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Identification of CpG oligonucleotide sequences with high induction of IFN-alpha/beta in plasmacytoid dendritic cells
Author(s): Krug A, Rothenfusser S, Hornung V, Jahrsdorfer B, Blackwell S, Ballas ZK, Endres S, Krieg AM, Hartmann G
Source: EUROPEAN JOURNAL OF IMMUNOLOGY    Volume: 31    Issue: 7    Pages: 2154-2163    Published: JUL 2001  
Times Cited: 384     References: 53     
Abstract: The immature plasmacytoid dendritic cell (PDC) is identical with the principal type I IFN-producing cell upon viral infection. Oligodeoxynucleotides which contain unmethylated CpG motifs (CpG ODN) are recognized by the vertebrate immune system. Previously, we described CpG ODN that strongly activate human B cells and human blood dendritic cells. Mere we describe distinct CpG-containing oligonucleotide sequences which, in contrast to previously described CpG ODN, induced high amounts of IFN-cr and IFN-P in peripheral blood mononuclear cells (PBMC). Intracellular staining for IFN-a revealed that within PBMC CpG ODN-induced IFN-alpha is produced exclusively by PDC. Unlike IFN-cr, TNF-cr is upregulated in PDC by all CpG ODN tested. Purified PDC responded to CpG ODN, demonstrating direct activation of PDC by CpG ODN. The most active sequence induced the production of up to 5 pg: IFN-alpha per single PDC, resulting in more than 400 ng/ml IFN-alpha in the supernatant of PBMC enriched; for PDC. The potency of CpG ODN to stimulate IFN-a correlated with their ability to stimulate NK cell lytic activity, while purified NK cells did not respond. to CpG ODN. IFN-gamma production in PBMC was dependent on CpG ODN-induced IFN-alpha/beta as demonstrated by IFN-alpha/beta blocking antibodies. IFN-alpha -inducing CpG ODN strongly supported IFN-gamma production of TCR-triggered CD4 T cells but were less active than other CpG ODN in stimulating B cells. In conclusion our results demonstrate that particular CpG. ODN sequences exist which, due to high IFN-alpha/beta induction in PDC, induce a set of immune responses typical for viral infection.
Document Type: Article
Language: English
Reprint Address: Hartmann, G (reprint author), Klin Pharmakol Abt, Med Klin Innenstadt, Ziemssenstr 1, D-80336 Munich, Germany
Addresses:
1. Univ Munich, Dept Internal Med, Div Clin Pharmacol, Munich, Germany
2. Univ Iowa, Vet Affairs Med Ctr, Iowa City, IA USA
3. Univ Iowa, Dept Internal Med, Iowa City, IA USA
Publisher: WILEY-V C H VERLAG GMBH, PO BOX 10 11 61, D-69451 BERLIN, GERMANY
Subject Category: Immunology
IDS Number: 452DJ
ISSN: 0014-2980
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