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头孢曲松可导致药物性免疫性血小板减少症和溶血性贫血:血小板和红细胞上靶点的特征分析

Ceftriaxone causes drug-induced immune thrombocytopenia and hemolytic anemia: characterization of targets on platelets and red blood cells.

作者信息

Grossjohann Beatrice, Eichler Petra, Greinacher Andreas, Santoso Sentot, Kroll Hartmut

机构信息

Institute for Immunology and Transfusion Medicine, Ernst Moritz Arndt University Greifswald, Germany.

出版信息

Transfusion. 2004 Jul;44(7):1033-40. doi: 10.1111/j.1537-2995.2004.03378.x.

Abstract

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.

摘要

背景

头孢曲松是一种第三代头孢菌素,据报道偶尔会导致致命的药物性免疫性溶血性贫血(DIHA)。本文报告了首例因头孢曲松导致严重药物性血小板减少症(DITP)的两名患者以及一名致命性DIHA患者的临床和血清学分析。

研究设计与方法

使用表达糖蛋白(GP)IIb/IIIa和GPIb/IX的转染细胞以及不同的头孢菌素,通过间接抗球蛋白试验(IAT)、酶免疫分析(EIA)、GP特异性免疫分析、流式细胞术和免疫沉淀法对血清进行评估。

结果

患者1和患者2的血清在药物存在的情况下与血小板发生强烈反应,但与红细胞无反应。药物依赖性抗体(DDAbs)的结合位点分别定位于GPIIb/IIIa和GPIb/IX。抑制研究表明,DDAbs分别识别位于GPIIb/IIIa复合物和GPIX亚基上的表位。未观察到与其他头孢菌素衍生物的交叉反应。血清3在头孢曲松的体外代谢产物存在的情况下与Rh(null)表型的红细胞发生强烈凝集,但与血小板无交叉反应。

结论

报告了首例严重DITP的两例病例以及一例DIHA患者。所有患者的DDAbs均表现出个体反应模式和明确的细胞系特异性。此外,DDAbs依赖于头孢曲松分子3位的取代。GPIIb/IIIa和GPIX上的表位与血小板有关。Rh蛋白不是红细胞上DDAbs的唯一靶点。

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