Plasmacytoid dendritic cell-specific receptor ILT7-FcεRIγ inhibits Toll-like receptor-induced interferon production

被引:208
作者
Cao, Wei [1 ]
Rosen, David B.
Ito, Tomoki
Bover, Laura
Bao, Musheng
Watanabe, Gokuran
Yao, Zhengbin
Zhang, Li
Lanier, Lewis L.
Liu, Yong-Jun
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Immunol, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[3] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Biomed Sci Grad Program, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Canc Res Inst, San Francisco, CA 94143 USA
[6] Tanox Inc, Houston, TX 77025 USA
关键词
D O I
10.1084/jem.20052454
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Immunoglobulin-like transcripts are a family of inhibitory and stimulatory cell surface immune receptors. Transcripts for one member of this family, ILT7, are selectively expressed in human plasmacytoid dendritic cells ( pDCs). We demonstrate here that ILT7 protein associates with the signal adapter protein Fc epsilon RI gamma to form a receptor complex. Using an anti-ILT7 monoclonal antibody, we show that ILT7 is expressed specifically on human pDCs, but not on myeloid dendritic cells or other peripheral blood leukocytes. Cross-linking of ILT7 resulted in phosphorylation of Src family kinases and Syk kinase and induced a calcium influx in freshly isolated pDCs, which was blocked by Src family and Syk kinases inhibitors, thus indicating the activation of an immunoreceptor-based tyrosine activation motif mediated signaling pathway. ILT7 cross-linking on CpG or influenza virus-stimulated primary pDCs inhibited the transcription and secretion of type I interferon and other cytokines. Therefore, the ILT7-Fc epsilon RI gamma receptor complex negatively regulates the innate immune functions of human pDCs.
引用
收藏
页码:1399 / 1405
页数:7
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