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The natural course of chronic hepatitis B virus infection and its management
Stephanos J Hadziyannis1, Dimitrios Vassilopoulos, Emilia Hadziyannis
1Department of Medicine and Hepatology, Henry Dunant Hospital, Athens, Greece. hadziyannis@ath.forthnet.gr
Insights
Chronic hepatitis B (CHB) treatment focuses on suppressing hepatitis B virus (HBV) replication using drugs like entecavir and tenofovir. While effective, complete cure remains challenging, necessitating further research for new therapies.
Area of Science:
- Hepatology
- Virology
- Pharmacology
Background:
- Chronic hepatitis B virus (HBV) infection can lead to severe liver disease, including cirrhosis, decompensation, and hepatocellular carcinoma.
- Understanding the natural history and contributing factors is crucial for effective therapeutic intervention.
Purpose of the Study:
- To review current treatment strategies for chronic hepatitis B (CHB).
- To evaluate the efficacy and outcomes of first-line therapies, including pegylated interferon-α2a, entecavir, and tenofovir.
- To discuss the potential for achieving clinical cure and the limitations of current treatments.
Main Methods:
- Review of treatment protocols for CHB patients.
- Analysis of virological, serological, biochemical, and histological responses to therapy.
- Assessment of treatment outcomes during and after drug administration.
Main Results:
- Pegylated interferon-α2a, entecavir, and tenofovir are key first-line treatments for CHB.
- Entecavir and tenofovir show high potency, good safety, and a high barrier to resistance, representing significant therapeutic advancements.
- Clinical cure (HBsAg loss) is infrequent, and complete HBV eradication is currently unrealistic.
Conclusions:
- Current therapies effectively suppress HBV replication but rarely achieve a complete cure.
- New multi-target agents are needed to improve efficacy and potentially achieve a cure for CHB.
- Optimizing treatment requires understanding viral, host, and environmental factors.
Abstract:
Chronic infection with the hepatitis B virus (HBV) runs a long natural course during which underlying changes in liver histology can progress to cirrhosis and hepatic decompensation, as well as to hepatocellular carcinoma. Therapeutic intervention is currently aiming at suppression of HBV replication by applying a number of pharmacological agents. For an optimum use of available therapies, good knowledge of the natural course of chronic infection, as well as of the role played by several viral, host, and environmental factors, is mandatory. The larger part of this chapter deals with how to treat the various subsets of patients with chronic hepatitis B (CHB), using mainly three first-line drugs: pegylated interferon-α2a, entecavir, and tenofovir, administered either in finite courses or indefinitely. The frequency of virological, serological, biochemical, and histological responses in the various subsets of patients, both during and after stopping treatment, is reviewed. It is stressed that the application of the highly potent antivirals entecavir and tenofovir, with acceptable safety records and with a high barrier to HBV resistance, represents major progress in the treatment of CHB. Despite the hitherto important developments in the treatment of viral hepatitis B, clinical cure of chronic HBV infection with HBsAg loss is achievable only in a few treated patients while eradication of HBV infection appears unrealistic. Development of new pharmacological agents acting at multiple targets of the replicative cycle of HBV may achieve higher efficacy and even cure of CHB.
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