Tracking B cell immunity during perturbation of hepatitis B infection induced by treatment withdrawal - Summary - MDSpire
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Monitoring B cell Immune Responses Following Discontinuation of Treatment in Hepatitis B Infection

  • By

  • Sabela Lens

  • Alice R Burton

  • Jessica Davies

  • Maelle Locatelli

  • Mireia García-López

  • Anna Pocurull

  • Anna Jeffery-Smith

  • Nikolai Novikov

  • Simon P Fletcher

  • Xavier Forns

  • Sofía Pérez-del-Pulgar

  • Mala K Maini

  • August 1, 2026

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Objective:

To investigate the changes in B cell immune responses following the discontinuation of nucleos(t)ide analogue (NA) therapy in patients with chronic hepatitis B (CHB).

Approach:
  • Patient Selection: 21 patients with HBeAg-negative CHB who had complete virological control for at least 3 years under NA therapy were included.
  • Study Design: Patients underwent liver biopsy before treatment withdrawal and had serum samples and PBMCs collected at baseline, 12 weeks, and 48 weeks after NA discontinuation.
  • Comparative Analysis: The study compared the frequencies and phenotypes of HBc and HBs-specific memory B cells (MBC) and activated circulating T follicular helper cells.
Key Findings:
  • Prolonged NA therapy equalizes frequencies of class-switched MBC specific for HBc and HBs.
  • PD-1 expression on HBs-MBC is reduced only after treatment withdrawal, with sustained reductions seen in those achieving HBsAg loss.
  • Increased activated MBC, plasmablasts, and functional potential of HBs-MBC are observed in patients with HBsAg loss.
Interpretation:

Limitations:
  • Small sample size of 21 patients may limit the generalizability of the findings.
  • The study only includes patients with HBeAg-negative CHB, which may not represent all CHB patients.
Conclusion:

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