Isern R A, Yaneva M, Weiner E, Parke A, Rothfield N, Dantzker D, Rich S, Arnett F C
Department of Internal Medicine, University of Texas Medical School, Houston 77225.
Am J Med. 1992 Sep;93(3):307-12. doi: 10.1016/0002-9343(92)90238-7.
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.
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.
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.
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.
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。
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。
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。
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。