Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

TRAIL (tumor necrosis factor-related apoptosis-inducing ligand) is a recently identified member of the tumor necrosis factor cytokine superfamily. TRAIL has been shown to induce apoptosis in various tumor cell lines, whereas most primary cells seem to be resistant. These observations have raised considerable interest in the use of TRAIL in tumor therapy. Yet little is known about the physiological function of TRAIL. This is particularly the case in the immune system, where TRAIL has been suggested by some to be involved in target cell killing and lymphocyte death. We have developed a panel of mAbs and soluble proteins to address the role of TRAIL in lymphocyte development. These studies demonstrate activation-induced sensitization of thymocytes to TRAIL-mediated apoptosis and expression of the apoptosis-inducing TRAIL receptors. However, with the use of several model systems, our subsequent experiments rule out the possibility that TRAIL plays a major role in antigen-induced deletion of thymocytes. In contrast to thymocytes, there is no up-regulation of TRAIL receptors in peripheral T cells on activation, which remain resistant to TRAIL. Thus, susceptibility to TRAIL-induced apoptosis is controlled differently by central and peripheral T cells.

Type

Journal article

Journal

Proceedings of the National Academy of Sciences of the United States of America

Publication Date

17/04/2001

Volume

98

Pages

5158 - 5163

Addresses

Medical Research Council Human Immunology Unit, Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford OX3 9DS, United Kingdom. katja.simon@ndm.ox.ac.uk

Keywords

Thymus Gland, T-Lymphocytes, Cells, Cultured, Jurkat Cells, Animals, Mice, Knockout, Humans, Mice, Tumor Necrosis Factor-alpha, ATP-Binding Cassette Transporters, Membrane Glycoproteins, Receptors, Tumor Necrosis Factor, Antigens, CD4, Antigens, CD8, Antibodies, Monoclonal, Flow Cytometry, Organ Culture Techniques, Lymphocyte Activation, Apoptosis, Cytotoxicity, Immunologic, Clonal Deletion, Genes, RAG-1, Child, Preschool, Infant, Apoptosis Regulatory Proteins, TNF-Related Apoptosis-Inducing Ligand, Receptors, TNF-Related Apoptosis-Inducing Ligand