IL-12 up-regulates CD40 ligand (CD154) expression on human T cells

被引:0
|
作者
Peng, XH
Remacle, JE
Kasran, A
Huylebroeck, D
Ceuppens, JL
机构
[1] Catholic Univ Louvain, Fac Med, Dept Pathophysiol, Expt Immunol Lab, B-3000 Louvain, Belgium
[2] Catholic Univ Louvain VIB, Lab Cell Growth Differentiat & Dev, B-3000 Louvain, Belgium
来源
JOURNAL OF IMMUNOLOGY | 1998年 / 160卷 / 03期
关键词
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IL-12 is a heterodimeric cytokine produced by APC that promotes the development of CD4(+) Thl cells and their IFN-gamma production after TCR/CD3 triggering. We here investigated the capacity,, of IL-ll to modify the expression on T cells of CD40 ligand (CD40L or CD154), a molecule transiently expressed on activated T cells and known to be of utmost importance for cognate interaction with B cells and for activation of dendritic cells and macrophages. Our data demonstrate that IL-12 up-regulates CD40L expression on anti-CD3-activated human peripheral blood T cells, For optimal induction of CD40L. IL-12 synergizes with IL-2 as well as with other costimulatory interactions, such as B7/CD28. The effect of IL-12 was observed at both the protein and the mRNA level, T cells costimulated by IL-12 provided more efficient help for IL-4-dependent B cell proliferation and for Ige; production than when activated in the absence of IL-12. This helper activity was blocked by an mAb against CD40L, indicating that the effect of IL-12 on B cells is mediated indirectly through CD40L. The data thus suggest that the effects of IL-12 on cellular and humoral immune responses are partly mediated through CD40L induction.
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页码:1166 / 1172
页数:7
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