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      Kinetics of TCR use in response to repeated epitope-specific immunization.

      The Journal of Immunology Author Choice
      Cancer Vaccines, administration & dosage, immunology, Clone Cells, Dose-Response Relationship, Immunologic, Down-Regulation, Epitopes, T-Lymphocyte, metabolism, HLA Antigens, analysis, Humans, Immunization Schedule, Kinetics, Ligands, Lymphocyte Activation, Lymphocyte Count, Melanoma, Membrane Glycoproteins, Neoplasm Proteins, Peptide Fragments, Peptides, Protein Binding, Receptors, Antigen, T-Cell, Stem Cells, pathology, T-Lymphocytes, Tumor Cells, Cultured, gp100 Melanoma Antigen

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          Abstract

          Selection of T cell-directed immunization strategies is based extensively on discordant information derived from preclinical models. We characterized the kinetics of T cell selection in response to repeated antigenic challenge. By enumerating with epitope/HLA tetrameric complexes (tHLA) vaccine-elicited T cell precursor frequencies (Tc-pf) in melanoma patients exposed to the modified gp100 epitope gp100:209-217 (g209-2M) we observed in most patients that the Tc-pf increased with number of immunizations. One patient's kinetics were further characterized. Dissociation kinetics of g209-2M/tHLA suggested enrichment of T cell effector populations expressing TCR with progressively higher affinity. Furthermore, vaccine-elicited T cells maintained the ability to express IFN-gamma ex vivo and proliferate in vitro. Thus, repeated exposure to immunogenic peptides benefited immune competence. These results provide a rationale for immunization strategies.

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