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一名患有雷尼替丁诱导的血小板减少症患者的抗体识别糖蛋白IX上的一个位点,该位点是药物诱导抗体的首选靶点。

An antibody from a patient with ranitidine-induced thrombocytopenia recognizes a site on glycoprotein IX that is a favored target for drug-induced antibodies.

作者信息

Gentilini G, Curtis B R, Aster R H

机构信息

Department of Medicine, Medical College of Wisconsin and the Blood Research Institute, The Blood Center of Southeastern Wisconsin, Milwaukee, WI 53226-3548, USA.

出版信息

Blood. 1998 Oct 1;92(7):2359-65.

PMID:9746775
Abstract

Although thrombocytopenia associated with the use of histamine H2 receptor (H2R) antagonists has been described, a drug-dependent, platelet-reactive antibody has not previously been identified in such cases. We studied serum from a patient who developed acute, severe thrombocytopenia after exposure to the H2 receptor antagonist, ranitidine, and identified an antibody that reacted with normal platelets in the presence of this drug at pharmacologic concentrations. In flow cytometric and immunoprecipitation studies, the antibody was shown to be specific for the glycoprotein Ib/IX complex (GPIb/IX). From the pattern of monoclonal antibody (MoAb) inhibition and the reactions of antibody with Chinese hamster ovary (CHO) cells transfected with GPIX and GPIbbeta, we found that the patient's antibody is specific for an epitope on GPIX close to, or identical with a site recognized by the MoAb SZ1 that is a common target for antibodies induced by quinine and quinidine, drugs structurally unrelated to ranitidine. These findings provide evidence that immune thrombocytopenia can be caused by sensitivity to an H2 R antagonist and suggest that the SZ1 binding site on GPIX may be a common target for drug-induced antibodies. Further studies of the epitope for which SZ1 is specific may provide clues to the mechanism(s) by which drugs promote tight binding of antibody to a membrane glycoprotein and cause platelet destruction in patients with drug sensitivity.

摘要

尽管使用组胺H2受体(H2R)拮抗剂相关的血小板减少症已有报道,但此前在此类病例中尚未鉴定出药物依赖性血小板反应性抗体。我们研究了一名患者的血清,该患者在接触H2受体拮抗剂雷尼替丁后发生急性、严重血小板减少症,并鉴定出一种在该药物处于药理浓度时与正常血小板发生反应的抗体。在流式细胞术和免疫沉淀研究中,该抗体显示对糖蛋白Ib/IX复合物(GPIb/IX)具有特异性。根据单克隆抗体(MoAb)抑制模式以及抗体与转染了GPIX和GPIbbeta的中国仓鼠卵巢(CHO)细胞的反应,我们发现患者的抗体对GPIX上靠近或与MoAb SZ1识别位点相同的一个表位具有特异性,MoAb SZ1是由奎宁和奎尼丁诱导的抗体的常见靶点,奎宁和奎尼丁在结构上与雷尼替丁无关。这些发现提供了证据,表明免疫性血小板减少症可由对H2R拮抗剂的敏感性引起,并提示GPIX上的SZ1结合位点可能是药物诱导抗体的常见靶点。对SZ1特异性表位的进一步研究可能为药物促进抗体与膜糖蛋白紧密结合并导致药物敏感性患者血小板破坏的机制提供线索。

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