CD47 ligation selectively inhibits the development of human naive T cells into Th1 effectors

被引:72
作者
Avice, MN
Rubio, M
Sergerie, M
Delespesse, G
Sarfati, M
机构
[1] Univ Montreal, Notre Dame Hosp, CHUM, Res Ctr,Allergy Res Lab, Montreal, PQ H3C 3J7, Canada
[2] Univ Montreal, Dept Obstet & Gynecol, Montreal, PQ H3C 3J7, Canada
关键词
D O I
10.4049/jimmunol.165.8.4624
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The CD47 Ag, also named integrin-associated protein, was recently reported to regulate the production of IL-12 by human monocytes and dendritic cells. The present study shows that CD47 ligation by CD47 mAb in primary cultures of cord blood mononuclear cells inhibits IL-12-driven Th1 cell development, as revealed by the cytokine secretion profile at restimulation and IFN-gamma production at the single-cell level. F(ab')(2) fragments of CD47 mAb or the synthetic peptide 4N1K, corresponding to the CD47 binding site of thrombospondin, display the same activity. CD47 engagement does not change the phenotype of IL-12-primed cells from Th1 to Th2 or affect IL-4-induced Th2 cell development. Moreover, CD47 mAb inhibits IL-12- but not IL-4-induced IL-2 production as well, as IFN-gamma in primary cultures, which was correlated with a decrease of the IL-12R beta 2 chain expression. Inclusion of exogenous IL-2 at priming corrects IL-12R expression as well as the inhibition of Th1 cell development. The data thus underline the role of IL-2 in Th1 cell development and further suggest that targeting IL-2 and IL-12 simultaneously may have some therapeutic advantage in Th1 autoimmune diseases.
引用
收藏
页码:4624 / 4631
页数:8
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