The expansion of a CD4+ T cell population bearing a distinctive beta chain in MRL lpr/lpr mice suggests a role for the fas protein in peripheral T cell selection

Eur J Immunol. 1994 Nov;24(11):2761-6. doi: 10.1002/eji.1830241128.

Abstract

MRL lpr/lpr mice suffer from a systemic lupus erythematosus-like autoimmune disease. The lpr mutation impairs the normal transcription of the fas message, the product of which mediates apoptosis and presumably the proper selection of T cells. We have found an early expansion of CD4+ T cells bearing a distinctive V beta 8.3-D beta 1.1-J beta 1.1 T cell receptor beta chain in the periphery of MRL lpr/lpr mice, which was not detected in MRL +/+ mice nor in the thymus of MRL lpr/lpr mice. Thus, since thymic selection is normal in MRL lpr/lpr mice, we propose that the lpr mutation results in defective negative selection at the periphery.

MeSH terms

  • Animals
  • Antigens, Surface / physiology*
  • Base Sequence
  • CD4-Positive T-Lymphocytes / immunology*
  • Lupus Erythematosus, Systemic / immunology*
  • Mice
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • Receptors, Antigen, T-Cell, alpha-beta / analysis*
  • Receptors, Antigen, T-Cell, alpha-beta / genetics
  • fas Receptor

Substances

  • Antigens, Surface
  • Receptors, Antigen, T-Cell, alpha-beta
  • fas Receptor