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针对不同核基质蛋白的抗体是混合性结缔组织病的特征。

Antibodies against distinct nuclear matrix proteins are characteristic for mixed connective tissue disease.

作者信息

Habets W J, de Rooij D J, Salden M H, Verhagen A P, van Eekelen C A, van de Putte L B, van Venrooij W J

出版信息

Clin Exp Immunol. 1983 Oct;54(1):265-76.

Abstract

Specific nuclear proteins, separated according to their molecular weight (mol. wt) by polyacrylamide gel electrophoresis (PAGE) and subsequently transferred to nitrocellulose sheets, are able to bind antibodies in sera from patients suffering from different types of connective tissue diseases. Antibodies against a characteristic set of nuclear protein antigens are found in sera from patients with mixed connective tissue disease (MCTD). Screening of 21 MCTD sera revealed a typical immunoblot pattern with major protein antigens of mol. wt 70,000 (20/21) (not identical with the Scl-70 antigen characteristic for scleroderma), mol. wt 31,000 (17/21), two proteins around mol. wt 23,000 (15/21) and two around mol. wt 19,000 (10/21). The 70,000, 23,000 and 19,000 antigens appeared to be rather insoluble nuclear proteins (i.e. components of the nuclear matrix). On behalf of their structural character they were present in nuclei from several types of cells but only in low amounts detectable in salt extracts of thymus acetone powder. The presence of antibodies directed against the mol. wt 70,000 antigen correlated strongly with the diagnosis of MCTD. This 70,000 antigen is not identical with the RNP antigen, a soluble ribonuclease sensitive ribonucleoprotein, since antibodies against nuclear RNP can be separated from anti-nuclear matrix antibodies by affinity chromatography using immobilized thymus salt extract. The distinct character of soluble nuclear RNP and structural nuclear matrix antigens is further supported by the fact that from 14 other anti-RNP sera obtained from patients with systemic lupus erythematosus (SLE), only three contained antibodies against the mol. wt 70,000 protein. Since the immunoblot pattern obtained with MCTD sera mostly was clearly distinguishable from the patterns obtained with sera from patients with related connective tissue diseases our results suggest that the immunoblotting technique might be useful as a diagnostic tool and support the concept of MCTD as a distinct entity.

摘要

特定的核蛋白,通过聚丙烯酰胺凝胶电泳(PAGE)根据其分子量进行分离,随后转移至硝酸纤维素膜上,能够与患有不同类型结缔组织病患者血清中的抗体结合。在混合性结缔组织病(MCTD)患者的血清中发现了针对一组特征性核蛋白抗原的抗体。对21份MCTD血清进行筛查,发现了一种典型的免疫印迹模式,主要蛋白抗原的分子量分别为70,000(20/21)(与硬皮病特有的Scl-70抗原不同)、31,000(17/21)、两种分子量约为23,000的蛋白(15/21)以及两种分子量约为19,000的蛋白(10/21)。分子量为70,000、23,000和19,000的抗原似乎是相当不溶性的核蛋白(即核基质的成分)。就其结构特征而言,它们存在于几种类型细胞的细胞核中,但仅在胸腺丙酮粉的盐提取物中可检测到少量。针对分子量为70,000抗原的抗体的存在与MCTD的诊断密切相关。这种分子量为70,000的抗原与RNP抗原不同,RNP抗原是一种可溶性的对核糖核酸酶敏感的核糖核蛋白,因为针对核RNP的抗体可以通过使用固定化胸腺盐提取物的亲和层析与抗核基质抗体分离。可溶性核RNP和结构性核基质抗原的不同特征进一步得到以下事实的支持:从14份来自系统性红斑狼疮(SLE)患者的其他抗RNP血清中,只有三份含有针对分子量为70,000蛋白的抗体。由于用MCTD血清获得的免疫印迹模式大多与用相关结缔组织病患者血清获得的模式明显不同,我们的结果表明免疫印迹技术可能作为一种诊断工具有用,并支持MCTD作为一个独特实体的概念。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610a/1536194/fefaede35553/clinexpimmunol00151-0279-a.jpg

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