Poster Presentation Asia-Pacific Vaccine and Immunotherapy Congress 2026

Therapeutic HBV vaccine efficacy through ancestral mismatched T cell epitopes (#108)

Akshay Binayke 1 , Nina Le Bert 1 , Shubhankar Ambike 1 , Shou Kit Hang 2 , Yazhini Avaiarasi 1 , Previtha D Sakthi Vale 1 , Natalene YH Shan 1 , Nicole Tan 1 , Adeline Chia 1 , Anthony Tanoto Tan 1 , Ying Tan 3 , Yun Ji 4 , Qing Zhu 4 , Antonio Bertoletti 1
  1. Duke-NUS Medical School, Singapore
  2. T Cell Diagnostics Pte Ltd, Singapore
  3. Brii Biosciences Inc, Beijing, China
  4. Brii Biosciences Inc, Durham, USA

Therapeutic vaccines for the treatment of chronic viral infections, such as HBV, have been mainly designed to target conserved viral regions and to preferentially restore dysfunctional virus-specific CD8 T cells. Such vaccines have failed to deliver clinical benefit, but a recent trial combining siRNA and peg-IFNα reported a remarkable ~50% HBsAg loss rate in chronic HBV patients who responded to the therapeutic vaccine BRII-179 administered prior to the trial. To define the underlying immunological mechanisms leading to the increased HBsAg loss rate, we longitudinally characterized vaccine-induced T and B cell responses using functional assays, persistence tracking, epitope mapping, phenotyping, and analysis of vaccine and infecting HBV sequences.

We found that BRII-179-mediated modulation of HBV-specific immunity did not result from recovery of pre-existing dysfunctional T cells. Instead, the vaccine primed novel IL-2-producing CD4⁺ T cells targeting epitopes that were largely mismatched to patients’ infecting HBV strains. These responses were driven by a PreS1 N-terminal domain sequence within the vaccine’s large S protein that shows high homology to HBV genotype G—a rare genotype thought to represent a remnant of an extinct prehistoric HBV lineage.

These vaccine-induced CD4⁺ T cells were detected in most vaccinated patients across diverse HLA class II backgrounds and persisted with stable functionality for more than two years. Despite their lack of cross-reactivity with contemporary HBV genotypes, the presence of these epitope-mismatched CD4⁺ T cells was associated with marked, progressive maturation of HBs-specific B cells during peg-IFNα/siRNA treatment, consistent with intermolecular T cell help.

We conclude that the ability of BRII-179 to increase HBsAg loss arises from the expansion of epitope-mismatched CD4⁺ T cells that promote HBs-specific B cell maturation during peg-IFNα treatment. These findings challenge current therapeutic vaccine strategies focused on conserved viral regions and CD8⁺ T cell responses and suggest that ancestral HBV epitopes lost during viral evolution may represent potent targets for inducing therapeutically effective antiviral immunity.