Regulatory T cells in rheumatoid arthritis: functions, development, regulation, and therapeutic potential

被引:0
作者
Shuaifeng Yan
Konstantin Kotschenreuther
Shuya Deng
David M. Kofler
机构
[1] University of Cologne,Laboratory of Molecular Immunology, Division of Rheumatology and Clinical Immunology, Department I of Internal Medicine, Faculty of Medicine and University Hospital Cologne
[2] University of Cologne,Center for Molecular Medicine Cologne (CMMC)
[3] University of Cologne,Department of Ophthalmology
[4] Aachen Bonn Cologne Duesseldorf,Center for Integrated Oncology
来源
Cellular and Molecular Life Sciences | 2022年 / 79卷
关键词
Regulatory T cells; Chimeric antigen receptor; CD4+ T cells; Therapeutic potential; Self-tolerance; Autoimmunity;
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摘要
Rheumatoid arthritis (RA) is an autoimmune disease that mainly affects the joints but also leads to systemic inflammation. Auto-reactivity and dysregulation of self-tolerance are thought to play a vital role in disease onset. In the pathogenesis of autoimmune diseases, disturbed immunosuppressive properties of regulatory T cells contribute to the dysregulation of immune homeostasis. In RA patients, the functions of Treg cells and their frequency are reduced. Therefore, focusing on the re-establishment of self-tolerance by increasing Treg cell frequencies and preventing a loss of function is a promising strategy for the treatment of RA. This approach could be especially beneficial for those patients who do not respond well to current therapies. In this review, we summarize and discuss the current knowledge about the function, differentiation and regulation of Treg cells in RA patients and in animal models of autoimmune arthritis. In addition, we highlight the therapeutic potential as well as the challenges of Treg cell targeting treatment strategies.
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