Related Experiment Video
Updated: May 7, 2026

Stem Cell-Derived Viral Ag-Specific T Lymphocytes Suppress HBV Replication in Mice
Published on: September 25, 2019
Long-term outcomes after nucleos(t)ide analogues discontinuation in chronic hepatitis B patients with HBeAg-negative
Dengming He1, Shimin Guo, Wen Chen
1Institute of Infectious Diseases, Southwest Hospital, Third Military Medical University, Chongqing, China. wym417@163.com.
Insights
Discontinuing nucleos(t)ide analogues (NUCs) is safe for Hepatitis B e Antigen-negative chronic hepatitis B (CHB) patients with undetectable HBV DNA. Prolonging therapy duration can reduce relapse rates, with over 96 weeks of sustained response predicting long-term success.
Area of Science:
- Hepatology
- Virology
- Internal Medicine
Background:
- Hepatitis B e Antigen (HBeAg)-negative chronic hepatitis B (CHB) signifies active liver disease with risks of cirrhosis and hepatocellular carcinoma.
- Management of HBeAg-negative CHB patients on nucleos(t)ide analogues (NUCs) requires careful consideration regarding treatment withdrawal.
Purpose of the Study:
- To evaluate the outcomes of HBeAg-negative CHB patients after discontinuing NUC therapy.
- To identify factors influencing relapse rates and long-term sustained response post-NUCs withdrawal.
Main Methods:
- A cohort of 66 HBeAg-negative CHB patients (2 with HBsAg loss, 64 with sustained undetectable HBV DNA) discontinued NUCs.
- Regular monitoring of HBV DNA and alanine aminotransferase (ALT) levels post-discontinuation.
- Relapse defined as HBV DNA >2,000 IU/mL on two occasions more than 4 weeks apart.
Main Results:
- No relapses occurred in patients who achieved HBsAg loss.
- Among patients with undetectable HBV DNA, 29.7% experienced relapse, all within 96 weeks.
- No significant differences in baseline characteristics or time to consolidation therapy were observed between relapse and sustained-response groups.
Conclusions:
- NUC discontinuation is feasible in HBeAg-negative CHB patients with undetectable HBV DNA.
- Extending the duration before consolidation therapy may lower relapse rates.
- Sustained response for over 96 weeks predicts long-term sustained virologic response.
Background:
Hepatitis B e Antigen (HBeAg)-negative chronic hepatitis B (CHB) patients have an active liver disease with a high risk of progression to decompensated cirrhosis and hepatocellular carcinoma. The management strategy for HBeAg-negative CHB patients treated with nucleos(t)ide analogues (NUCs) is a topic of concern. To observe the outcomes for this population after NUCs withdrawal, HBeAg-negative CHB patients with loss of hepatitis B surface antigen (HBsAg) or sustained undetectable HBV DNA levels who had discontinued NUCs therapy were included in the study.
Methods:
A total of 66 patients (2 patients with HBsAg loss and 64 patients with sustained undetectable HBV DNA levels) were examined. HBV DNA levels and alanine aminotransferase (ALT) levels were monitored regularly after discontinuation of NUCs therapy. Relapse was defined as HBV DNA levels >2,000 IU/mL while off therapy in at least two determinations more than 4 weeks apart.
Results:
The time to achieve undetectable HBV DNA levels was 14 weeks (interquartile range (IQR): 12-24 weeks). The time until consolidation therapy was 144 weeks (IQR: 96-168 weeks). No relapses occurred in either of the HBsAg loss patients. Among the 64 patients with undetectable HBV DNA levels, 19 (29.7%) patients demonstrated evidence of relapse. All the relapses occurred within 96 weeks after discontinuation. The median duration of relapse was 36 weeks (IQR: 12-48 weeks). Elevation of HBV DNA and ALT levels over baseline was only observed in 10% of the relapse patients. There were no significant differences among the baseline characteristics (sex, HBV genotype, age, or ALT level) or the time until consolidation therapy between relapse and sustained-response patients.
Conclusions:
NUC discontinuation is feasible after achieving undetectable HBV DNA levels in HBeAg-negative CHB patients. Prolonging the time until consolidation therapy may be a good strategy to decrease the rate of relapse. More than 96 weeks of sustained response is a predictive marker of long-term sustained response.
More Related Videos
Related Concept Videos
Hepatitis
Retrovirus Life Cycles
Inhibitors of Viral Protein Synthesis
Hepatic Drug Excretion: Enterohepatic Cycling
Post-release drugs and metabolites can be reabsorbed into the body from the intestine. For conjugated metabolites like glucuronides, reabsorption requires enzymatic hydrolysis by intestinal microflora. This...
Viral Hepatitis I: Introduction
Viruses with RNA Genomes

