| Literature DB >> 15699162 |
Takahiro Sugiyama1, Mayda Gursel, Fumihiko Takeshita, Cevayir Coban, Jacqueline Conover, Tsuneyasu Kaisho, Shizuo Akira, Dennis M Klinman, Ken J Ishii.
Abstract
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 unmethylated 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.Entities:
Mesh:
Substances:
Year: 2005 PMID: 15699162 DOI: 10.4049/jimmunol.174.4.2273
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422