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Updated: Mar 27, 2026

Reaggregate Thymus Cultures
Published on: August 28, 2008
The thymus and rheumatology: should we care?
Emilie Cosway1, Graham Anderson, Paul Garside
1aMRC Centre for Immunology, Institute for Immunology and Immunotherapy, Medical School, University of Birmingham, Birmingham bCentre for Immunobiology, Institute of Infection, Immunology and Inflammation, Glasgow Biomedical Research Centre, University of Glasgow, Glasgow, UK.
Purpose Of Review:
The purpose of this review is to discuss the mechanisms of central and peripheral tolerance in relation to T-cell mediated autoimmunity in rheumatoid arthritis (RA).
Recent Findings:
The well established association between major histocompatibility complex class II and RA has led us to understand that T cells, and the adaptive immune response, are important in the pathogenesis of disease. In order for autoimmune disease to develop, there is a breach of tolerance to self antigen and the mechanisms of both central and peripheral tolerance aim to prevent this. Here, we review evidence from mouse models indicating that alterations in T-cell receptor signalling thresholds during thymic selection may be linked to the escape of T cells that mediate autoimmune arthritis. In addition, we summarize the role of dendritic cells and Foxp3+ regulatory T cells in both peripheral and thymic tolerance, and highlight their relevance to what we know about the aetiology of RA.
Summary:
Mechanisms of central tolerance in the thymus and peripheral tolerance are in place to control autoreactive T cells and to prevent the development of autoimmune disease. We anticipate that a better understanding of these mechanisms will lead to the development of better, antigen-specific therapeutics to restore tolerance.
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