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CpG-A and CpG-B oligonucleotides differentially enhance human peptide-specific primary and memory CD8+ T-cell responses in vitro.
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2004 (English)In: Blood, ISSN 0006-4971, E-ISSN 1528-0020, Vol. 103, no 6, 2162-9 p.Article in journal (Refereed) Published
Abstract [en]

Two distinct types of CpG oligodeoxynucleotide (ODN) have been identified that differ in their capacity to stimulate antigen-presenting cells: CpG-A induces high amounts of interferon-alpha (IFN-alpha) and IFN-beta in plasmacytoid dendritic cells (PDCs), whereas CpG-B induces PDC maturation and is a potent activator of B cells but stimulates only small amounts of IFN-alpha and IFN-beta. Here we examined the ability of these CpG ODNs to enhance peptide-specific CD8+ T-cell responses in human peripheral blood mononuclear cells (PBMCs). The frequency of influenza matrix-specific "memory" CD8+ T cells was increased by both types of CpG ODN, whereas the frequency of Melan-A specific "naive" CD8+ T cells increased on stimulation with CpG-B but not with CpG-A. The presence of PDCs in PBMCs was required for this CpG ODN-mediated effect. The expanded cells were cytotoxic and produced IFN- on peptide restimulation. Soluble factors induced by CpG-A but not CpG-B increased the granzyme-B content and cytotoxicity of established CD8+ T-cell clones, each of which was IFN-alpha/-beta dependent. In conclusion, CpG-B seems to be superior for priming CD8+ T-cell responses, and CpG-A selectively enhances memory CD8+ T-cell responses and induces cytotoxicity. These results demonstrate distinct functional properties of CpG-A and CpG-B with regard to CD8 T cells.

Place, publisher, year, edition, pages
2004. Vol. 103, no 6, 2162-9 p.
National Category
Clinical Medicine
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URN: urn:nbn:se:uu:diva-161368DOI: 10.1182/blood-2003-04-1091PubMedID: 14630815OAI: oai:DiVA.org:uu-161368DiVA: diva2:456008
Available from: 2011-11-11 Created: 2011-11-11 Last updated: 2017-12-08

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Lubenow, Norbert

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