Mechanisms for T cell tolerance induced with granulocyte colony-stimulating factor

被引:27
作者
Yang, Jian-Zhu [1 ]
Zhang, Jin-Qiao [2 ]
Sun, Li-Xia [2 ]
机构
[1] Hebei Med Univ, Dept Pathol, Affiliated Hosp 3, Shijiazhuang 050051, Peoples R China
[2] Hebei Med Univ, Dept Hematol, Affiliated Hosp 3, Shijiazhuang 050051, Peoples R China
关键词
Granulocyte colony-stimulating factor; Immune tolerance; T cells; Graft-versus-host disease; Autoimmune diseases; VERSUS-HOST-DISEASE; REGULATORY B-CELLS; BONE-MARROW GRAFTS; G-CSF; DENDRITIC CELLS; IMMUNE TOLERANCE; LOW-RISK; MYELOID CELLS; TRANSPLANTATION; MOBILIZATION;
D O I
10.1016/j.molimm.2015.12.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Granulocyte colony-stimulating factor (G-CSF) has been widely accepted as a mediator of T cell tolerance. The immune modulatory effect of G-CSF on T cells is believed to be mediated exclusively through other effector cells, such as monocytes, tolerogenic dendritic cells (DC), and myeloid-derived suppressor cells. Recent advances confirmed the direct effects of G-CSF in inducing immune tolerance of T cells through the G-CSF-G-CSF receptor pathway and related molecular mechanisms. This review aims to summarize the findings associated with the direct and indirect mechanisms for T cell tolerance induced with G-CSF. The role of G-CSF in preventing graft-versus-host disease (GVHD) and in treating autoimmune diseases (ADs) is also discussed. It is conceivable that G-CSF and immune cell compositions, such as tolerogenic DC and CD4(+)CD25(+)Foxp3(+) T cells, modulated by G-CSF could become an integral part of the immunomodulatory therapies against GVHD and ADs in the future. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:56 / 62
页数:7
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