T-cell apoptosis in inflammatory brain lesions: destruction of T cells does not depend on antigen recognition

Am J Pathol. 1998 Sep;153(3):715-24. doi: 10.1016/s0002-9440(10)65615-5.

Abstract

Elimination of inflammatory T cells by apoptosis appears to play an important role in the down-regulation of inflammation in the central nervous system. Here we report that apoptosis of T lymphocytes occurs to a similar extent in different models of autoimmune encephalomyelitis. Apoptosis is restricted to cells located in the neuroectodermal parenchyma, thereby leaving T cells present in the brain's connective tissue compartments unharmed. Death of T cells in the parenchyma does not depend on antigen presentation by resident microglial cells or astrocytes. Adoptive transfer experiments with T lymphocytes carrying a specific genetic marker revealed that in the central nervous system these cells are destroyed regardless of their antigen specificity or state of activation. Although many of both antigen-dependent and -independent mechanisms in the induction of T-cell apoptosis may act simultaneously, our results suggest that the nervous system harbors a specific, currently undefined, mechanism that effectively eliminates infiltrating T lymphocytes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Antigen Presentation / immunology*
  • Apoptosis / immunology*
  • Brain / immunology
  • Brain / pathology
  • Cell Count
  • Cell Death
  • Cell Movement / immunology
  • Encephalomyelitis, Autoimmune, Experimental / immunology*
  • Encephalomyelitis, Autoimmune, Experimental / pathology
  • Immunoenzyme Techniques
  • Myelin Basic Protein / immunology
  • Rats
  • Rats, Inbred Lew
  • Spinal Cord / immunology
  • Spinal Cord / pathology
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / pathology

Substances

  • Myelin Basic Protein