首页> 外文期刊>Transfusion: The Journal of the American Association of Blood Banks >Ceftriaxone causes drug-induced immune thrombocytopenia and hemolytic anemia: characterization of targets on platelets and red blood cells.
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Ceftriaxone causes drug-induced immune thrombocytopenia and hemolytic anemia: characterization of targets on platelets and red blood cells.

机译:头孢曲松钠引起药物引起的免疫性血小板减少和溶血性贫血:血小板和红细胞上靶标的表征。

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摘要

BACKGROUND: Ceftriaxone, a third-generation cephalosporin, has been reported to occasionally cause fatal drug-induced immune hemolytic anemia (DIHA). A clinical and serologic analysis of the first two patients with severe drug-induced thrombocytopenia (DITP) due to ceftriaxone and one patient with fatal DIHA is reported. STUDY DESIGN AND METHODS: Sera were assessed by the IAT, EIA, glycoprotein (GP)-specific immunoassay, flow cytometry, and immunoprecipitation using transfectants expressing GPIIb/IIIa and GPIb/IX and with different cephalosporins. RESULTS: Sera from Patients 1 and 2 reacted strongly with PLTs in the presence of the drug, but not with RBCs. The binding sites of the drug-dependent antibodies (DDAbs) could be localized to GPIIb/IIIa and GPIb/IX, respectively. Inhibition studies indicated that DDAbs recognized epitopes residing on the GPIIb/IIIa complex and on the GPIX subunit, respectively. No cross-reactivity was observed with other cephalosporin derivatives. Serum 3 showed strong agglutination with RBCs of Rh(null) phenotype in the presence of ex-vivo metabolites of ceftriaxone, but no cross-reactivity with PLTs. CONCLUSIONS: The first two cases of severe DITP and a third patient with DIHA are reported. DDAbs from all patients showed individual reaction patterns and clear cell lineage specificity. In addition, the DDAbs were dependent on the substitution at position 3 of the ceftriaxone molecule. Epitopes on GPIIb/IIIa and GPIX were involved on PLTs. The Rh protein was not the only target of DDAbs on RBCs.
机译:背景:头孢曲松是第三代头孢菌素,据报道偶尔会引起致命的药物性免疫溶血性贫血(DIHA)。据报道,对头两名因头孢曲松引起的严重药物性血小板减少症(DITP)和一名致命DIHA的患者进行了临床和血清学分析。研究设计和方法:使用表达GPIIb / IIIa和GPIb / IX以及不同头孢菌素的转染子,通过IAT,EIA,糖蛋白(GP)特异性免疫测定,流式细胞仪和免疫沉淀法评估血清。结果:患者1和2的血清在存在该药物的情况下与PLT强烈反应,但与RBC则无反应。药物依赖性抗体(DDAbs)的结合位点可以分别定位于GPIIb / IIIa和GPIb / IX。抑制研究表明,DDAbs分别识别GPIIb / IIIa复合体和GPIX亚基上的表位。与其他头孢菌素衍生物未观察到交叉反应。血清3在头孢曲松的离体代谢产物存在下与Rh(null)表型的RBC强烈凝集,但与PLT无交叉反应。结论:报道了头两例严重DITP和第三例DIHA患者。所有患者的DDAb均显示出各自的反应模式和明确的细胞谱系特异性。此外,DDAb依赖于头孢曲松钠分子3位的取代。 GPIIb / IIIa和GPIX上的表位与PLT有关。 Rh蛋白不是DDAbs在RBCs上的唯一靶标。

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