Characterization of a new human B7-related protein: B7RP-1 is the ligand to the co-stimulatory protein ICOS

被引:104
作者
Yoshinaga, SK [1 ]
Zhang, M
Pistillo, J
Horan, T
Khare, SD
Miner, K
Sonnenberg, M
Boone, T
Brankow, D
Dai, TN
Delaney, J
Han, H
Hui, A
Kohno, T
Manoukian, R
Whoriskey, JS
Coccia, MA
机构
[1] Amgen Inc, Exploratory Res, Thousand Oaks, CA 91320 USA
[2] Amgen Inc, Pharmacol, Thousand Oaks, CA 91320 USA
[3] Amgen Inc, Proc Dev, Thousand Oaks, CA 91320 USA
关键词
antigen-presenting cells; dendritic cells; cytokines; co-stimulation; TCR;
D O I
10.1093/intimm/12.10.1439
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Optimal T cell activation requires the interactions of co-stimulatory molecules, such as those in the CD28 and B7 protein families. Recently, we described the co-stimulatory properties of the murine ligand to ICOS, which we designated as B7RP-1, Here, we report the co-stimulation of human T cells through the human B7RP-1 and ICOS interaction. This ligand-receptor pair interacts with a K-D similar to 33 nM and an off-rate with a t(1/2) > 10 min. Interestingly, tumor necrosis factor (TNF)alpha differentially regulates the expression of human B7RP-1 on B cells, monocytes and dendritic cells (DC). TNF-alpha enhances B7RP-1 expression on B cells and monocytes, while it inhibits it on DC. The human B7RP-1-Fc protein or cells that express membrane-bound B7RP-1 co-stimulate T cell proliferation in vitro. Specific cytokines, such as IFN-gamma and IL-10, are induced by B7RP-1 co-stimulation, Although IL-2 levels are not significantly increased, B7RP-1 co-stimulation is dependent on IL-2, These experiments define the human ortholog to murine B7RP-1 and characterize its interaction with human ICOS.
引用
收藏
页码:1439 / 1447
页数:9
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