Grossjohann Beatrice, Eichler Petra, Greinacher Andreas, Santoso Sentot, Kroll Hartmut
Institute for Immunology and Transfusion Medicine, Ernst Moritz Arndt University Greifswald, Germany.
Transfusion. 2004 Jul;44(7):1033-40. doi: 10.1111/j.1537-2995.2004.03378.x.
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.
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.
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.
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.
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。
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。
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。
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。