Shevach Ethan M
Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Immunity. 2009 May;30(5):636-45. doi: 10.1016/j.immuni.2009.04.010.
Foxp3(+) T regulatory (Treg) cells control all aspects of the immune response. Here, I will review the in vitro model systems that have been developed to define the mechanisms used by Treg cells to suppress a large number of distinct target cell types. These mechanisms can be broadly divided into those that target T cells (suppressor cytokines, IL-2 consumption, cytolysis) and those that primarily target antigen-presenting cells (decreased costimulation or decreased antigen presentation). Although multiple mechanisms for Treg cell suppression have been shown in vitro, it is unclear whether the same or different mechanisms are used by Treg cells in vivo. An increase in our understanding of Treg cell suppressor mechanisms will offer an insight into how Treg cell function can be manipulated either positively or negatively in vivo.
叉头框蛋白3(Foxp3)阳性调节性T(Treg)细胞控制着免疫反应的各个方面。在此,我将综述已开发出的体外模型系统,这些系统用于确定Treg细胞抑制大量不同靶细胞类型所采用的机制。这些机制大致可分为针对T细胞的机制(抑制性细胞因子、白细胞介素-2消耗、细胞溶解)和主要针对抗原呈递细胞的机制(共刺激减少或抗原呈递减少)。尽管在体外已证明Treg细胞存在多种抑制机制,但尚不清楚Treg细胞在体内是否使用相同或不同的机制。对Treg细胞抑制机制的深入了解将有助于洞察如何在体内正向或负向操纵Treg细胞的功能。