Abstract
The use of a cell-based vaccine composed of autologous whole blood cells loaded with mRNA is described. Mice immunized with whole blood cells loaded with mRNA encoding antigen develop anti-tumor immunity comparable to DC-RNA immunization. This approach offers a simple and affordable alternative to RNA-based cellular therapy by circumventing complex, laborious and expensive ex vivo manipulations required for DC-based immunizations.
Keywords:
blood; cancer; immunotherapy; messenger RNA; vaccine.
© 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Animals
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Antigens, Neoplasm / genetics
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Antigens, Neoplasm / immunology
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Antigens, Neoplasm / metabolism
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Blood Cells / cytology
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Blood Cells / metabolism*
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Blood Cells / transplantation
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Cancer Vaccines / genetics
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Cancer Vaccines / immunology*
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Cancer Vaccines / metabolism
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Dendritic Cells / cytology
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Dendritic Cells / metabolism
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Dendritic Cells / transplantation
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Disease Models, Animal
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Electroporation
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Female
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Immunotherapy
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Intramolecular Oxidoreductases / genetics
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Intramolecular Oxidoreductases / metabolism
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Melanoma, Experimental / mortality
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Melanoma, Experimental / pathology
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Melanoma, Experimental / therapy
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Mice
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Mice, Inbred C57BL
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RNA, Messenger / chemistry
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RNA, Messenger / metabolism*
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Survival Rate
Substances
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Antigens, Neoplasm
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Cancer Vaccines
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RNA, Messenger
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Intramolecular Oxidoreductases
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dopachrome isomerase