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Expert Reviews in Molecular Medicine: http://www.expertreviews.org/
DOI: 10.1017/S1462399405010264; 20 December 2005
Beverley Wilkinson, Jocelyn S. Downey and Christopher E. Rudd (2005) T-cell signalling and immune system disorders.
Expert Rev. Mol. Med. Vol. 7, Issue 29, DOI: 10.1017/S1462399405010264

T-cell signalling and immune system disorders

Beverley Wilkinson, Jocelyn S. Downey and Christopher E. Rudd

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T-cell receptor (TCR) engagement initiates intracellular signalling cascades that lead to T-cell proliferation, cytokine production and differentiation into effector cells. These cascades comprise an array of protein-tyrosine kinases, phosphatases, GTP-binding proteins and adaptor proteins that regulate generic and specialised functions. The integration of these signals is essential for the normal development, homeostasis and function of T cells. Defects in a single mediator can produce T cells that are unable to participate fully in an immune response and/or that mount an inappropriate response, which leads to immunodeficiency, autoimmunity or leukaemia/lymphomas. This review highlights some of the key players in T-cell signalling and their involvement in the development of various clinical disease states. Some of these immune-specific signalling proteins are attractive potential targets in the development of therapies to augment T-cell responses to antigen or tumours, and to treat immune cell disorders.

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Figure 1. Receptors on T cells and their ligands on antigen-presenting cells.
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Figure 2. The T-cell signalling paradigm.
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Figure 3. Adaptors and molecular scaffolds in T-cell signalling.
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Figure 4. JAK–STAT and Smad signalling cascades.
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Figure 5. Immune disorders associated with T-cell signalling.
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Table 1. T-cell signalling proteins and human disease.
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