A novel vaccine adjuvant comprised of a synthetic innate defence regulator peptide and CpG oligonucleotide links innate and adaptive immunity |
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Authors: | Jason Kindrachuk,Hå vard Jenssen,Melissa Elliott,Rebecca Townsend,Anastasia Nijnik,Song F. Lee,Volker Gerdts,Lorne A. Babiuk,Scott A. Halperin,Robert E.W. Hancock |
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Affiliation: | 1. Centre for Microbial Diseases and Immunity Research, University of British Columbia, 2259 Lower Mall Research Station, Vancouver, BC, V6T 1Z3, Canada;2. Canadian Center for Vaccinology, Dalhousie University, IWK Health Centre, 5850/5980 University Avenue, Halifax, NS, B3K 6R8, Canada;3. Vaccine and Infectious Disease Organization, University of Saskatchewan, Saskatoon, SK, S7N 5E3, Canada;4. University of Alberta, 3-7 University Hall, Edmonton, AB, T6G 2J9, Canada |
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Abstract: | There has been an increased demand for the development of novel vaccine adjuvants that lead to enhanced induction of protection from infectious challenges and development of immunological memory. A novel vaccine adjuvant was developed comprising a complex containing CpG oligonucleotide and the synthetic cationic innate defence regulator peptide HH2 that has enhanced immune modulating activities. The complex of HH2 and the CpG oligonucleotide 10101 was a potent inducer of cytokine/chemokine expression ex vivo, retained activity following extended storage, had low associated cytotoxicity, and upregulated surface marker expression in dendritic cells, a critical activity for a vaccine adjuvant. Immunization of mice with a coformulation of the HH2–CpG complex and pertussis toxoid significantly enhanced the induction of toxoid-specific antibody titres when compared to toxoid alone, inducing high titres of IgG1 and IgG2a, typical of a balanced Th1/Th2 response, and also led to high IgA titres. |
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Keywords: | Adjuvant Innate defence regulator peptide Host defense peptide CpG DNA Oligodeoxynucleotides Toll-like receptors Formulation |
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