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Why do I treat HBeAg-positive chronic hepatitis B patients with a nucleoside analogue
1Liver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Insights
Nucleos(t)ide analogues (NAs) effectively suppress chronic hepatitis B virus (HBV) DNA replication, improving liver histology and patient survival. Long-term NA therapy is crucial for managing CHB and preventing disease progression.
Area of Science:
- Hepatology
- Virology
- Pharmacology
Background:
- Chronic hepatitis B (CHB) poses a significant global health and economic challenge.
- Persistent hepatitis B virus (HBV) replication independently predicts disease progression.
- Sustained HBV replication suppression is key to preventing CHB progression and improving survival.
Purpose of the Study:
- To evaluate the efficacy and safety of nucleos(t)ide analogues (NAs) in managing CHB.
- To highlight the role of sustained viral suppression in achieving clinical benefits.
- To discuss treatment strategies for long-term HBV DNA suppression.
Main Methods:
- Review of pivotal clinical trials and real-world studies on NA treatment for CHB.
- Analysis of HBV DNA suppression rates, HBeAg seroconversion, and histological outcomes.
- Evaluation of NA safety profiles and resistance patterns.
Main Results:
- NAs demonstrate potent HBV DNA suppression with favorable safety profiles.
- Extended NA treatment increases HBeAg seroconversion rates.
- Profound HBV DNA suppression leads to histological improvement and reduced disease progression, even in cirrhosis.
Conclusions:
- NAs are the preferred first-line treatment for CHB due to high efficacy, safety, and proven clinical benefits.
- Long-term NA therapy can lead to sustained viral suppression and histological improvement.
- Treatment strategies should prioritize potent, low-resistance regimens for optimal long-term outcomes.
Abstract:
Chronic hepatitis B (CHB) is a worldwide public health problem which represents an enormous economic and social burden. Convincing evidence has shown that persistent active viral replication is an independent predictor of disease progression. Therefore, sustained suppression of HBV replication is the cornerstone for preventing the progression of disease and prolonging survival in patients with CHB. Pivotal clinical trials and real-world studies show that nucleos(t)ide analogues (NAs) are potent suppressors of HBV DNA replication with very good safety profiles. Although 1-year treatment with NAs only results in a modest rate of HBeAg seroconversion, extended treatment could increase this rate. Profound suppression of HBV DNA can result in histological improvement and a clinical benefit with a decrease in disease progression in patients with compensated or decompensated cirrhosis. Treatment must be begun with a highly potent and low resistant regimen to obtain long-term suppression of viral replication. An alternative solution may be a roadmap approach in which an inexpensive antiviral drug is started and another drug is added-on or switched-to if there is a suboptimal on-treatment decrease in HBV DNA. Clinical evidence has shown that once HBV DNA is suppressed and long-term HBeAg seroconversion is achieved, NAs can be stopped. In summary, high antiviral efficacy, excellent tolerance, extensive applicability, clearly proven histological improvement and long-term clinical benefit all make NAs the preferred choice for the management of CHB in most patients.
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