SAGE library screening reveals ILT7 as a specific plasmacytoid dendritic cell marker that regulates type IIFN production

被引:30
作者
Cho, Minkwon [1 ]
Ishida, Koji [1 ]
Chen, Jingtao [1 ]
Ohkawa, Jun [1 ]
Chen, Wei [2 ]
Namiki, Sahori [1 ]
Kotaki, Ayumi [1 ]
Arai, Naoko [1 ]
Arai, Ken-ichi [1 ,3 ]
Kamogawa-Schifter, Yumiko [1 ,3 ]
机构
[1] Ginkgo Biomed Res Inst, Dept Immunobiol, Tokyo, Japan
[2] Univ Minnesota, Ctr Canc, Div Hematol Oncol & Bone Marrow Transplantat, Dept Pediat, Minneapolis, MN USA
[3] Univ Tokyo, Adv Sci & Technol Res Ctr, Tokyo, Japan
关键词
IFN; ILT7; pDC; SAGE;
D O I
10.1093/intimm/dxm127
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Plasmacytoid dendritic cells (pDCs) link innate to acquired immune responses by producing high levels of type I IFN upon infection. In order to identify the specific genes that control pDC, we compared serial analysis of gene expression libraries from human pDCs, herpes simplex virus-stimulated pDCs and monocytes. We found that Ig-like transcript ILT7 is specifically expressed on pDC cell surfaces and is down-regulated when pDC mature in response to viral or bacterial stimulation. ILT7 expression on the cell surface required association with the Fc epsilon RI gamma adaptor molecule. Although treatment with one anti-ILT7-specific mAb suppressed type I IFN production in response to cytosine-phosphate-guanosice (CpG) stimulation, another anti-ILT7 mAb up-regulated type I IFN production. We conclude that ILT7 is a key regulator of human pDC function.
引用
收藏
页码:155 / 164
页数:10
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