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

被引:802
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
相关论文
共 32 条
[1]   REQUIREMENT FOR HLA-DR+ ACCESSORY CELLS IN NATURAL KILLING OF CYTOMEGALOVIRUS-INFECTED FIBROBLASTS [J].
BANDYOPADHYAY, S ;
PERUSSIA, B ;
TRINCHIERI, G ;
MILLER, DS ;
STARR, SE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1986, 164 (01) :180-195
[2]   Plasmacytoid dendritic cells activated by influenza virus and CD40L drive a potent THI polarization [J].
Cella, M ;
Facchetti, F ;
Lanzavecchia, A ;
Colonna, M .
NATURE IMMUNOLOGY, 2000, 1 (04) :305-310
[3]   Plasmacytoid monocytes migrate to inflamed lymph nodes and produce large amounts of type I interferon [J].
Cella, M ;
Jarrossay, D ;
Facchetti, F ;
Alebardi, O ;
Nakajima, H ;
Lanzavecchia, A ;
Colonna, M .
NATURE MEDICINE, 1999, 5 (08) :919-923
[4]  
CHEHIMI J, 1989, IMMUNOLOGY, V68, P488
[5]  
DALOD M, 2001, UNPUB IFN ALPHA BETA
[6]  
Eloranta ML, 1999, SCAND J IMMUNOL, V49, P391
[7]   Production of interferon-alpha/beta by murine dendritic cell lines stimulated by virus and bacteria [J].
Eloranta, ML ;
Sandberg, K ;
RicciardiCastagnoli, P ;
Lindahl, M ;
Alm, GV .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1997, 46 (03) :235-241
[8]   T cell memory: Heterogeneity and mechanisms [J].
Farber, DL .
CLINICAL IMMUNOLOGY, 2000, 95 (03) :173-181
[9]   HUMAN NATURAL INTERFERON-ALPHA PRODUCING CELLS [J].
FITZGERALDBOCARSLY, P .
PHARMACOLOGY & THERAPEUTICS, 1993, 60 (01) :39-62
[10]  
FLEMING TJ, 1993, J IMMUNOL, V151, P2399