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可溶性核抗原特异性抗体的临床意义(作者译)

[The clinical significance of soluble nuclear antigen specific antibodies (author's transl)].

作者信息

Peltier A P, Gaudreau A, Amor B, Kahn M F, Ryckewaert A, Sany J, Haim T

出版信息

Nouv Presse Med. 1978 May 27;7(21):1813-8.

PMID:307737
Abstract

Anti-ENA antibodies have been found in 176 sera which nearly all contained antinuclear antibodies giving a speckled pattern of nuclear fluorescence. The charts of 134 of these 176 patients were available for a thorough clinical study. Among these 134 patients, 59 had a well defined Connective Tissue Disease including 40 SLE, 31 had a limited clinical syndrome made of Raynaud's phenomenon, inflammatory polyarthritis, swollen fingers and hyperglobulinemia and 34 had a complex clinical picture associating signs of more than one connective tissue disease. Some of the patients in this third group could be considered as-having the Mixed Connective Tissue Disease (MCTD) described by Sharp et al. Anti-RNP antibodies were more common in this series than the other anti-ENA antibodies. However, no narrow specificity could be assigned to any of these antibodies. This is true of the non anti-RNP antibodies, the anti-Sm in particular, which were found in 49 patients of whom 32 had SLE existing alone or in association with features of other connective tissue diseases and 17 had another connective tissue disease or the afore-mentioned limited clinical syndrome. In any case, the anti-ECT antibodies never reach the diagnostic value of the anti-DNA antibodies.

摘要

在176份血清中发现了抗可提取性核抗原(ENA)抗体,几乎所有这些血清都含有抗核抗体,呈现核荧光斑点型。这176例患者中有134例的病历可供进行全面的临床研究。在这134例患者中,59例患有明确的结缔组织病,其中40例为系统性红斑狼疮(SLE),31例有由雷诺现象、炎性多关节炎、手指肿胀和高球蛋白血症组成的局限性临床综合征,34例有涉及一种以上结缔组织病体征的复杂临床表现。第三组中的一些患者可被认为患有Sharp等人描述的混合性结缔组织病(MCTD)。在该系列中,抗核糖核蛋白(RNP)抗体比其他抗ENA抗体更常见。然而,这些抗体中没有一种具有明确的特异性。非抗RNP抗体,尤其是抗史密斯(Sm)抗体也是如此,在49例患者中发现了抗Sm抗体,其中32例单独患有SLE或合并其他结缔组织病特征,17例患有另一种结缔组织病或上述局限性临床综合征。无论如何,抗ECT抗体从未达到抗DNA抗体的诊断价值。

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