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Peripheral Generation and Function of CD4+CD25+ Regulatory T Cells

机译:CD4 + CD25 +调节性T细胞的外周产生和功能

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The balance between immunity and tolerance is important to maintain immune homeostasis. Several mechanisms are in place to ensure that the immune response is controlled, such as T cell anergy, apoptosis and immune ignorance. A fourth mechanism of peripheral tolerance is the active suppression by regulatory or suppressor T cells. The existence of suppressor T cells was first described in the early 1970s, but these cells became discredited in the 1980s. The work of Shimon Sakaguchi and others, however, has brought these cells back into the limelight and nowadays research into regulatory/suppressor T cells is a very active field of immunology. Different types of regulatory T cells have been described, including CD4~+CD25~+ T cells that constitu-tively express CTLA-4, GITR and Foxp3, TGF-beta producing Th3 cells, IL-10 producing Trl cells, and CD8~+CD28~- T cells. This review will focus on the generation and function of CD4~+CD25~+ regulatory T cells. CD4~+CD25~+ regulatory cells were originally described as thymus-derived anergic/suppressive T cells. Recent papers, however, indicate that these cells might also be generated in the periphery, CD4~+CD25~+ regulatory T cells can be activated by self-antigens and non-self-antigens, and once activated can suppress T cells in an antigen nonspecific manner. Interestingly, the suppressive effects of these cells are not restricted to the adaptive immune system (T and B cells) but can also affect the activation and function of innate immune cells (monocytes, macrophages, dendritic cells). These features make the CD4~+CD25~+ regulatory T cell subset an interesting target for immunotherapy of chronic inflammatory or autoimmune diseases.
机译:免疫力和耐受力之间的平衡对于维持免疫稳态是重要的。有几种机制可以确保控制免疫反应,例如T细胞无反应性,细胞凋亡和免疫性无知。外周耐受的第四个机制是调节性或抑制性T细胞的主动抑制。抑制性T细胞的存在最早是在1970年代初被描述的,但是这些细胞在1980年代就被抹黑了。然而,Shimon Sakaguchi等人的工作使这些细胞重新成为人们关注的焦点,如今对调节性/抑制性T细胞的研究是免疫学中非常活跃的领域。已经描述了不同类型的调节性T细胞,包括组成性表达CTLA-4,GITR和Foxp3的CD4〜+ CD25〜+ T细胞,产生TGF-β的Th3细胞,产生IL-10的Trl细胞和CD8〜+ CD28〜-T细胞这项审查将侧重于CD4〜+ CD25〜+调节性T细胞的产生和功能。 CD4〜+ CD25〜+调节细胞最初被描述为源自胸腺的无反应/抑制性T细胞。然而,最近的论文表明,这些细胞也可能在外周产生,CD4〜+ CD25〜+调节性T细胞可以被自身抗原和非自身抗原激活,一旦被激活可以抑制抗原中的T细胞。非特定方式。有趣的是,这些细胞的抑制作用不仅限于适应性免疫系统(T细胞和B细胞),还可以影响先天免疫细胞(单核细胞,巨噬细胞,树突状细胞)的激活和功能。这些特征使CD4〜+ CD25〜+调节性T细胞亚群成为慢性炎性或自身免疫性疾病免疫治疗的有趣靶标。

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