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IP-10 Expression in Patients with Chronic HBV Infection and Its Ability to Predict the Decrease in HBsAg Levels after
Kai Zhao1, Tao Yang2, Mimi Sun3
1Institute of Immunology, Taishan Medical University, Tai'an 271000, China.
Molecules and Cells
|June 16, 2017
Summary
Baseline levels of Interferon-γ-inducible protein 10 (IP-10) predict treatment response in chronic hepatitis B (CHB) patients receiving entecavir. Higher IP-10 indicates better outcomes and reduced hepatitis B surface antigen levels.
Area of Science:
- Hepatology
- Immunology
- Virology
Background:
- Interferon-γ-inducible protein 10 (IP-10), or CXCL10, is linked to antiviral immunity and chronic hepatitis B (CHB) progression.
- The predictive value of baseline IP-10 for nucleoside/nucleotide analogue (NA) treatment efficacy in CHB remains unclear.
Purpose of the Study:
- To investigate the utility of baseline serum and intrahepatic IP-10 levels in predicting the efficacy of entecavir (ETV) therapy in CHB patients.
- To explore the association between IP-10 expression and liver inflammation, fibrosis, and hepatitis B virus (HBV) markers.
Main Methods:
- Systematic examination of intrahepatic and peripheral IP-10 levels before and after ETV treatment.
- Correlation analysis of baseline IP-10 with clinical parameters (ALT, AST, HBV DNA, HBsAg) and histological findings.
- In vitro experiments to assess IP-10's direct effect on hepatocyte apoptosis.
Main Results:
- Baseline IP-10 levels were elevated in CHB patients, correlating with increased liver inflammation and fibrosis.
- Higher baseline intrahepatic IP-10 predicted better prognoses and a greater decrease in HBsAg levels post-ETV therapy.
- Monocyte-derived IP-10 was higher in CHB patients compared to liver cirrhosis and healthy controls; IP-10 promoted hepatocyte apoptosis in vitro.
Conclusions:
- Baseline serological and histological IP-10 levels can predict CHB severity.
- IP-10 levels may serve as a biomarker for predicting the reduction of HBsAg during entecavir therapy.

