Engineered antigen-specific regulatory T cells for autoimmune skin conditions

免疫学 免疫系统 周边公差 医学 白癜风 类天疱疮 免疫耐受 T细胞受体 抗原 调节性T细胞 T细胞 自身免疫 白细胞介素2受体 抗体 大疱性类天疱疮
作者
Zhussipbek Mukhatayev,Yekaterina O. Ostapchuk,Deyu Fang,I. Caroline Le Poole
出处
期刊:Autoimmunity Reviews [Elsevier]
卷期号:20 (3): 102761-102761 被引量:42
标识
DOI:10.1016/j.autrev.2021.102761
摘要

Regulatory T cells (Tregs) are a subset of T cells responsible for the regulation of immune responses, thereby maintaining immune homeostasis and providing immune tolerance to both self and non-self-antigens. An increasing number of studies revealed Treg numbers and functions in a variety of autoimmune diseases. Treg deficiency can cause the development of several autoimmune skin diseases including vitiligo, alopecia areata, pemphigoid and pemphigus, psoriasis, and systemic sclerosis. Many clinical trials have been performed for autoimmune conditions using polyclonal Tregs, but efficiency can be significantly improved using antigen-specific Tregs engineered using T cell receptor (TCR) or chimeric antigen receptor (CAR) constructs. In this review, we systematically reviewed altered frequencies, impaired functions, and phenotypic features of Tregs in autoimmune skin conditions. We also summarized new advances in TCR and CAR based antigen-specific Tregs tested both in animal models and in clinics. The advantages and limitations of each approach were carefully discussed emphasizing possible clinical relevance to patients with autoimmune skin diseases. Moreover, we have reviewed potential approaches for engineering antigen-specific Tregs, and strategies for overcoming possible hurdles in clinical applications. Thereby, antigen-specific Tregs can be infused using autologous adoptive cell transfer to restore Treg numbers and to provide local immune tolerance for autoimmune skin disorders.
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