Journal article

Preclinical evaluation of therapeutic vaccines for chronic hepatitis B that stimulate antiviral activities of T cells and NKT cells

AH Mooney, SL Draper, OK Burn, RJ Anderson, BJ Compton, C Tang, KJ Farrand, P Di Lucia, M Ravà, V Fumagalli, L Giustini, E Bono, DI Godfrey, WR Heath, W Yuan, FV Chisari, LG Guidotti, M Iannacone, J Sidney, A Sette Show all

Jhep Reports | ELSEVIER | Published : 2024

Abstract

Background & Aims: Liver diseases resulting from chronic HBV infection are a significant cause of morbidity and mortality. Vaccines that elicit T-cell responses capable of controlling the virus represent a treatment strategy with potential for long-term effects. Here, we evaluated vaccines that induce the activity of type I natural killer T (NKT) cells to limit viral replication and license stimulation of conventional antiviral T-cells. Methods: Vaccines were prepared by conjugating peptide epitopes to an NKT-cell agonist to promote co-delivery to antigen-presenting cells, encouraging NKT-cell licensing and stimulation of T cells. Activity of the conjugate vaccines was assessed in transgenic..

View full abstract

University of Melbourne Researchers

Grants

Awarded by National Health and Medical Research Council


Funding Acknowledgements

This work was supported with funding from the New Zealand Ministry of Business Innovation and Employment (RTVU1603) , the Independent Research Organisation Fund of the Health Research Council of New Zealand to the Malaghan Institute (HRC14/10 03) , Callaghan Innovation R&D Project Grant (CONT-59888-PROJECT AIMMU) and Avalia Immunotherapies Limited. SAG was supported by Avalia Immunotherapies Limited. DIG was supported by an NHMRC SPRF fellowship (1117766) and now by an NHMRC Investigator grant (2008913) .