Hepatitis B core–based virus–like particles to present heterologous epitopes
Authors:
- Sarah De BaetsSBSarah De Baets
- Bert SchepensBSBert Schepens
- Xavier SaelensXSXavier Saelens
- 1 February 2013
- journal article
- review article
- Published by Taylor & Francis in Expert Review of Vaccines
- Vol. 12 (2) , 183-198
Abstract
Since the first effort to recombinantly express the hepatitis B core protein (HBc) in bacteria, the remarkable virion-like structure has fuelled interest in unraveling the structural and antigenic properties of this protein. Initial studies proved HBc virus-like particles to possess strong immunogenic properties, which can be conveyed to linked antigens. More than 35 years later, numerous studies have been performed using HBc as a carrier protein for antigens derived from over a dozen different pathogens and diseases. In this review, the authors highlight the intriguing features of HBc as carrier and antigen, illustrated by some examples and experimental results that underscore the value of HBc as an antigen-presenting platform. Two of these HBc fusions, targeting influenza A and malaria, have even progressed into clinical testing. In the future, the HBc-based virus-like particles platform will probably continue to be used for the display of poorly immunogenic antigens, mainly because virus-like particle formation by HBc capsomers is compatible with nearly any available recombinant gene expression system.Keywords
This publication has 166 references indexed in Scilit:
- Delivery of woodchuck hepatitis virus-like particle presented influenza M2e by recombinant attenuated Salmonella displaying a delayed lysis phenotypeVaccine, 2010
- Influenza Virus M2 Protein Mediates ESCRT-Independent Membrane ScissionCell, 2010
- Matrix Protein 2 of Influenza A Virus Blocks Autophagosome Fusion with LysosomesCell Host & Microbe, 2009
- Multiepitope peptide-loaded virus-like particles as a vaccine against hepatitis B virus–related hepatocellular carcinoma #Hepatology, 2009
- Internal Core Protein Cleavage Leaves the Hepatitis B Virus Capsid Intact and Enhances Its Capacity for Surface Display of Heterologous Whole Chain ProteinsJournal of Biological Chemistry, 2008
- Development of a universal influenza A vaccine based on the M2e peptide fused to the papaya mosaic virus (PapMV) vaccine platformVaccine, 2008
- Advantages to the use of rodent hepadnavirus core proteins as vaccine platformsVaccine, 2007
- Characterization of a hepatitis B and hepatitis delta virus receptor binding site†Hepatology, 2006
- Determination of the fold of the core protein of hepatitis B virus by electron cryomicroscopyNature, 1997
- Myristylation of the Hepatitis B Virus Large Surface Protein Is Essential for Viral InfectivityVirology, 1995