异烟肼
肝损伤
医学
CYP2E1
抗体
免疫系统
药理学
CYP3A4型
肝炎
肝病学
药品
免疫学
内科学
细胞色素P450
胃肠病学
病理
新陈代谢
肺结核
作者
Imir G. Metushi,Corron Sanders,William M. Lee,Jack Uetrecht
出处
期刊:Hepatology
[Lippincott Williams & Wilkins]
日期:2013-06-14
卷期号:59 (3): 1084-1093
被引量:133
摘要
UNLABELLED: Isoniazid (INH)-induced hepatotoxicity remains one of the most common causes of drug-induced idiosyncratic liver injury and liver failure. This form of liver injury is not believed to be immune-mediated because it is not usually associated with fever or rash, does not recur more rapidly on rechallenge, and previous studies have failed to identify anti-INH antibodies (Abs). In this study, we found Abs present in sera of 15 of 19 cases of INH-induced liver failure. Anti-INH Abs were present in 8 sera; 11 had anti-cytochrome P450 (CYP)2E1 Abs, 14 had Abs against CYP2E1 modified by INH, 14 had anti-CYP3A4 antibodies, and 10 had anti-CYP2C9 Abs. INH was found to form covalent adducts with CYP2E1, CYP3A4, and CYP2C9. None of these Abs were detected in sera from INH-treated controls without significant liver injury. The presence of a range of antidrug and autoAbs has been observed in other drug-induced liver injury that is presumed to be immune mediated. CONCLUSION: These data provide strong evidence that INH induces an immune response that causes INH-induced liver injury.
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