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自身免疫性垂体炎中的新型自身抗原。

Novel autoantigens in autoimmune hypophysitis.

作者信息

Lupi Isabella, Broman Karl W, Tzou Shey-Cherng, Gutenberg Angelika, Martino Enio, Caturegli Patrizio

机构信息

Department of Pathology, The Johns Hopkins University, School of Medicine, Baltimore, MD 21205, USA.

出版信息

Clin Endocrinol (Oxf). 2008 Aug;69(2):269-78. doi: 10.1111/j.1365-2265.2008.03180.x. Epub 2008 Jan 10.

Abstract

BACKGROUND

Pituitary autoantibodies are found in autoimmune hypophysitis and other conditions. They are a marker of pituitary autoimmunity but currently have limited clinical value. The methods used for their detection lack adequate sensitivity and specificity, mainly because the pathogenic pituitary autoantigen(s) are not known and therefore antigen-based immunoassays have not been developed.

OBJECTIVES

This study aimed to identify novel pituitary autoantigens using sera as probes in proteomic assays. We also compared immunoblotting and immunofluorescence methods for their accuracy in diagnosing autoimmune hypophysitis.

STUDY DESIGN AND SUBJECTS

Twenty-eight sera from autoimmune hypophysitis cases (14 histologically proven and 14 clinically suspected) were compared to 98 sera from controls, which included 14 patients with pituitary adenomas, 48 with autoimmune thyroiditis (15 Graves' disease and 33 Hashimoto's thyroiditis) and 36 healthy subjects.

METHODS

All sera were tested against human pituitary cytosolic proteins separated by one-dimensional (1D) gel electrophoresis. The band recognition was analysed statistically to detect molecular weight regions preferentially recognized by hypophysitis sera. 2D gel immunoblotting and mass spectrometry were then used to sequence the protein spots of interest. Sera were also tested by immunofluorescence for their recognition of Macaca mulatta pituitary sections.

RESULTS

A single region in the 25-27-kDa range was recognized more often by hypophysitis cases than healthy subjects (P = 0.004) or patients with pituitary adenomas (P = 0.044). This region contained two novel candidate autoantigens: chromosome 14 open reading frame 166 (C14orf166) and chorionic somatomammotrophin. Immunoblotting positivity for the 25-27-kDa region yielded greater sensitivity (64%vs. 57%) and specificity (86%vs. 76%) than immunofluorescence in predicting histologically proven hypophysitis, although the performance was still inadequate to make immunoblotting a clinically useful test.

CONCLUSION

The study reports two novel proteins that could act as autoantigens in autoimmune hypophysitis. Further studies are needed to validate their pathogenic role and diagnostic utility.

摘要

背景

垂体自身抗体见于自身免疫性垂体炎及其他病症。它们是垂体自身免疫的标志物,但目前临床价值有限。用于检测它们的方法缺乏足够的敏感性和特异性,主要是因为致病性垂体自身抗原不明,因此基于抗原的免疫测定法尚未开发出来。

目的

本研究旨在利用血清作为蛋白质组学检测中的探针来鉴定新的垂体自身抗原。我们还比较了免疫印迹法和免疫荧光法在诊断自身免疫性垂体炎方面的准确性。

研究设计与对象

将28份自身免疫性垂体炎病例的血清(14份经组织学证实,14份临床疑似)与98份对照血清进行比较,对照血清包括14例垂体腺瘤患者、48例自身免疫性甲状腺炎患者(15例格雷夫斯病和33例桥本甲状腺炎)以及36名健康受试者。

方法

所有血清均针对通过一维(1D)凝胶电泳分离的人垂体胞质蛋白进行检测。对条带识别情况进行统计学分析,以检测垂体炎血清优先识别的分子量区域。然后使用二维凝胶免疫印迹法和质谱法对感兴趣的蛋白斑点进行测序。血清还通过免疫荧光法检测其对猕猴垂体切片的识别情况。

结果

垂体炎病例比健康受试者(P = 0.004)或垂体腺瘤患者(P = 0.044)更常识别25 - 27 kDa范围内的单个区域。该区域包含两种新的候选自身抗原:14号染色体开放阅读框166(C14orf166)和绒毛膜生长催乳素。在预测经组织学证实的垂体炎方面,25 - 27 kDa区域的免疫印迹阳性率比免疫荧光法具有更高的敏感性(64%对57%)和特异性(86%对76%),尽管其性能仍不足以使免疫印迹法成为一项临床有用的检测方法。

结论

该研究报告了两种可能在自身免疫性垂体炎中作为自身抗原的新蛋白。需要进一步研究来验证它们的致病作用和诊断效用。

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