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Updated: Apr 17, 2026

Development of a Hepatitis B Virus Reporter System to Monitor the Early Stages of the Replication Cycle
Published on: February 1, 2017
Transbody against hepatitis B virus core protein inhibits hepatitis B virus replication in vitro
Yawen Wang1, Yiping Li2, Na Li3
1Department of Laboratory Medicine, First Affiliated Hospital, School of Medicine, Xi'an Jiaotong University, Xi'an 710061, Shaanxi, China.
Insights
A novel transbody targeting Hepatitis B virus core antigen (HBcAg) effectively inhibits viral replication. This cell-permeable antibody shows potent antiviral activity, offering a promising new therapeutic strategy for Hepatitis B infection.
Area of Science:
- Hepatology
- Virology
- Immunology
Background:
- Hepatitis B virus (HBV) infection is a leading cause of chronic liver disease with limited therapeutic options.
- The HBV core antigen (HBcAg) plays critical roles in the viral life cycle, making it a potential therapeutic target.
Purpose of the Study:
- To develop and evaluate a novel transbody, a conjugate of a monoclonal antibody against HBcAg and a TAT protein transduction domain (TAT PTD).
- To assess the efficacy of this HBcMAb-TAT PTD transbody in inhibiting HBV replication in vitro.
Main Methods:
- Conjugation of a monoclonal antibody against HBcAg with TAT PTD to create a cell-penetrating transbody.
- Evaluation of the transbody's recognition of HBcAg and its cell-penetrating activity in living cells.
- Assessment of the transbody's effect on HBV replication markers (HBsAg, HBeAg, HBcAg, and HBV DNA) in HepG2.2.15 cells.
Main Results:
- The HBcMAb-TAT PTD transbody demonstrated effective cell-penetrating ability.
- The transbody significantly suppressed extracellular and intracellular HBV markers, including HBsAg, HBeAg, HBcAg, and HBV DNA.
- Antiviral activity was observed in a dose-dependent manner.
Conclusions:
- The developed transbody is cell-permeable and exhibits potent anti-HBV replication activity.
- This HBcAg-targeting, cell-permeable antibody represents a novel therapeutic approach for Hepatitis B infection.
- Blocking HBcAg functions via this transbody strategy shows promise for controlling HBV.
Abstract:
Hepatitis B virus (HBV) infection is one of the major causes of chronic liver diseases. The current therapeutics show limited efficacy. In the HBV life cycle, virus core antigen (HBcAg) plays important multiple roles. Blocking the pleiotropic functions of HBcAg may thus represent a promising strategy for anti-HBV replication. In this study, monoclonal antibody (MAb) against core antigen of human HBV was coupled with TAT protein transduction domain (TAT PTD) to form transbody, and the effect on virus replication was evaluated in vitro. The HBV transbody, HBcMAb-TAT PTD conjugate, recognized HBcAg and retained cell-penetrating activity in living cells. In HBV-transfected liver cell line HepG2.2.15, HBV transbody suppressed not only the extracellular HBsAg, HBeAg and HBV DNA, but also the intracellular HBsAg, HBeAg, HBcAg and HBV DNA in a dose-dependent manner. These results indicate that the transbody prepared possesses readily cell-penetrating ability and potent antiviral activity, providing a novel approach, a cell-permeable antibody against HBcAg, for the treatment of HBV infection.
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