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Antigen-Dependent Release of IFN-γ by Cytotoxic T Cells Up- Regulates Fas on Target Cells and Facilitates Exocytosis- Independent Specific Target Cell Lysis

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Tran,  Thao
Department of Cellular Immunology, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

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Stehle,  Thomas
Metchnikoff Laboratory, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

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Simon,  Markus M.
Metchnikoff Laboratory, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

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Citation

Müllbacher, A., Lobigs, M., Hla, R. T., Tran, T., Stehle, T., & Simon, M. M. (2002). Antigen-Dependent Release of IFN-γ by Cytotoxic T Cells Up- Regulates Fas on Target Cells and Facilitates Exocytosis- Independent Specific Target Cell Lysis. Journal of Immunology, 169(1), 145-150.


Cite as: https://hdl.handle.net/11858/00-001M-0000-002B-9628-C
Abstract
Effector cytolytic T (Tc) lymphocytes, deficient in the exocytosis-mediated pathway of target cell lysis, induce Fas on target cells and, in turn, delayed cell death and apoptosis via the Fas ligand-Fas interaction. The induction of Fas can be blocked by anti IFN-γ Abs. This Fas up-regulation on initially Fas-negative target cells is not mediated by TCR-MHC/peptide signaling per se, but by secreted IFN-γ from Tc cells after Ag engagement. The Fas up-regulation by Tc cells can be mimicked by treatment of target cells with rIFN-γ. Tc cells from IFN-γ knockout mice do not induce Fas expression on target cells. Te cell-mediated Fas expression on third party, bystander, target cells does not enhance their susceptibility to lysis by these nominal effector cells. The results are discussed as to the possible relevance of the phenomenon in efficiency and regulation of the Tc cell response to infections by viruses.