Tumor necrosis factor receptor p55 mediates deletion of peripheral cytotoxic T lymphocytes in vivo

DE Speiser, E Sebzda, T Ohteki… - European journal of …, 1996 - Wiley Online Library
DE Speiser, E Sebzda, T Ohteki, MF Bachmann, K Pfeffer, TW Mak, PS Ohashi
European journal of immunology, 1996Wiley Online Library
Cellular death of activated lymphocytes down‐regulates immune responses and is involved
in maintaining self tolerance. Signals associated with ligation of the membrane molecule
Fas lead to lymphocyte apoptosis, but additional, Fasindependent mechanisms have been
postulated. Here, we show a marked expansion and prolonged persistence of functional
activated cytotoxic T cells in mice lacking the tumor necrosis factor (TNF) receptor p55. In the
absence of this receptor, peripheral lymphocyte apoptosis was significantly reduced in vivo …
Abstract
Cellular death of activated lymphocytes down‐regulates immune responses and is involved in maintaining self tolerance. Signals associated with ligation of the membrane molecule Fas lead to lymphocyte apoptosis, but additional, Fasindependent mechanisms have been postulated. Here, we show a marked expansion and prolonged persistence of functional activated cytotoxic T cells in mice lacking the tumor necrosis factor (TNF) receptor p55. In the absence of this receptor, peripheral lymphocyte apoptosis was significantly reduced in vivo. The prolonged thymocyte survival was associated with functional anergy, since the T cells no longer proliferated in vitro when stimulated with peptide antigen. However, specific cytotoxic effector function was easily detected in vitro. We conclude that the TNF receptor p55 is involved in peripheral T cell deletion in vivo.
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