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Development of a Hepatitis B Virus Reporter System to Monitor the Early Stages of the Replication Cycle
Published on: February 1, 2017
Recent developments in antivirals against hepatitis B virus
Ya-Juan Wang1, Li Yang1, Jian-Ping Zuo1
1Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Zuchongzhi Road 555, Shanghai, People's Republic of China.
Insights
New antivirals are needed to cure chronic hepatitis B (CHB) infection, as current treatments only suppress the virus and do not eradicate it. This review covers key developments in HBV replication inhibitors and immune regulators.
Area of Science:
- Hepatology
- Virology
- Immunology
Background:
- Chronic hepatitis B virus (CHB) infection is a significant global health issue, leading to cirrhosis and hepatocellular carcinoma (HCC).
- While HBV vaccines reduce new infections, the burden of existing CHB remains substantial.
- Current antiviral therapies, including nucleos(t)ide analogs like entecavir (ETV) and tenofovir disoproxil fumarate (TDF), effectively suppress viral replication but require lifelong treatment and cannot eliminate the virus.
Purpose of the Study:
- To review the latest advancements in antiviral therapies for chronic hepatitis B.
- To highlight novel strategies targeting HBV replication and host immune responses for a potential cure.
Main Methods:
- Literature review of recent developments in hepatitis B antivirals.
- Analysis of HBV replication cycle inhibitors.
- Examination of host immune-modulating agents for HBV treatment.
Main Results:
- Current first-line treatments (ETV, TDF) offer viral suppression but present challenges like cost and long-term adherence.
- No existing therapies can eradicate the intracellular HBV, indicating an unmet medical need.
- Emerging strategies focus on inhibiting viral replication and restoring host immunity.
Conclusions:
- There is a critical need for novel therapeutic strategies to achieve a functional cure for chronic hepatitis B.
- Inhibitors of HBV replication and host immune regulators represent promising avenues for future HBV cure development.
Abstract:
Chronic hepatitis B virus (HBV) infection (CHB) is a major cause of cirrhosis and hepatocellular carcinoma (HCC). Although the availability of HBV vaccines effectively reduces the incidence of HBV infection, the healthcare burden from CHB remains high. Several antiviral agents, such as (pegylated-) interferon-α and nucleos(t)ide analogs are approved by US FDA for chronic HBV infection management. Entecavir (ETV) and tenofovir disoproxil fumarate (TDF) have been recommended as the first-line anti-HBV drugs for excellent viral suppression with a low risk of antiviral resistance, but the cost and need for essentially life-long treatment are considerable challenges. And none of these current treatments can eradicate the intracellular virus. Given these issues, there is still an unmet medical need for an efficient HBV cure. We summarize here the key developments of antivirals against hepatitis B virus, including HBV replication cycle inhibitors and host immune regulators.
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