deLemos Andrew S, Foureau David M, Jacobs Carl, Ahrens Will, Russo Mark W, Bonkovsky Herbert L
Department of Medicine, Center for Liver Diseases and Transplantation, Carolinas Medical Center, Charlotte, North Carolina.
Immune Monitoring Core Laboratory, Carolinas Medical Center, Charlotte, North Carolina.
Semin Liver Dis. 2014 May;34(2):194-204. doi: 10.1055/s-0034-1375959. Epub 2014 May 31.
Drug-induced liver injury (DILI) with features of autoimmunity (AI) represents an important category of hepatotoxicity due to medication exposure. Drugs repeatedly associated with AI-DILI include diclofenac, α-methyl DOPA, hydralazine, nitrofurantoin, minocycline, and more recently statins and anti-TNF-α agents. Usually, symptoms of acute liver injury occur within a few months after initiation of a culprit medication, but a longer latency period is possible. Like idiopathic autoimmune hepatitis, circulating autoantibodies and a hypergammaglobulinemia are frequently present in sera from patients with AI-DILI. If performed, a liver biopsy should demonstrate interface hepatitis with a prominent plasma cell infiltrate. The severity of AI-DILI is variable, but a complete resolution after withdrawal of the offending medication is the expectation. A response to corticosteroid therapy supports the diagnosis, whereas a lack of recurrence of symptoms or signs following corticosteroid cessation distinguishes AI-DILI from idiopathic autoimmune hepatitis.
具有自身免疫(AI)特征的药物性肝损伤(DILI)是药物暴露所致肝毒性的一个重要类别。反复与AI-DILI相关的药物包括双氯芬酸、α-甲基多巴、肼屈嗪、呋喃妥因、米诺环素,以及最近的他汀类药物和抗TNF-α药物。通常,急性肝损伤症状在可疑药物开始使用后的几个月内出现,但也可能有更长的潜伏期。与特发性自身免疫性肝炎一样,AI-DILI患者的血清中经常存在循环自身抗体和高球蛋白血症。如果进行肝活检,应显示界面性肝炎伴显著的浆细胞浸润。AI-DILI的严重程度各不相同,但停用致病药物后有望完全缓解。对皮质类固醇治疗有反应支持诊断,而停用皮质类固醇后症状或体征不再复发则可将AI-DILI与特发性自身免疫性肝炎区分开来。