| Literature DB >> 29223787 |
José Herrera-Rodriguez1, Tjarko Meijerhof1, Hubert G Niesters1, Grete Stjernholm2, Arnt-Ove Hovden2, Birger Sørensen3, Mats Ökvist2, Maja A Sommerfelt2, Anke Huckriede4.
Abstract
Current influenza vaccines mainly induce antibody responses to the variable hemagglutinin proteins of the virus strains included in the vaccine. Instead, a broadly protective influenza vaccine should aim at inducing antibody- and/or cell-mediated immunity against conserved viral proteins. Vacc-FLU is a peptide based vaccine combining conserved B and T cell epitopes. Peptide selection was done using a proprietary peptide design platform technology focusing on responses to human leukocyte antigen (HLA)-restricted epitopes. Immunization of wild-type mice and mice transgenic for HLA-A2.1 with the peptide mix successfully induced both humoral and cell mediated immune responses. Partial protection from severe weight loss upon challenge was observed in both mouse strains but was stronger and observed at lower vaccine doses in transgenic mice. Our results show that the Vacc-FLU peptide mix is capable of inducing IFNγ-producing T cells and antibody-producing B cells which can protect from severe disease symptoms upon infection.Entities:
Keywords: Cell mediated immunity; Humoral immunity; Influenza; Peptides; Universal vaccine
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Year: 2017 PMID: 29223787 DOI: 10.1016/j.virol.2017.11.018
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616