤样本中,双抗体夹心法中有9个IgG阳性。此外,使用该方法,所有12个样本的BMZ沿亚类IgG4均呈阳性线性染色。没有IgG轻链限制。通过ELISA分析了两种通常在我们实验室中用于DIF测试的商业获得的抗人IgG缀合物。两种缀合物均显示出对IgG1和IgG3的高反应性,而对IgG2和IgG4的反应性较低。结论:这些结果表明以下因素可导致某些BP患者DIF上的IgG假阴性染色:(i):皮肤样本中的亚阈值IgG; (ii)商业抗人IgG缀合物与IgG4亚类的反应性有限; (iii)与双抗体法检测IgG相比,DIF的敏感性降低。使用夹心双抗体免疫荧光法检测IgG和/或IgG亚类可能有助于明确诊断IgG阴性且DIF上C3阳性的患者的BP。

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