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pubmed-article:12706680pubmed:abstractTextA carcinoembryonic antigen (CEA)-based DNA vaccine, adsorbed onto cationic microparticles of poly(DL-lactide-co-glycolide) (PLG) induced tumor-protective immunity against a lethal challenge of MC38-CEA colon carcinoma cells in CEA-transgenic mice that was more potent than that of the corresponding naked DNA vaccine. Boosting with a plasmid encoding murine GM-CSF increased the vaccine's efficacy leading to a complete rejection of tumor cells in 50% of mice. This effect was due to activation of MHC class I-restricted CD8(+) T cells coupled with an increased secretion of proinflammatory cytokines IFN-gamma, TNF-alpha and IL-2. Also, specific activation of dendritic cells was indicated by a two-three-fold upregulation of their costimulatory CD80 and MHC class II molecules. This approach may be a promising new strategy for the rational design of cancer vaccines for future clinical applications.lld:pubmed
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pubmed-article:12706680pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:12706680pubmed:articleTitlePlasmid DNA encoding human carcinoembryonic antigen (CEA) adsorbed onto cationic microparticles induces protective immunity against colon cancer in CEA-transgenic mice.lld:pubmed
pubmed-article:12706680pubmed:affiliationDepartment of Immunology, The Scripps Research Institute, 10550 North Torrey Pines Road, IMM13, La Jolla, CA 92037, USA.lld:pubmed
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