Miyara Makoto, Sakaguchi Shimon
Department of Experimental Pathology, Institute for Frontier Medical Science, Kyoto University, Kyoto 606-8507, Japan.
Trends Mol Med. 2007 Mar;13(3):108-16. doi: 10.1016/j.molmed.2007.01.003. Epub 2007 Jan 24.
Natural FOXP3+CD25+CD4+ regulatory T cells (Tregs) actively suppress pathological and physiological immune responses, contributing to the maintenance of immunological self-tolerance and immune homeostasis. Various molecular and cellular events have been described to explain the mechanism(s) of Treg-mediated suppression. However, none of the proposed mechanisms can explain all aspects of suppression. It is probable that various combinations of several mechanisms are operating, depending on the milieu and the type of immune responses, although there might be a single key mechanism that has a predominant role. Further studies of suppression and search for Treg-specific cell surface molecules are required for potential clinical application to treat and prevent immunological diseases and to control immune responses for the benefit of the host.
天然的FOXP3 + CD25 + CD4 +调节性T细胞(Tregs)可积极抑制病理性和生理性免疫反应,有助于维持免疫自身耐受性和免疫稳态。已描述了各种分子和细胞事件来解释Treg介导的抑制机制。然而,所提出的机制均无法解释抑制的所有方面。虽然可能存在一种起主要作用的关键机制,但很可能是几种机制的各种组合在起作用,这取决于环境和免疫反应的类型。为了在治疗和预防免疫性疾病以及控制免疫反应以利于宿主方面的潜在临床应用,需要对抑制作用进行进一步研究并寻找Treg特异性细胞表面分子。