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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
Models for predicting hepatitis B e antigen seroconversion in response to interferon-α in chronic hepatitis B
Chang-Tai Wang1, Ya-Fei Zhang1, Bing-Hu Sun1
1Chang-Tai Wang, Ya-Fei Zhang, Bing-Hu Sun, Yu Dai, Hui-Lan Zhu, Xu Li, Zhen-Hua Zhang, Department of Infectious Diseases, the First Affiliated Hospital, Anhui Medical University, Hefei 230022, Anhui Province, China.
Predicting hepatitis B e antigen (HBeAg) seroconversion is possible with models developed from interferon (IFN)-α treatment data. These models identify key factors at baseline and during treatment to forecast patient response to IFN-α therapy for chronic hepatitis B.
Area of Science:
- Hepatology
- Virology
- Immunology
Background:
- Chronic hepatitis B (CHB) infection affects millions globally.
- Hepatitis B e antigen (HBeAg) seroconversion is a key indicator of treatment response.
- Interferon-alpha (IFN-α) is a treatment option for CHB.
Purpose of the Study:
- To develop predictive models for HBeAg seroconversion in CHB patients treated with IFN-α.
- To identify baseline and on-treatment predictors of response to IFN-α therapy.
Main Methods:
- 147 treatment-naïve HBeAg-positive CHB patients in China were analyzed.
- Serum biomarkers including ALT, HBV DNA, HBsAg, HBeAg, and anti-HBc were measured at multiple time points.
- Univariate and multivariate analyses were used to identify predictors and construct predictive models.
Main Results:
- Baseline predictors of seroconversion included high ALT, low HBeAg, and high anti-HBc levels.
- On-treatment predictors at 12 and 24 weeks included HBeAg levels, HBeAg decline, and anti-HBc levels.
- Models incorporating these factors showed significant differences in response rates based on predictive scores.
Conclusions:
- Predictive models with good positive and negative values were developed for IFN-α therapy response.
- These models can aid in calculating the probability of HBeAg seroconversion during IFN-α treatment.

