Immune-mediated liver dysfunction after antiviral treatment in liver transplanted patients with hepatitis c: Allo or autoimmune de novo hepatitis?

被引:22
作者
Merli, A.
Gentili, F.
Giusto, M.
Attili, A. F.
Corradini, S. G.
Mennini, G.
Rossi, M.
Corsi, A. [1 ]
Bianco, P. [1 ]
机构
[1] Univ Roma La Sapienza, Policlin Umberto I, Ist Anat Patol, Rome, Italy
关键词
Autoimmune hepatitis; Hepatitis HCV; Liver transplantation; ALLOGRAFT DYSFUNCTION; THERAPY; RECURRENCE; RECIPIENTS; REJECTION; DIAGNOSIS; RIBAVIRIN;
D O I
10.1016/j.dld.2008.09.015
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background. The recurrence of hepatitis C after liver transplantation is extremely frequent. Antiviral therapy combining pegylated-interferon with ribavirin is therefore increasingly used in these patients. It has been recently reported, however, that during antiviral treatment a hepatic immune-mediated liver dysfunction, similar to "de novo" autoimmune hepatitis, may develop ill a few transplanted patients. Patients and methods. Three patients, treated with pegylated-interferon alpha-2a and ribavirin for recurrent hepatitis C after liver transplantation, developed an aggressive hepatitis with clinical, biochemical, and histological features similar to those of autoimmune hepatitis. Results. In all three patients, a liver enzymes increase was evident after hepatitis C virus-RNA had become undetectable. Diagnosis of "de novo" autoimmune hepatitis was proposed, based on the presence of high-titre circulating autoantibodies and liver histology features. Following the introduction of a steroid therapy, clinical and biochemical parameters progressively improved. Hepatitis C virus infection, however, relapsed after a few months in all the patients. Conclusions. Following liver transplantation, antiviral therapy with pegylated-interferon alpha-2a and ribavirin for recurrent hepatitis C may be associated, in a few patients, with severe immune-mediated graft dysfunction similar to autoimmune hepatitis. (C) 2008 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:345 / 349
页数:5
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