Characterization at the single-cell level of naive and primed CD8 T cell cytokine responses

Cell Immunol. 2000 Nov 25;206(1):16-25. doi: 10.1006/cimm.2000.1720.

Abstract

The aim of this study was to characterize differences between naive and primed CD8 T cells. Our results show that (i) naive and primed CD8 T cells display similar activation thresholds, with no direct evidence for a difference in their TCR signals, and (ii) primed cells differ mainly in their capacity to secrete IFN-gamma. A comparison of the two populations at the single-cell level demonstrated that the increased production of IFN-gamma by the primed cell subset is due to a larger proportion of single cells that are able to synthesize this cytokine early following activation. These results indicate that the intrinsic effector capabilities of individual CD8 T cells expressing the same TCR are heterogeneous and that cells with identical antigen specificity but increased effector capacities are generated or selected during the primary response.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Viral / immunology
  • CD8 Antigens / immunology
  • CD8-Positive T-Lymphocytes / metabolism*
  • Calcium Signaling
  • Cells, Cultured
  • Flow Cytometry
  • Immunization
  • Immunologic Memory / immunology*
  • Influenza A virus / immunology
  • Interferon-gamma / biosynthesis
  • Interferon-gamma / metabolism*
  • Lymphocyte Activation*
  • Lymphokines / biosynthesis
  • Lymphokines / metabolism
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Phosphorylation
  • Protein Processing, Post-Translational
  • Protein-Tyrosine Kinases / metabolism
  • Receptor Cross-Talk
  • Receptors, Antigen, T-Cell / immunology*

Substances

  • Antigens, Viral
  • CD8 Antigens
  • Lymphokines
  • Receptors, Antigen, T-Cell
  • Interferon-gamma
  • Protein-Tyrosine Kinases