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A Competent Hepatocyte Model Examining Hepatitis B Virus Entry through Sodium Taurocholate Cotransporting Polypeptide as a Therapeutic Target
Published on: May 10, 2022
Treatment of chronic hepatitis B: from research to clinical practice via the consensus conferences
1U.O. Gastroenterologia e Epatologia, Azienda Ospedaliera Pisana, Via Paradisa 2, 56124 Cisanello, Pisa, Italy. brunetto@med-club.com
Insights
Antiviral therapy for chronic hepatitis B aims to control Hepatitis B Virus (HBV) replication and prevent liver disease progression. Treatment choice depends on patient factors, with Interferon, Lamivudine, and Adefovir Dipivoxil being common options.
Area of Science:
- Hepatology
- Virology
- Pharmacology
Background:
- Chronic hepatitis B (CHB) management focuses on inhibiting Hepatitis B Virus (HBV) replication.
- Preventing CHB progression to cirrhosis and its complications is a primary therapeutic goal.
- HBeAg/anti-HBe seroconversion serves as a key indicator of treatment response in HBeAg-positive patients.
Purpose of the Study:
- To outline the objectives and strategies for antiviral therapy in chronic hepatitis B.
- To detail the diagnostic criteria and treatment eligibility for CHB patients.
- To describe the first-line and alternative pharmacological interventions for CHB.
Main Methods:
- Patient eligibility determined by biochemical and/or histological disease activity.
- Drug selection based on age, disease severity, complication risk, side effects, and compliance.
- Interferon (IFN) as first-line therapy; Lamivudine or Adefovir Dipivoxil as alternatives or for long-term treatment.
- Liver transplantation considered for advanced cirrhosis and portal hypertension.
Main Results:
- Sustained response achieved in 15-30% of treated patients.
- Over 60% experience long-term disease remission during therapy.
- Diagnostic accuracy in anti-HBe positive patients relies on HBV DNA and anti-HBc IgM tests.
Conclusions:
- Antiviral therapy effectively controls HBV replication and prevents disease progression.
- Tailored treatment schedules incorporating molecular and immunologic tools are future directions.
- Individualized treatment plans are crucial for optimizing outcomes in chronic hepatitis B management.
Abstract:
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 "e" 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 HBeAg positive patients and (5-6 MU thrice weekly for 12-24 months) for anti-HBe 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.
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