High level IL-12 production by murine dendritic cells: Upregulation via MHC class II and CD40 molecules and downregulation by IL-4 and IL-10

被引:815
作者
Koch, F
Stanzl, U
Jennewein, P
Janke, K
Heufler, C
Kampgen, E
Romani, N
Schuler, G
机构
[1] UNIV ERLANGEN NURNBERG, DEPT DERMATOL, D-91052 ERLANGEN, GERMANY
[2] UNIV INNSBRUCK, DEPT DERMATOL, A-6020 INNSBRUCK, AUSTRIA
[3] UNIV WURZBURG, D-8700 WURZBURG, GERMANY
关键词
D O I
10.1084/jem.184.2.741
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have shown previously that dendritic cells (DC) produce IL-12 upon interaction with CD4+ T cells. Here we ask how this IL-12 production is induced and regulated. Quantitative PCR and in situ hybridization for IL-12 p40 and an ELISA specific for the F70 heterodimer were used to determine IL-12 production. We demonstrate that ligation of either CD40 or MHC class II molecules independently trigger IL-12 production ill DC, and that IL-12 production is downregulated by IL-4 and IL-10. The levels of bioactive IL-12. that can be released by triggering with all anti-CD40 mAb or with a T cell hybridoma are high (range 260-4700 pg/ml from 1 x 10(6) DC in 72 h). The CD40-mediated pathway indicates that IL-12. production is induced in DC upon interaction with activated, CD40 ligand-expressing helper T cells, even in the absence of cognate antigen recognition. Side-by-side comparison of IL-12 production, and blocking experiments employing an anti-CD40 ligand mAb, suggest that the CD40-mediated pathway is quantitatively more significant than induction via the MHC class II molecule. The importance of the CD40/CD40 ligand interaction for IL-12 induction in DC likely contributes to the recent finding that mice lacking the CD40 ligand are impaired in mounting Th1 type cell-mediated immune responses.
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页码:741 / 746
页数:6
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