Abstract
Self-adjuvanting antitumor vaccines by multifunctional cationic nanohydrogels loaded with CpG. A conjugate consisting of tumor-associated MUC1-glycopeptide B-cell epitope and tetanus toxin T-cell epitope P2 is linked to cationic nanogels. Oligonucleotide CpG complexation enhances toll-like receptor (TLR) stimulated T-cell proliferation and rapid immune activation. This co-delivery promotes induction of specific MUC1-antibodies binding to human breast tumor cells without external adjuvant.
Keywords:
CpG codelivery; MUC1 glycopeptide; anti-tumor vaccines; cationic nanohydrogels; self-adjuvanting vaccines.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adjuvants, Immunologic / pharmacology*
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Amino Acid Sequence
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Animals
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Cancer Vaccines / immunology*
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Cations
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Enzyme-Linked Immunosorbent Assay
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Glycopeptides / chemistry
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Glycopeptides / immunology*
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Humans
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Hydrogel, Polyethylene Glycol Dimethacrylate / chemical synthesis
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Hydrogel, Polyethylene Glycol Dimethacrylate / chemistry*
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Mice, Inbred BALB C
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Molecular Sequence Data
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Nanoparticles / chemistry*
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Nanoparticles / ultrastructure
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Oligodeoxyribonucleotides / chemistry*
Substances
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Adjuvants, Immunologic
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CPG-oligonucleotide
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Cancer Vaccines
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Cations
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Glycopeptides
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Oligodeoxyribonucleotides
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Hydrogel, Polyethylene Glycol Dimethacrylate