Gilliet Michel, Liu Yong-Jun
DNAX Research Institute, Palo Alto, California, USA.
Hum Immunol. 2002 Dec;63(12):1149-55. doi: 10.1016/s0198-8859(02)00753-x.
Suppression by T-regulatory (Tr) cells is essential for the induction of T-cell tolerance and the prevention of autoimmune diseases, organ rejection, and graft-versus-host disease. Increasing attention has been devoted to understand the role of dendritic cells (DC) in the control of Tr-cell differentiation. Here we review the recent evidence that cluster designation (CD)40-ligand activated plasmacytoid-derived DCs (DC2) have the ability to induce primary Tr-cell differentiation. We propose that in addition to the regulatory functions of immature myeloid DC, Tr-cell induction by DC2 represents a nonredundant mechanism for the safeguard of peripheral T-cell tolerance. DC2 can be used as tool to drive potent antigen specific Tr-cell differentiation and expansion in vitro and in vivo.
调节性T(Tr)细胞的抑制作用对于诱导T细胞耐受性以及预防自身免疫性疾病、器官排斥反应和移植物抗宿主病至关重要。人们越来越关注了解树突状细胞(DC)在Tr细胞分化控制中的作用。在此,我们综述了近期的证据,即集群指定(CD)40配体激活的浆细胞样来源的DC(DC2)具有诱导原发性Tr细胞分化的能力。我们提出,除了未成熟髓样DC的调节功能外,DC2诱导Tr细胞代表了一种保障外周T细胞耐受性的非冗余机制。DC2可作为一种工具,在体外和体内驱动有效的抗原特异性Tr细胞分化和扩增。