CpG RNA:: Identification of novel single-stranded RNA that stimulates human CD14+CD11c+ monocytes

被引:70
作者
Sugiyama, T
Gursel, M
Takeshita, F
Cohan, C
Conover, J
Kaisho, T
Akira, S
Klinman, DM
Ishii, KJ
机构
[1] Osaka Univ, Microbial Dis Res Inst, Dept Host Def, Suita, Osaka 5650871, Japan
[2] US FDA, Ctr Biol Evaluat & Res, Div Viral Prod, Sect Retroviral Immunol, Bethesda, MD 20892 USA
[3] RIKEN, Res Ctr Allergy & Immunol, Lab Host Def, Yokohama, Kanagawa, Japan
[4] Yokohama City Univ, Sch Med, Dept Mol Biodef Res, Yokohama, Kanagawa 232, Japan
[5] Osaka Univ, Japan Sci & Technol Agcy, Osaka, Japan
关键词
D O I
10.4049/jimmunol.174.4.2273
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Synthetic immunostimulatory nucleic acids such as CpG DNA are being harnessed therapeutically as vaccine adjuvants, anticancer or antiallergic agents. Efforts to identify nucleic acid-based agents capable of more specifically modulating the immune system are being developed. The current study identifies a novel class of single-stranded oligoribonucleotides (ORN) containing umnethylated CpG motifs and a poly(G) run at the 3' end (CpG ORN) that directly stimulate human CD14(+)CD11c(+) monocytes but not dendritic cells or B cells. CpG ORN activate NF-kappaB and p38 MAPK, resulting in IL-6 and IL-12 production and costimulatory molecule up-regulation but not IFNalpha. Methylation of cytosine at the 5' portion in core CpG motif abrogates such activation. TLR3, 7, 8, or 9 alone did not confer response to CpG ORN, in contrast to previously reported respective nucleic acid ligands. These data suggest that CpG ORN represent a novel class of synthetic immunostimulatory nucleic acids with distinct target cells, receptors, and functions from that of previously known immunomodulatory nucleic acids.
引用
收藏
页码:2273 / 2279
页数:7
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