Intradermal DNA electroporation induces survivin-specific CTLs, suppresses angiogenesis and confers protection against mouse melanoma
Author
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Lladser, Álvaro
Author
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Ljungberg, Karl
Author
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Tufvesson, Helena
Author
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Tazzari, Marcella
Author
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Roos, Anna Karin
Author
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Quest, Andrew F. G.
Author
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Kiessling, Rolf
Admission date
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2019-03-11T12:58:18Z
Available date
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2019-03-11T12:58:18Z
Publication date
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2010
Cita de ítem
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Cancer Immunology, Immunotherapy, Volumen 59, Issue 1, 2018, Pages 81-92
Identifier
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03407004
Identifier
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14320851
Identifier
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10.1007/s00262-009-0725-4
Identifier
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https://repositorio.uchile.cl/handle/2250/164865
Abstract
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Survivin is an intracellular tumor-associated antigen that is broadly expressed in a large variety of tumors and also in tumor associated endothelial cells but mostly absent in differentiated tissues. Naked DNA vaccines targeting survivin have been shown to induce T cell as well as humoral immune responses in mice. However, the lack of epitope-specific CD8+ T cell detection and modest tumor protection observed highlight the need for further improvements to develop effective survivin DNA vaccination approaches. Here, the efficacy of a human survivin DNA vaccine delivered by intradermal electroporation (EP) was tested. The CD8+ T cell epitope surv20-28 restricted to H-2 Db was identified based on in-silico epitope prediction algorithms and binding to MHC class I molecules. Intradermal DNA EP of mice with a human survivin encoding plasmid generated CD8+ cytotoxic T lymphocyte (CTL) responses cross-reactive with the mouse epitope surv20-28, as determined by intracellular IFN-γ staining, su