Division of Rheumatology, Dept of Medicine at the David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095-1670, USA.
Autoimmun Rev. 2010 Jun;9(8):560-8. doi: 10.1016/j.autrev.2010.03.006. Epub 2010 Apr 10.
While CD4(+)CD25(high) regulatory T cells (Tregs) have garnered much attention for their role in the maintenance of immune homeostasis, recent findings have shown that subsets of CD8(+) T cells (CD8(+) Tregs) display immunoregulatory functions as well. Both CD4(+) Tregs and CD8(+) Tregs appear impaired in number and/or function in several autoimmune diseases and in experimental animal models of autoimmunity, suggesting the possibility of immunotherapeutic targeting of these cells for improved management of autoimmune conditions. Our group has developed a strategy to induce CD8(+) Tregs in autoimmune mice through the use of a tolerogenic self-peptide, and new information has been gained on the phenotype, function and role of induced CD8(+) Tregs in autoimmunity. Here we present an overview of the role and mechanisms of action of CD8(+) Tregs in autoimmunity, with a special focus on lupus. We also discuss the potential role of CD8(+) Tregs in other diseases, including chronic infection and cancer.
虽然 CD4(+)CD25(high) 调节性 T 细胞 (Tregs) 因其在维持免疫稳态中的作用而备受关注,但最近的研究结果表明,CD8(+)T 细胞 (CD8(+)Tregs) 的亚群也具有免疫调节功能。在几种自身免疫性疾病和自身免疫性实验动物模型中,CD4(+)Tregs 和 CD8(+)Tregs 的数量和/或功能似乎都受到了损害,这表明针对这些细胞进行免疫治疗的可能性,以改善自身免疫性疾病的治疗效果。我们的研究小组开发了一种通过使用耐受原性自身肽在自身免疫小鼠中诱导 CD8(+)Tregs 的策略,并获得了有关诱导的 CD8(+)Tregs 在自身免疫中的表型、功能和作用的新信息。本文概述了 CD8(+)Tregs 在自身免疫中的作用和作用机制,特别关注狼疮。我们还讨论了 CD8(+)Tregs 在其他疾病中的潜在作用,包括慢性感染和癌症。