Abstract
Many tumors express tumor-specific antigens capable of being presented to CD8+ T cells by major histocompatibility complex (MHC) class I molecules. Antigen presentation models predict that the tumor cell itself should present these antigens to T cells. However, when conditions for the priming of tumor-specific responses were examined in mice, no detectable presentation of MHC class I-restricted tumor antigens by the tumor itself was found. Rather, tumor antigens were exclusively presented by host bone marrow-derived cells. Thus, MHC class I-restricted antigens are efficiently transferred in vivo to bone marrow-derived antigen-presenting cells, which suggests that human leukocyte antigen matching may be less critical in the application of tumor vaccines than previously thought.
MeSH terms
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Animals
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Antigen-Presenting Cells / immunology*
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Antigens, Neoplasm / immunology*
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Bone Marrow / immunology
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Bone Marrow Cells
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Colonic Neoplasms / immunology
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Epitopes
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Female
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Granulocyte-Macrophage Colony-Stimulating Factor / genetics
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Granulocyte-Macrophage Colony-Stimulating Factor / immunology
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H-2 Antigens / immunology
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Histocompatibility Antigens Class I / immunology*
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Melanoma, Experimental / immunology
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Mice
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Mice, Inbred BALB C
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Mice, Inbred C57BL
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Nucleocapsid Proteins
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Nucleoproteins*
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T-Lymphocytes, Cytotoxic / immunology*
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Tumor Cells, Cultured
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Viral Core Proteins / immunology
Substances
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Antigens, Neoplasm
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Epitopes
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H-2 Antigens
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Histocompatibility Antigens Class I
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Nucleocapsid Proteins
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Nucleoproteins
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Viral Core Proteins
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Granulocyte-Macrophage Colony-Stimulating Factor