Journal article
Polymerisation of a T cell epitope with an immunostimulatory C3d peptide sequence enhances antigen specific T cell responses
NM O'Brien-Simpson, TJ Attard, B Zheng, KA Walsh, EC Reynolds
International Journal of Peptide Research and Therapeutics | SPRINGER | Published : 2013
Abstract
The complement protein C3d and C3d derived peptides that bind CD21 are known to enhance immunity to co-immunised antigens. In this study we have synthesised the minimal CD21 binding sequence of C3d (1227LYNVEA 1232) as mono, di and tri tandem repeats and derivatised the N-terminus with an acryloyl moiety. These acryloyl-(C3d) n peptides were co-polymerised with a acryloyl-T cell epitope (PAS1K) from the Porphyromonas gingivalis antigen the RgpA-Kgp proteinase-adhesin complex. The ability of C3d containing polymers to enhance T cell immunity in vitro and in vivo was evaluated. When used to stimulate in vitro PAS1K-primed or RgpA-Kgp complex-primed T cells the C3d containing PAS1K polymers ind..
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Grants
Awarded by National Health and Medical Research Council
Funding Acknowledgements
We also wish to thank Ms Jenny Davis for the animal welfare and handling. This work was supported by NHMRC Grants: APP1029878 and APP1008106.