Competition for antigen determines the stability of T cell-dendritic cell interactions during clonal expansion

Proc Natl Acad Sci U S A. 2007 Mar 13;104(11):4553-8. doi: 10.1073/pnas.0610019104. Epub 2007 Mar 2.

Abstract

The regulation of T cell-dendritic cell (DC) contacts during clonal expansion is poorly defined. Although optimal CD4 T cell responses require prolonged exposure to antigen (Ag), it is believed that stable T cell-DC interactions occur only during the first day of the activation process. Here we show that recently activated CD4 T cells are in fact fully competent for establishing contact with Ag-bearing DC. Using two-photon imaging, we found that whereas prolonged interactions between activated T cells and Ag-bearing DCs were infrequent at high T cell precursor frequency, they were readily observed for a period of at least 2 days when lower numbers of T cells were used. We provide evidence that, when present in high numbers, Ag-specific T cells still gained access to the DC surface but were competing for the limited number of sites on DCs with sufficient peptide-MHC complexes for the establishment of a long-lived interaction. Consistent with these findings, we showed that restoration of peptide-MHC level on DCs at late time points was sufficient to recover interactions between activated T cells and DCs. Thus, the period during which CD4 T cells continue to establish stable interactions with DCs is longer than previously thought, and its duration is dictated by both Ag levels and T cell numbers, providing a feedback mechanism for the termination of CD4 T cell responses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens / chemistry*
  • Binding, Competitive
  • CD4-Positive T-Lymphocytes / metabolism
  • Cell Communication
  • Cell Separation
  • Dendritic Cells / cytology*
  • Dendritic Cells / immunology
  • Dose-Response Relationship, Drug
  • Female
  • Flow Cytometry
  • Mice
  • Mice, Inbred C57BL
  • Peptides / chemistry
  • Photons
  • T-Lymphocytes / cytology*
  • T-Lymphocytes / immunology

Substances

  • Antigens
  • Peptides