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Acute thrombocytopenia in patients treated with amiodarone is caused by antibodies specific for platelet membrane glycoproteins

机译:胺碘酮治疗的患者急性血小板减少症是由血小板膜糖蛋白特异性抗体引起的

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Summary: Amiodarone has been implicated as a cause of thrombocytopenia but the responsible mechanism is unknown. We performed studies in three patients to characterize the pathogenesis of this complication. No amiodarone-dependent, platelet-reactive antibodies were identified using conventional serological techniques. However, water-insoluble amiodarone solubilized in methanol and diluted to 1·0 mg/ml in aqueous buffer reproducibly promoted binding of IgG antibodies in patient serum to platelets. Solid phase assays identified drug-dependent antibodies specific for platelet glycoproteins (GP)Ia/IIa (integrin α2β1) in each patient and a second antibody specific for GPIIb/IIIa (αIIbβ3 integrin) in one patient. When studied by ion mobility analysis and transmission electron microscopy, the serologically active amiodarone preparation, a milky suspension, was found to consist of particles 2-30 nm in diameter, typical of a coacervate, a state characteristic of amiodarone in aqueous medium. The findings provide evidence that thrombocytopenia in the three patients studied was caused by drug-dependent antibodies specific for platelet glycoproteins GPIa/IIa and/or GPIIb/IIIa. We postulate that, in vivo, amiodarone may become incorporated into occult lipophilic domains in platelet glycoproteins, producing structural modifications that are immunogenic in some individuals, and that the resulting antibodies can cause platelet destruction in a person taking this drug.
机译:简介:胺碘酮已被认为是血小板减少症的病因,但其负责机制尚不清楚。我们对三名患者进行了研究,以表征这种并发症的发病机理。使用常规血清学技术未鉴定胺碘酮依赖性血小板反应性抗体。但是,不溶于水的胺碘酮可溶于甲醇,并在水性缓冲液中稀释至1·0 mg / ml,可再现地促进患者血清中IgG抗体与血小板的结合。固相分析在每位患者中鉴定了对血小板糖蛋白(GP)Ia / IIa(整合素α2β1)有特异性的药物依赖性抗体,在一位患者中对GPIIb / IIIa(αIIbβ3整合素)有特异性的第二种抗体。当通过离子迁移率分析和透射电子显微镜研究时,发现具有血清学活性的胺碘酮制剂(乳状悬浮液)由直径2-30 nm的颗粒组成,典型的凝聚层是胺碘酮在水性介质中的状态特征。这些发现提供了证据,表明三名患者的血小板减少症是由对血小板糖蛋白GPIa / IIa和/或GPIIb / IIIa特异性的药物依赖性抗体引起的。我们推测,在体内,胺碘酮可能会掺入血小板糖蛋白的隐性亲脂性结构域中,从而在某些个体中产生具有免疫原性的结构修饰,并且所得抗体会导致服用该药的人的血小板破坏。

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