Lutz Manfred B, Kurts Christian
Institute for Virology and Immunobiology, University of Würzburg, Würzburg, Germany.
Eur J Immunol. 2009 Sep;39(9):2325-30. doi: 10.1002/eji.200939548.
DC can present and cross-present self-antigens to autoreactive CD4(+) and CD8(+) T cells, respectively, and incapacitate them by inducing anergy, deletion or converting them into Treg. In this review, we summarize the recent progress in immune tolerance research, which has been achieved by employing antigen- and TCR-transgenic mice. We cover the numerous discoveries that have furthered our knowledge of the DC subsets and maturation pathways involved in tolerance; the signals, such as CD70, TGF-beta, B7-H1/PD-L1, which dictate the decision between immunity and tolerance; and the in vivo role of DC in the maintenance of CD4(+) T-cell tolerance and CD8(+) T-cell cross-tolerance.
树突状细胞(DC)可分别将自身抗原呈递给自身反应性CD4(+)和CD8(+) T细胞,并通过诱导无反应性、细胞凋亡或使其转化为调节性T细胞(Treg)来使其失能。在本综述中,我们总结了通过使用抗原和TCR转基因小鼠在免疫耐受研究方面取得的最新进展。我们涵盖了众多发现,这些发现加深了我们对参与耐受的DC亚群和成熟途径的了解;决定免疫和耐受之间抉择的信号,如CD70、转化生长因子-β(TGF-β)、B7-H1/程序性死亡受体-配体1(PD-L1);以及DC在维持CD4(+) T细胞耐受和CD8(+) T细胞交叉耐受中的体内作用。