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

J Bauer, M Bradl, WF Hickey, S Forss-Petter… - The American journal of …, 1998 - Elsevier
J Bauer, M Bradl, WF Hickey, S Forss-Petter, H Breitschopf, C Linington, H Wekerle…
The American journal of pathology, 1998Elsevier
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 …
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.
Elsevier