Mouse type IIFN-producing cells are immature APCs with plasmacytoid morphology

被引:798
作者
Asselin-Paturel, C
Boonstra, A
Dalod, M
Durand, I
Yessaad, N
Dezutter-Dambuyant, C
Vicari, A
O'Garra, A
Biron, C
Brière, F
Trinchieri, G [1 ]
机构
[1] Schering Plough Corp, Lab Immunol Res, Dardilly, France
[2] DNAX Res Inst Molec & Cellular Biol Inc, Dept Immunobiol, Palo Alto, CA USA
[3] Brown Univ, Dept Mol Microbiol & Immunol, Div Biol & Med, Providence, RI 02912 USA
[4] Ctr Hosp Edouard Herriot, INSERM Unite 346, Lyon, France
关键词
D O I
10.1038/ni736
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
dWe show here that mouse interferon-alpha (IFN-alpha)-producing cells (mIPCs) are a unique subset of immature antigen-presenting cells (APCs) that secrete IFN-alpha upon stimulation with viruses.. mIPCs have a plasmacytoid morphology, can be stained with an antibody to Ly6G and Ly6C (anti-Ly6G/C) and are Ly6C(+)B220(+)CDIIc(10)CD4(+); unlike other dendritic cell subsets, however, they do not express CD8 alpha or CDIIb. Although mIPCs undergo apoptosis in vitro, stimulation with viruses, IFN-alpha or CpG oligonucleotides enhanced their survival and T cell stimulatory activity. In vivo, mIPCs were the main producers of IFN-alpha in cytomegalovirus-infected mice, as depletion of Ly6G(+)/C+ cells abrogated IFN-alpha production. mIPCs produced interleukin 12 (IL-12) in response to viruses and CpG oligodeoxynucleotides, but not bacterial products. Although different pathogens can selectively engage various APC subsets for IL-12 production, IFN-alpha production is restricted to mIPCs' response to viral infection.
引用
收藏
页码:1144 / 1150
页数:7
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