Journal article
Glycolipid-peptide vaccination induces liver-resident memory CD8 T cells that protect against rodent malaria
LE Holz, YC Chua, MN de Menezes, RJ Anderson, SL Draper, BJ Compton, STS Chan, J Mathew, J Li, L Kedzierski, Z Wang, L Beattie, MH Enders, S Ghilas, R May, TM Steiner, J Lange, D Fernandez-Ruiz, AM Valencia-Hernandez, TL Osmond Show all
Science Immunology | AMER ASSOC ADVANCEMENT SCIENCE | Published : 2020
Abstract
Liver resident-memory CD8+ T cells (TRM cells) can kill liver-stage Plasmodium-infected cells and prevent malaria, but simple vaccines for generating this important immune population are lacking. Here, we report the development of a fully synthetic self-adjuvanting glycolipid-peptide conjugate vaccine designed to efficiently induce liver TRM cells. Upon cleavage in vivo, the glycolipid-peptide conjugate vaccine releases an MHC I-restricted peptide epitope (to stimulate Plasmodium-specific CD8+ T cells) and an adjuvant component, the NKT cell agonist α-galactosylceramide (α-GalCer). A single dose of this vaccine in mice induced substantial numbers of intrahepatic malaria-specific CD8+ T cells..
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Grants
Awarded by Australian Research Council
Funding Acknowledgements
This work was supported by the Australian Research Council (CE140100011), National Health and Medical Research Council (NHMRC; 1113293), New Zealand Ministry of Business Innovation and Employment (RTVU1603), and Avalia Immunotherapies. K.K., D.I.G, and W.R.H. are NHMRC Senior Principal Research Fellows (1117766 and 1154457).