Treatment of chronic hepatitis B: From research to clinical practice via the consensus conferences

被引:16
作者
Brunetto, MR
Bonino, F
机构
[1] Azienda Osped Pisana, UO Gastroenterol & Epatol, I-56124 Pisa, Italy
[2] Osped Maggiore Milano, Policlin, IRCCS, Milan, Italy
关键词
chronic hepatitis B; treatment; drug resistance; interferon; nucleoside analogues;
D O I
10.2174/1381612043384277
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of antiviral therapy of chronic hepatitis B is to control Hepatitis B Virus (HBV) replication and to Cure liver disease avoiding the progression of chronic hepatitis to cirrhosis and the end stage complications of cirrhosis. HBeAg/anti-HBe seroconversion is the hallmark of response in hepatitis B "c" antigen (HBeAg) positive patients. In the patients with antibody against HBeAg (anti-HBe positive) the combination of HBV DNA and anti-HBc IgM tests provides adequate diagnostic accuracy. Patients with biochemical and/or histological disease activity are eligible to therapy. The drug choice is based on age, disease severity, risk of complications, side effects and compliance. particularly, in anti-HBe positive patients where prolonged treatment is needed. Interferon (5-6 MU daily or 9-10 MU thrice weekly for 4-6 months) is the first line therapy for HBcAg positive patients and (5-6 MU thrice weekly for 12-24 months) for anti-HBc positive patients. When IFN is contraindicated or ineffective, Lamivudine (100 mg) or Adefovir Dipivoxil (10 mg) are given as long as 4-6 months after HBeAg/anti-HBe seroconversion or for long-term treatments in HBeAg positive non-responders and anti-HBe positive patients. Patients with more advanced forms of cirrhosis and portal hypertension are to be treated within liver transplantation programs. Fifteen to 30% of treated patients achieve sustained response and more than 60% of them experience long-term disease remission during therapy. In perspectives, currently available molecular and immunologic tools and modelling of viral dynamics will help to address the therapy issue with more complex, efficacious and individually tailored treatment schedules.
引用
收藏
页码:2063 / 2075
页数:13
相关论文
共 99 条
[1]   MECHANISMS OF CLASS-I RESTRICTED IMMUNOPATHOLOGY - A TRANSGENIC MOUSE MODEL OF FULMINANT-HEPATITIS [J].
ANDO, K ;
MORIYAMA, T ;
GUIDOTTI, LG ;
WIRTH, S ;
SCHREIBER, RD ;
SCHLICHT, HJ ;
HUANG, SN ;
CHISARI, FV .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (05) :1541-1554
[2]   Resistance to adefovir dipivoxil therapy associated with the selection of a novel mutation in the HBV polymerase [J].
Angus, P ;
Vaughan, R ;
Xiong, S ;
Yang, HL ;
Delaney, W ;
Gibbs, C ;
Brosgart, C ;
Colledge, D ;
Edwards, R ;
Ayres, A ;
Bartholomeusz, A ;
Locarnini, S .
GASTROENTEROLOGY, 2003, 125 (02) :292-297
[3]   Lamivudine and Famciclovir resistant hepatitis B virus associated with fatal hepatic failure [J].
Ayres, A ;
Bartholomeusz, A ;
Lau, GKK ;
Lam, KC ;
Lee, JY ;
Locarnini, S .
JOURNAL OF CLINICAL VIROLOGY, 2003, 27 (01) :111-116
[4]   Long-term efficacy of interferon alpha-2b and lamivudine in combination compared to lamivudine monotherapy in patients with chronic hepatitis B. An Italian multicenter, randomized trial [J].
Barbaro, G ;
Zechini, F ;
Pellicelli, AM ;
Francavilla, R ;
Scotto, G ;
Bacca, D ;
Bruno, M ;
Babudieri, S ;
Annese, M ;
Matarazzo, F ;
Di Stefano, G ;
Barbarini, G .
JOURNAL OF HEPATOLOGY, 2001, 35 (03) :406-411
[5]   Kinetics of the immune response during HBV and HCV infection [J].
Bertoletti, A ;
Ferrari, C .
HEPATOLOGY, 2003, 38 (01) :4-13
[6]   Lamivudine treatment can overcome cytotoxic T-cell hyporesponsiveness in chronic hepatitis B: New perspectives for immune therapy [J].
Boni, C ;
Penna, A ;
Ogg, GS ;
Bertoletti, A ;
Pilli, M ;
Cavallo, C ;
Cavalli, A ;
Urbani, S ;
Boehme, R ;
Panebianco, R ;
Fiaccadori, F ;
Ferrari, C .
HEPATOLOGY, 2001, 33 (04) :963-971
[7]   Lamivudine treatment can restore T cell responsiveness in chronic hepatitis B [J].
Boni, C ;
Bertoletti, A ;
Penna, A ;
Cavalli, A ;
Pilli, M ;
Urbani, S ;
Scognamiglio, P ;
Boehme, R ;
Panebianco, R ;
Fiaccadori, F ;
Ferrari, C .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (05) :968-975
[8]   HEPATITIS-B VIRUS-DNA IN THE SERA OF HBSAG-CARRIERS - A MARKER OF ACTIVE HEPATITIS-B VIRUS-REPLICATION IN THE LIVER [J].
BONINO, F ;
HOYER, B ;
NELSON, J ;
ENGLE, R ;
VERME, G ;
GERIN, J .
HEPATOLOGY, 1981, 1 (05) :386-391
[9]   Outcome of anti-HBe positive chronic hepatitis B in alpha-interferon treated and untreated patients: a long term cohort study [J].
Brunetto, MR ;
Oliveri, F ;
Coco, B ;
Leandro, G ;
Colombatto, P ;
Gorin, JM ;
Bonino, F .
JOURNAL OF HEPATOLOGY, 2002, 36 (02) :263-270
[10]  
BRUNETTO MR, 1989, ITAL J GASTROENTEROL, V21, P151