Lan Ruth Y, Ansari Aftab A, Lian Zhe-Xiong, Gershwin M Eric
Division of Rheumatology, Allergy and Clinical Immunology, University of California at Davis, TB 192, One Shields Avenue, Davis, CA 95616, USA.
Autoimmun Rev. 2005 Jul;4(6):351-63. doi: 10.1016/j.autrev.2005.01.007. Epub 2005 Mar 7.
The crucial role of regulatory cells in self-tolerance and autoimmunity has been clearly established in numerous types of regulatory cells, the majority of which are CD4(+) T cells. Much focus has been placed on thymically derived CD4(+)CD25(+) regulatory T cells, given that the depletion of this subset in murine models results in the spontaneous development of autoimmune diseases. These naturally occurring regulatory T cells are found to be functionally mature in the thymus, and exert suppression in a contact-dependent manner. Another important category of immunosuppressive cells consists of conditionally induced regulatory T cells such as Tr1, Th3, and various other CD4(+) lymphocytes. Understanding the development and regulatory functions of immunoregulatory cells may elucidate the etiology for loss of self-tolerance. This review will summarize the characteristics, developmental pathways, and functions of regulatory T cells, as well as their role in human autoimmune diseases including multiple sclerosis, rheumatoid arthritis, Myasthenia Gravis, Kawasaki disease, autoimmune polyglandular syndrome type II, type 1 diabetes, autoimmune lymphoproliferative syndrome, and systemic lupus erythematosus.
调节性细胞在自身耐受和自身免疫中的关键作用已在多种类型的调节性细胞中得到明确证实,其中大多数是CD4(+) T细胞。鉴于在小鼠模型中去除这一亚群会导致自身免疫性疾病的自发发展,胸腺来源的CD4(+)CD25(+)调节性T细胞受到了很多关注。这些天然存在的调节性T细胞在胸腺中功能成熟,并以接触依赖的方式发挥抑制作用。另一类重要的免疫抑制细胞包括条件诱导的调节性T细胞,如Tr1、Th3和各种其他CD4(+)淋巴细胞。了解免疫调节细胞的发育和调节功能可能有助于阐明自身耐受丧失的病因。本综述将总结调节性T细胞的特征、发育途径和功能,以及它们在人类自身免疫性疾病中的作用,这些疾病包括多发性硬化症、类风湿性关节炎、重症肌无力、川崎病、II型自身免疫性多腺体综合征、1型糖尿病、自身免疫性淋巴增生综合征和系统性红斑狼疮。