Abstract
Tumor vaccines may induce activation and expansion of specific CD8 T cells which can subsequently destroy tumor cells in cancer patients. This phenomenon can be observed in approximately 5-20% of vaccinated melanoma patients. We searched for factors associated with T cell responsiveness to peptide vaccines. Peptide antigen-specific T cells were quantified and characterized ex vivo before and after vaccination. T cell responses occurred primarily in patients with T cells that were already pre-activated before vaccination. Thus, peptide vaccines can efficiently boost CD8 T cells that are pre-activated by endogenous tumor antigen. Our results identify a new state of T cell responsiveness and help to explain and predict tumor vaccine efficacy.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Adjuvants, Immunologic / therapeutic use
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Antibodies, Monoclonal / metabolism
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Antibody Specificity
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CD8-Positive T-Lymphocytes / immunology*
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CD8-Positive T-Lymphocytes / virology
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Cancer Vaccines / immunology*
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Cancer Vaccines / therapeutic use
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Epitopes / analysis
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Epitopes / immunology
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Epitopes / therapeutic use
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Fluorescent Dyes / metabolism
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Humans
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Influenza A virus / immunology
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Leukocytes, Mononuclear / immunology
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Leukocytes, Mononuclear / metabolism
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Lymphocyte Activation / immunology*
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Melanoma / immunology*
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Melanoma / therapy*
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Neoplasm Proteins / analysis
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Neoplasm Proteins / immunology
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Neoplasm Proteins / therapeutic use
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Peptide Fragments / analysis
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Peptide Fragments / immunology
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Peptide Fragments / therapeutic use
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Predictive Value of Tests
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Prognosis
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T-Lymphocyte Subsets / immunology*
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T-Lymphocyte Subsets / virology
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Viral Matrix Proteins / analysis
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Viral Matrix Proteins / immunology
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Viral Matrix Proteins / therapeutic use
Substances
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Adjuvants, Immunologic
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Antibodies, Monoclonal
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Cancer Vaccines
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Epitopes
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Fluorescent Dyes
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MART-1-Melan-A(27-35) epitope
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Neoplasm Proteins
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Peptide Fragments
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Viral Matrix Proteins
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influenza virus membrane protein (58-66)