Journal article
Development of virus-like particles with inbuilt immunostimulatory properties as vaccine candidates
S Collett, L Earnest, J Carrera Montoya, MA Edeling, A Yap, CY Wong, D Christiansen, J Roberts, J Mumford, V Lecouturier, V Pavot, S Marco, JK Loi, C Simmons, SA Gulab, JM Mackenzie, A Elbourne, PA Ramsland, G Cameron, D Hans Show all
Frontiers in Microbiology | FRONTIERS MEDIA SA | Published : 2023
Abstract
The development of virus-like particle (VLP) based vaccines for human papillomavirus, hepatitis B and hepatitis E viruses represented a breakthrough in vaccine development. However, for dengue and COVID-19, technical complications, such as an incomplete understanding of the requirements for protective immunity, but also limitations in processes to manufacture VLP vaccines for enveloped viruses to large scale, have hampered VLP vaccine development. Selecting the right adjuvant is also an important consideration to ensure that a VLP vaccine induces protective antibody and T cell responses. For diseases like COVID-19 and dengue fever caused by RNA viruses that exist as families of viral variant..
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Grants
Awarded by National Health and Medical Research Council
Funding Acknowledgements
This work was supported by a grant from NHMRC MRFF 2020 COVID-19 Vaccine Candidate Research, Australia (APP2013957) and an unrestricted research grant from Sanofi Pasteur. The research was performed in part at the RMIT Micro Nano Research Facility (MNRF) in the Victorian Node of the Australian National Fabrication Facility (ANFF). The Cypher ES AFM instrument was funded in part by grant LE170100096 from the Australian Research Council (ARC). SC was supported by a research training program stipend scholarship from the Australian Government, Department of Education and Training. AE acknowledges support from the Jack Brockhoff Foundation (JBF Grant number 4655-2019) and was supported by an Australian Research Council (ARC) Discovery Early Career Research Award (DECRA) (DE220100511). JT acknowledges support from the National Health and Medical Research Council of Australia (APP1181580). DG was supported by an NHMRC Senior Principal Research Fellowship (1117766) and an NHMRC Investigator Award (2008913), and acknowledges support from the National Health and Medical Research Council of Australia (NHMRC; 1113293). JT and DG acknowledge support from the Jack Ma Foundation for parts of the SARS-CoV-2 VLP work in this manuscript.