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原发性胆汁性肝硬化患者自身抗体的靶血小板抗原

Target platelet antigens of autoantibodies in patients with primary biliary cirrhosis.

作者信息

Feistauer S M, Penner E, Mayr W R, Panzer S

机构信息

Clinical Department for Blood Group Serology, University of Vienna, Austria.

出版信息

Hepatology. 1997 Jun;25(6):1343-5. doi: 10.1002/hep.510250607.

Abstract

Primary biliary cirrhosis (PBC) is an autoimmune disease of the liver, frequently associated with thrombocytopenia. As various immune abnormalities have been described in PBC, we hypothesized that thrombocytopenia is also an autoimmune phenomenon in these patients. We therefore assessed the frequency of platelet antibodies and their target platelet glycoprotein (GP) specificities. We investigated 66 PBC patients with a median disease duration of 25 months. Twenty-two patients with alcoholic liver disease and thrombocytopenia served as controls. Specificities of platelet antibodies were determined by the monoclonal antibody-specific immobilization of platelet antigens (MAIPA) assay using monoclonal antibodies directed against GPIIb/IIIa and GPIb/IX. The notion that immunoglobulins are nonspecifically bound to platelets was further evaluated by the production of eluates from antibody-coated platelets. The specificities of antibodies in these eluates were again determined by the MAIPA assay. Twenty-six PBC patients had platelet antibodies, whereas antibodies were not detectable in control alcoholic patients. Seven of 13 thrombocytopenic PBC patients had detectable antibodies. Overall, GP Ib/IX and GP IIb/IIIa served in a similar frequency as target antigens. Antibody specificities were confirmed by the production of eluates from platelets. These studies provide evidence that antibodies are specifically bound to platelets in patients with PBC and that the development of immune phenomena in PBC may also involve immuno-mediated platelet destruction.

摘要

原发性胆汁性肝硬化(PBC)是一种肝脏自身免疫性疾病,常伴有血小板减少。由于PBC中已描述了各种免疫异常,我们推测血小板减少在这些患者中也是一种自身免疫现象。因此,我们评估了血小板抗体的频率及其靶血小板糖蛋白(GP)特异性。我们调查了66例PBC患者,疾病中位病程为25个月。22例患有酒精性肝病和血小板减少的患者作为对照。使用针对GPIIb/IIIa和GPIb/IX的单克隆抗体,通过单克隆抗体特异性血小板抗原固定(MAIPA)试验确定血小板抗体的特异性。通过从抗体包被的血小板中产生洗脱液,进一步评估免疫球蛋白非特异性结合血小板的观点。这些洗脱液中抗体的特异性再次通过MAIPA试验确定。26例PBC患者有血小板抗体,而对照酒精性患者未检测到抗体。13例血小板减少的PBC患者中有7例可检测到抗体。总体而言,GP Ib/IX和GP IIb/IIIa作为靶抗原的频率相似。通过从血小板中产生洗脱液证实了抗体特异性。这些研究提供了证据,表明PBC患者的抗体与血小板特异性结合,且PBC中免疫现象的发生可能也涉及免疫介导的血小板破坏。

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