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pubmed-article:17113202pubmed:abstractTextAngiogenesis is a rate-limiting step in the development of tumors. Here, we demonstrate that oral minigene DNA vaccines against murine vascular endothelial growth factor receptor-2 (FLK-1), a self-antigen overexpressed on proliferating endothelial cells in the tumor vasculature, induced protection against tumors of different origin in syngeneic BALB/c mice. This protection is mediated by CD8 T cells, which specifically kill FLK-1(+) endothelial cells, resulting in marked suppression of tumor angiogenesis. More importantly, the minigene vaccine proved to be of similar efficacy as a vaccine encoding the whole FLK-1 gene. These data suggest a FLK-1 minigene vaccine provides a more flexible alternative to the whole gene vaccine and will facilitate their future design and clinical applications in cancer therapy and prevention.lld:pubmed
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pubmed-article:17113202pubmed:authorpubmed-author:ZhouHeHlld:pubmed
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pubmed-article:17113202pubmed:articleTitleFLK-1-based minigene vaccines induce T cell-mediated suppression of angiogenesis and tumor protective immunity in syngeneic BALB/c mice.lld:pubmed
pubmed-article:17113202pubmed:affiliationDepartment of Immunology, The Scripps Research Institute, R218, IMM13, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.lld:pubmed
pubmed-article:17113202pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:17113202pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
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