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
相关论文
共 23 条
[1]   Regulation of cytokine and cytokine receptor expression by glucocorticoids [J].
Almawi, WY ;
Beyhum, HN ;
Rahme, AA ;
Rieder, MJ .
JOURNAL OF LEUKOCYTE BIOLOGY, 1996, 60 (05) :563-572
[2]  
ARMITAGE RJ, 1990, J IMMUNOL, V144, P938
[3]   CD4+CD25high regulatory cells in human peripheral blood [J].
Baecher-Allan, C ;
Brown, JA ;
Freeman, GJ ;
Hafler, DA .
JOURNAL OF IMMUNOLOGY, 2001, 167 (03) :1245-1253
[4]   Molecular mechanisms of anti-inflammatory action of glucocorticoids [J].
Cato, ACB ;
Wade, E .
BIOESSAYS, 1996, 18 (05) :371-378
[5]   INTERLEUKIN-7 IS A T-CELL GROWTH-FACTOR [J].
CHAZEN, GD ;
PEREIRA, GMB ;
LEGROS, G ;
GILLIS, S ;
SHEVACH, EM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (15) :5923-5927
[6]   Differential response of murine CD4+CD25+ and CD4+CD25- T cells to dexamethasone-induced cell death [J].
Chen, X ;
Murakami, T ;
Oppenheim, JJ ;
Howard, DMZ .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2004, 34 (03) :859-869
[7]   Positive effects of glucocorticoids on T cell function by up-regulation of IL-7 receptor α [J].
Franchimont, D ;
Galon, J ;
Vacchio, MS ;
Fan, S ;
Visconti, R ;
Frucht, DM ;
Geenen, V ;
Chrousos, GP ;
Ashwell, JD ;
O'Shea, JJ .
JOURNAL OF IMMUNOLOGY, 2002, 168 (05) :2212-2218
[8]  
Khaled AR, 2002, BIOTECHNIQUES, P40
[9]   Identification of a novel glucocorticoid response unit (GRU) in the 5′-flanking region of the mouse IL-2 receptor α gene [J].
Lamas, M ;
Campos, JR ;
Silva, AG .
CYTOKINE, 1997, 9 (12) :973-981
[10]   GLUCOCORTICOID HORMONES UP-REGULATE INTERLEUKIN-2 RECEPTOR-ALPHA GENE-EXPRESSION [J].
LAMAS, M ;
SANZ, E ;
MARTINPARRAS, L ;
ESPEL, E ;
SPERISEN, P ;
COLLINS, M ;
SILVA, AG .
CELLULAR IMMUNOLOGY, 1993, 151 (02) :437-450