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      Multiple functions for CD28 and cytotoxic T lymphocyte antigen-4 during different phases of T cell responses: implications for arthritis and autoimmune diseases

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          Abstract

          Chronic T cell responses, as they occur in rheumatoid arthritis, are complex and are likely to involve many mechanisms. There is a growing body of evidence that, in concert with the T cell antigen receptor signal, CD28 and cytotoxic T-lymphocyte antigen-4 (CTLA-4; CD152) are the primary regulators of T cell responses. Whereas CD28 primarily activates T cell processes, CTLA-4 inhibits them. The mechanism for this dichotomy is not fully understood, especially as CD28 and CTLA-4 recruit similar signalling molecules. In addition, recent studies demonstrate that CD28 and CTLA-4 have multiple functions during T cell responses. In particular, CTLA-4 exerts independent distinct effects during different phases of T cell responses that could be exploited for the treatment of rheumatoid arthritis.

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          Most cited references87

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          Cellular survival: a play in three Akts.

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            Lymphoproliferation disorder in mice explained by defects in Fas antigen that mediates apoptosis.

            Fas antigen is a cell-surface protein that mediates apoptosis. It is expressed in various tissues including the thymus and has structural homology with a number of cell-surface receptors, including tumour necrosis factor receptor and nerve growth factor receptor. Mice carrying the lymphoproliferation (lpr) mutation have defects in the Fas antigen gene. The lpr mice develop lymphadenopathy and suffer from a systemic lupus erythematosus-like autoimmune disease, indicating an important role for Fas antigen in the negative selection of autoreactive T cells in the thymus.
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              Lymphoproliferative disorders with early lethality in mice deficient in Ctla-4.

              The role of the cell-surface molecule CTLA-4 in the regulation of T cell activation has been controversial. Here, lymph nodes and spleens of CTLA-4-deficient mice accumulated T cell blasts with up-regulated activation markers. These blast cells also infiltrated liver, heart, lung, and pancreas tissue, and amounts of serum immunoglobulin were elevated. The mice invariably became moribund by 3 to 4 weeks of age. Although CTLA-4-deficient T cells proliferated spontaneously and strongly when stimulated through the T cell receptor, they were sensitive to cell death induced by cross-linking of the Fas receptor and by gamma irradiation. Thus, CTLA-4 acts as a negative regulator of T cell activation and is vital for the control of lymphocyte homeostasis.
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                Author and article information

                Journal
                Arthritis Res Ther
                Arthritis Research & Therapy
                BioMed Central (London )
                1478-6354
                1478-6362
                2004
                3 March 2004
                : 6
                : 2
                : 45-54
                Affiliations
                [1 ]Molecular Immunology, Deutsches Rheuma-Forschungszentrum Berlin, Germany
                [2 ]Charité, Universitätsmedizin Berlin, Germany
                Article
                ar1158
                10.1186/ar1158
                400439
                15059264
                dc64ef14-e412-4940-b03c-9e94b1cbe268
                Copyright © 2004 BioMed Central Ltd
                History
                : 15 December 2003
                : 27 January 2004
                : 11 February 2004
                : 12 February 2004
                Categories
                Review

                Orthopedics
                inflammation,ctla-4ig,cd152,polymorphism,signal transduction,costimulation
                Orthopedics
                inflammation, ctla-4ig, cd152, polymorphism, signal transduction, costimulation

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