Effects of IL-7 and dexamethasone:: Induction of CD25, the high affinity IL-2 receptor, on human CD4+ cells

被引:13
作者
Chung, IY
Dong, HF
Zhang, X
Hassanein, NMA
Howard, OMZ [1 ]
Oppenheim, JJ
Chen, X
机构
[1] Ctr Canc Res, Mol Immunoregulat Lab, Ft Detrick, MD 21702 USA
[2] SAIC Frederick Inc, Basic Res Program, Ft Detrick, MD 21702 USA
[3] Natl Canc Inst, Expt Immunol Lab, Ft Detrick, MD 21702 USA
关键词
CD4(+) CD25(+) regulatory T lymphocytes; dexamethasone; interleukin-7; suppression/anergy;
D O I
10.1016/j.cellimm.2005.01.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Since we have previously shown that dexamethasone (Dex) enhances the proportion of murine Treg cells, we tested the effect of IL-7, a promoter of T cell survival, together with Dex oil human CD4(+)CD25(+) Treg cells in an in vitro setting. The results showed that IL-7 in concert with Dex markedly augmented the generation of CD4(+)CD25(+) T cells. To discern the origin of the induced CD4(+)CD25(+) T cells, MACS-purified CD4(+)CD25(-), and CD4(+)CD25(+) cells were cultured in the presence of Dex and/or IL-7 for 4 days. Although two thirds of CD4(+)CD25(-) T cells became CD4(+)CD25(+) T cells, they had no Suppressive activity. In contrast, the original CD4(+)CD25(+) T cells maintained Suppressive activity after Dex/IL-7 treatment, however, there was not a significant expansion ill their cell number. Dex and IL-7 did not induce additional Treg cells, but additively induced the expression of the activation marker CD25 by CD4(+)CD25(-) T cells. This combination may provide a novel means of priming CD4 T cells to respond to IL-2 and may prove useful in up-regulation of normal immune responses in immune deficient diseases. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:57 / 63
页数:7
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