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,Anne M. Larson,Iris Liou,Timothy J. Davern,Oren K. Fix,Michael L. Schilsky,Timothy M. McCashland,J. Eileen Hay,Natalie Murray,A. Obaid S. Shaikh,Andrés T. Blei,Daniel Ganger,Atif Zaman,Steven Han,Robert J. Fontana,Brendan M. McGuire,Raymond T. Chung,Alastair D. Smith
出处
期刊:Hepatology
[Lippincott Williams & Wilkins]
日期:2013-06-14
卷期号:59 (3): 1084-1093
被引量:121
摘要
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. (Hepatology 2014;59:1084–1093)
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