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      Induction of apoptosis in mature T cells by tumour necrosis factor.

      Nature
      Mice, Inbred C57BL, Animals, Apoptosis, Cell Line, Fas Ligand Protein, Membrane Glycoproteins, deficiency, physiology, Mice, Mice, Inbred C3H, Receptors, Antigen, T-Cell, Receptors, Tumor Necrosis Factor, T-Lymphocytes, Tumor Necrosis Factor-alpha

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          Abstract

          T-cell receptor-induced apoptosis regulates immune responses and can result from interactions between Fas (Apo1/CD95) and Fas ligand (FasL). Mutations in the genes for Fas and FasL cause disorders resembling human autoimmune diseases in lpr and gld mice, respectively. However, peripheral T-cell deletion takes place in lpr mice, and autoimmune syndromes occur in mouse strains without Fas or FasL defects. Here we show that tumour necrosis factor (TNF) can mediate mature T-cell receptor-induced apoptosis through the p75 TNF receptor. Blockage of both TNF and FasL is required to abrogate T-cell death and TNF mediates the death of most CD8+ T cells, whereas FasL mediates the death of most CD4+ T cells. Our results suggest that autoregulatory apoptosis of the mature T cells can occur by two distinct molecular mechanisms.

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