Selective antigen presenting activity of cortical thymic epithelial cells against CD4+ T cells associated with both lack of costimulatory molecules and inefficient presentation of MHC-peptide ligands

Cell Immunol. 1997 Nov 1;181(2):163-71. doi: 10.1006/cimm.1997.1192.

Abstract

Selective activation among several effector functions of a T cell clone, DB14, specific for pigeon cytochrome c 43-58 (p43-58) and restricted to I-Ab/d was induced by antigen (Ag) presentation with nonprofessional Ag-presenting cells (APC), cortical thymic epithelial cells (c-TEC) (B7-1- CD40-), whereas full activation of the DB14 was induced with another nonprofessional APC, I-Ab L cell (B7-1+ CD40+). In the present study, to elucidate the mechanism underlying the selective activation of DB14 cells by c-TEC, we established c-TEC transfected with human CD40 alone (huCD40-c-TEC) or both human CD40 and murine B7-1 (huCD40/mB7-1-c-TEC), and compared the APC functions with those of the original c-TEC and I-Ab L cell. IFN-gamma production but not the proliferative response of DB14 was elevated by Ag presentation with huCD40-c-TEC as compared with unmanipulated c-TEC. On the other hand, upon stimulation with Ag plus huCD40/mB7-1-c-TEC both a significant proliferative response and IFN-gamma production were induced in DB14. However, the level of these responses did not reach that induced in the presence of I-Ab L cell. A similar pattern of APC functions was demonstrated with the other B7-independent T cell clone, PAB3, or T cell hybridomas (DBhy22 and BD7-5) which are basically independent of costimulation for the activation. The present finding along with our previous report that several structural differences of I-Ab molecules are present between c-TEC and I-Ab L cell suggests that the distinct APC activity of c-TEC is attributable not only to a lack of B7-1 and CD40 but also to inefficient presentation of MHC-peptide complex on the c-TEC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigen Presentation*
  • Apoptosis / immunology
  • B7-1 Antigen / genetics
  • B7-1 Antigen / physiology*
  • CD4-Positive T-Lymphocytes / immunology*
  • CD40 Antigens / genetics
  • CD40 Antigens / physiology*
  • Clone Cells / immunology
  • Cytotoxicity, Immunologic
  • Epithelial Cells / immunology
  • Histocompatibility Antigens Class II / immunology*
  • Humans
  • Hybridomas / immunology
  • Interferon-gamma / metabolism
  • Interleukin-2 / metabolism
  • Isoantigens / immunology
  • L Cells
  • Lymphocyte Activation
  • Mice
  • Recombinant Proteins / immunology
  • Thymus Gland / cytology*
  • Thymus Gland / immunology
  • Transfection

Substances

  • B7-1 Antigen
  • CD40 Antigens
  • Histocompatibility Antigens Class II
  • Interleukin-2
  • Isoantigens
  • Recombinant Proteins
  • Interferon-gamma