Regulation of TGF-β response during T cell activation is modulated by IL-10

被引:141
|
作者
Cottrez, F [1 ]
Groux, H [1 ]
机构
[1] INSERM, U343, F-06200 Nice, France
来源
JOURNAL OF IMMUNOLOGY | 2001年 / 167卷 / 02期
关键词
D O I
10.4049/jimmunol.167.2.773
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
TGF-beta1 is an important pleiotropic cytokine that has been described to have both stimulatory and inhibitory effects on cell growth and differentiation. For several cell types, the effect of TGF-beta1 was found to correlate with the differentiation stage of the cells and the presence of other cytokines. In this report, we address the influence of TGF-beta1 on CD4(+) T cell activation by evaluating the effect of TGF-PI on the proliferative and cytokine responses of purified resting and activated human or mouse CD4(+) T cells. TGF-beta1 inhibits proliferation and cytokine secretion on resting CD4(+) T cells but has no inhibitory effect on activated T cells. Moreover, TGF-beta1 unresponsiveness of activated T cells was correlated with a down-regulation in the expression of the TGF-beta receptor type II. Interestingly, IL-10 addition enhances TGF-beta receptor type II expression and restores TGF-beta responsiveness on activated T cells. These results indicated that TGF-beta responsiveness is sequentially regulated on T cells by the modulation of the of TGF-beta receptor type II chain expression. Moreover, we have identified a novel regulatory role of IL-10 on TGF-beta -dependent T cell growth that can explain the control of T cell activation on chronic vs acute inflammatory sites.
引用
收藏
页码:773 / 778
页数:6
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