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原发性肺动脉高压患者的自身抗体:与抗Ku的关联。

Autoantibodies in patients with primary pulmonary hypertension: association with anti-Ku.

作者信息

Isern R A, Yaneva M, Weiner E, Parke A, Rothfield N, Dantzker D, Rich S, Arnett F C

机构信息

Department of Internal Medicine, University of Texas Medical School, Houston 77225.

出版信息

Am J Med. 1992 Sep;93(3):307-12. doi: 10.1016/0002-9343(92)90238-7.

Abstract

PURPOSE

Patients with primary pulmonary hypertension (PPH) frequently have Raynaud's phenomenon, serum antinuclear antibodies (ANAs), and/or pulmonary vascular lesions similar to those seen in certain connective tissue diseases, especially scleroderma. A number of relatively disease-specific autoantibodies have been described in connective tissue diseases but have not been studied in patients with PPH. Therefore, sera from PPH patients were studied for a variety of autoantibodies, seeking a possible link between this pulmonary disorder and connective tissue diseases.

PATIENTS AND METHODS

Sera from 31 patients with PPH and 24 with secondary pulmonary hypertension (SPH) were studied for the following autoantibodies: anti-centromere (indirect immunofluorescence of Hep-2 cells), anti-CENP-B by immunoblotting and enzyme immunoassay (EIA) using cloned CENP-B fusion protein, anti-topoisomerase I (Scl-70), anti-Ku using immunoblotting of affinity purified antigens, anti-cardiolipin using EIA, and anti-Ro (SS-A), La (SS-B), Sm, nRNP, Jo-1, PM-Scl, and Mi-2 by counter-current immunoelectrophoresis.

RESULTS

Anti-Ku antibodies were found in 23% of patients with PPH, 4% with SPH, and none of 24 normal controls (PPH versus SPH, p = 0.06: PPH versus controls, p = 0.01). Antibodies to CENP-B were found in one patient each with PPH and SPH, anti-topoisomerase I in one with SPH, and anti-Ro (SS-A) and La (SS-B) in one with PPH. Overall, 12 patients (39%) with PPH had Raynaud's phenomenon or positive ANA results, with 9 (29%) having more specific autoantibodies associated with connective tissue diseases.

CONCLUSIONS

These results further suggest a link between at least a subgroup of patients with PPH and autoimmune connective tissue diseases, with anti-Ku antibodies being a possible new serologic marker.

摘要

目的

原发性肺动脉高压(PPH)患者常出现雷诺现象、血清抗核抗体(ANA)和/或与某些结缔组织病(尤其是硬皮病)中所见相似的肺血管病变。在结缔组织病中已描述了许多相对疾病特异性的自身抗体,但尚未在PPH患者中进行研究。因此,对PPH患者的血清进行了多种自身抗体的研究,以寻找这种肺部疾病与结缔组织病之间可能的联系。

患者与方法

对31例PPH患者和24例继发性肺动脉高压(SPH)患者的血清进行了以下自身抗体检测:抗着丝点抗体(Hep-2细胞间接免疫荧光法)、使用克隆的CENP-B融合蛋白通过免疫印迹法和酶免疫测定(EIA)检测抗CENP-B抗体、抗拓扑异构酶I(Scl-70)、使用亲和纯化抗原的免疫印迹法检测抗Ku抗体、使用EIA检测抗心磷脂抗体,以及通过对流免疫电泳检测抗Ro(SS-A)、La(SS-B)、Sm、nRNP、Jo-1、PM-Scl和Mi-2抗体。

结果

23%的PPH患者、4%的SPH患者检测到抗Ku抗体,24例正常对照均未检测到(PPH与SPH相比,p = 0.06;PPH与对照相比,p = 0.01)。PPH和SPH各有1例患者检测到抗CENP-B抗体,1例SPH患者检测到抗拓扑异构酶I抗体,1例PPH患者检测到抗Ro(SS-A)和La(SS-B)抗体。总体而言,12例(39%)PPH患者有雷诺现象或ANA结果呈阳性,其中9例(29%)有与结缔组织病相关的更特异性自身抗体。

结论

这些结果进一步提示至少一部分PPH患者与自身免疫性结缔组织病之间存在联系,抗Ku抗体可能是一种新的血清学标志物。

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