Eliasson E, Stål P, Oksanen A, Lytton S
Division of Molecular Toxicology, Institute of Environmental Medicine, Karolinska Institute, Stockholm, Sweden.
J Hepatol. 1998 Nov;29(5):819-25. doi: 10.1016/s0168-8278(98)80264-x.
BACKGROUND/AIMS: Immunological mechanisms are involved in many adverse drug reactions. In certain forms of drug-induced hepatitis, patients have been reported to express specific autoantibodies to hepatic drug-metabolising enzymes. The alcohol deterrent disulfiram is associated with a low frequency of severe liver toxicity, including hepatitis, but the mechanism of the toxicity is unknown. We investigated whether autoantibodies to cytochrome P450 enzymes were expressed in the serum of a 28-year-old male patient, who developed hepatitis after 7 weeks of disulfiram treatment and in whom possible causes of hepatitis other than disulfiram had been ruled out.
Patient serum IgG reactivity was analysed by immunoblotting or ELISA against test antigens consisting of recombinant/purified human or rat liver P450 enzymes, or isolated rat liver microsomes.
A significant serum reactivity was found in immunoblotting against human cytochromes P450 1A2 and rat P450 3A1, using serum dilutions of up to 1:900 and 1:2400, respectively. In contrast, the reactivity against cytochromes P450 2E1, 2C9, 2D6, 3A4, and rat liver P450 reductase was either very low or undetectable. ELISA reactivity was low in general, indicating that the P450 epitopes were not surface exposed. Immunoblotting of rat liver microsomes revealed that autoantibodies recognised one major polypeptide corresponding to P450 3A. Autoantibody titres remained stable for at least 6 months after acute hepatitis. A similar reactivity was not found in any of ten control sera.
The expression of autoantibodies directed against specific cytochromes P450 in a case of disulfiram hepatitis suggests that immunological mechanisms are involved in this adverse drug reaction, and that these P450 proteins should be evaluated as possible diagnostic test antigens in disulfiram hepatotoxicity.
背景/目的:免疫机制参与了许多药物不良反应。在某些形式的药物性肝炎中,有报道称患者会表达针对肝脏药物代谢酶的特异性自身抗体。戒酒药双硫仑与包括肝炎在内的严重肝毒性的低发生率相关,但毒性机制尚不清楚。我们调查了一名28岁男性患者的血清中是否表达了细胞色素P450酶自身抗体,该患者在双硫仑治疗7周后出现肝炎,且已排除双硫仑以外可能导致肝炎的原因。
通过免疫印迹法或酶联免疫吸附测定(ELISA)分析患者血清IgG对由重组/纯化的人或大鼠肝脏P450酶或分离的大鼠肝脏微粒体组成的测试抗原的反应性。
在免疫印迹法中,分别使用高达1:900和1:2400的血清稀释度时,发现血清对人细胞色素P450 1A2和大鼠P450 3A1有显著反应性。相比之下,对细胞色素P450 2E1、2C9、2D6、3A4和大鼠肝脏P450还原酶的反应性要么非常低,要么无法检测到。ELISA反应性总体较低,表明P450表位未暴露于表面。大鼠肝脏微粒体的免疫印迹显示自身抗体识别一种与P450 3A相对应的主要多肽。急性肝炎后自身抗体滴度至少6个月保持稳定。在10份对照血清中均未发现类似反应性。
在一例双硫仑肝炎病例中,针对特定细胞色素P450的自身抗体的表达表明免疫机制参与了这种药物不良反应,并且这些P450蛋白应作为双硫仑肝毒性可能的诊断测试抗原进行评估。