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Antigen Targeting to Human HLA Class II Molecules Increases Efficacy of DNA Vaccination.

Journal of immunology (Baltimore, Md. : 1950) (2016-09-28)
Gunnveig Grodeland, Agnete Brunsvik Fredriksen, Geir Åge Løset, Elisabeth Vikse, Lars Fugger, Bjarne Bogen
RESUMEN

It has been difficult to translate promising results from DNA vaccination in mice to larger animals and humans. Previously, DNA vaccines encoding proteins that target Ag to MHC class II (MHC-II) molecules on APCs have been shown to induce rapid, enhanced, and long-lasting Ag-specific Ab titers in mice. In this study, we describe two novel DNA vaccines that as proteins target HLA class II (HLA-II) molecules. These vaccine proteins cross-react with MHC-II molecules in several species of larger mammals. When tested in ferrets and pigs, a single DNA delivery with low doses of the HLA-II-targeted vaccines resulted in rapid and increased Ab responses. Importantly, painless intradermal jet delivery of DNA was as effective as delivery by needle injection followed by electroporation. As an indication that the vaccines could also be useful for human application, HLA-II-targeted vaccine proteins were found to increase human CD4+ T cell responses by a factor of ×103 in vitro. Thus, targeting of Ag to MHC-II molecules may represent an attractive strategy for increasing efficacy of DNA vaccines in larger animals and humans.

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Sigma-Aldrich
Mouse Anti-Human IgG Antibody, clone HP6017, Fc, clone HP6017, Chemicon®, from mouse
Sigma-Aldrich
Anti-Mouse IgG (Fc specific)–Alkaline Phosphatase antibody produced in goat, affinity isolated antibody, buffered aqueous solution