Linking innate and acquired immunity: divergent role of CD46 cytoplasmic domains in T cell-induced inflammation

被引:148
作者
Marie, JC
Astier, AL
Rivailler, P
Rabourdin-Combe, C
Wild, TF
Horvat, B
机构
[1] CERVI, INSERM, U404, F-69365 Lyon 07, France
[2] CERVI, INSERM, U503, F-69365 Lyon 07, France
关键词
D O I
10.1038/ni810
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD46 is a widely expressed transmembrane protein that was initially identified as binding and inactivating C3b and C4b complement products. We used mice that were transgenic for one of two human CD46 isoforms that differ in their cytoplasmic domains (termed CD46-1 and CD46-2) to analyze the effect of CD46 stimulation on the immune response. We show here that CD46 can regulate inflammatory responses, either by inhibiting (CD46-1) or increasing (CD46-2) the contact hypersensitivity reaction. We found that engagement of CD46-1 or CD46-2 differentially affected CD8(+) T cell cytotoxicity, CD4(+) T cell proliferation, interleukin 2 (IL-2) and IL-10 production as well as tyrosine phosphorylation of Vav in T lymphocytes. These results indicate that CD46 plays a role in regulating the T cell-induced inflammatory reaction and in fine-tuning the cellular immune response by bridging innate and acquired immunity.
引用
收藏
页码:659 / 666
页数:8
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