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Synthetic Oligodeoxynucleotide CpG Motifs Activate Human Complement through Their Backbone Structure and Induce Complement-Dependent Cytokine Release

de Boer, Eline (författare)
Univ Oslo, Norway;Oslo Univ Hosp, Norway
Sokolova, Marina (författare)
Univ Oslo, Norway;Oslo Univ Hosp, Norway
Quach, Huy Q. (författare)
Univ Oslo, Norway;Oslo Univ Hosp, Norway,Linnaeus Ctr Biomat Chem, BMC
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McAdam, Karin E. (författare)
Univ Oslo, Norway;Oslo Univ Hosp, Norway
Gotz, Maximilian P. (författare)
Univ Copenhagen, Denmark
Chaban, Viktoriia (författare)
Univ Oslo, Norway;Oslo Univ Hosp, Norway
Vaage, Jarle (författare)
Univ Oslo, Norway;Oslo Univ Hosp, Norway
Fagerang, Beatrice (författare)
Univ Oslo, Norway;Oslo Univ Hosp, Norway
Woodruff, Trent M. (författare)
Univ Queensland, Australia
Garred, Peter (författare)
Univ Copenhagen, Denmark
Nilsson, Per H., 1980- (författare)
Linnéuniversitetet,Institutionen för kemi och biomedicin (KOB),Oslo Univ Hosp, Norway;Univ Oslo, Norway,Linnaeus Ctr Biomat Chem, BMC;HoRB
Mollnes, Tom E. (författare)
Univ Oslo, Norway;Oslo Univ Hosp, Norway;Nordland Hosp Bodo, Norway;Univ Tromso, Norway;Norwegian Univ Sci & Technol, Norway
Pischke, Soren E. (författare)
Univ Oslo, Norway;Oslo Univ Hosp, Norway
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 (creator_code:org_t)
2022-11-01
2022
Engelska.
Ingår i: Journal of Immunology. - : American Association of Immunologists. - 0022-1767 .- 1550-6606. ; 209:9, s. 1760-1767
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Bacterial and mitochondrial DNA, sharing an evolutionary origin, act as danger-associated molecular patterns in infectious and sterile inflammation. They both contain immunomodulatory CpG motifs. Interactions between CpG motifs and the complement system are sparsely described, and mechanisms of complement activation by CpG remain unclear. Lepirudin-anticoagulated human whole blood and plasma were incubated with increasing concentrations of three classes of synthetic CpGs: CpG-A, -B, and -C oligodeoxynucleotides and their GpC sequence controls. Complement activation products were analyzed by immunoassays. Cytokine levels were determined via 27-plex beads-based immunoassay, and CpG interactions with individual complement proteins were evaluated using magnetic beads coated with CpG-B. In whole blood and plasma, CpG-B and CpG-C (p < 0.05 for both), but not CpG-A (p > 0.8 for all), led to time- and dose-dependent increase of soluble C5b-9, the alternative complement convertase C3bBbP, and the C3 cleavage product C3bc. GpC-A, -B, and -C changed soluble fluid-phase C5b-9, C3bBbP, and C3bc to the same extent as CpG-A, -B, and -C, indicating a DNA backbone-dependent effect. Dose-dependent CpG-B binding was found to C1q (r = 0.83; p 5 0.006) and factor H (r = 0.93; p < 0.001). The stimulatory complement effect was partly preserved in C2-deficient plasma and completely preserved in MASP-2-deficient serum. CpG-B increased levels of IL-1 beta, IL-2, IL-6, IL-8, MCP-1, and TNF in whole blood, which were completely abolished by inhibition of C5 and C5aR1 (p < 0.05 for all). In conclusion, synthetic analogs of bacterial and mitochondrial DNA activate the complement system via the DNA backbone. We suggest that CpG-B interacts directly with classical and alternative pathway components, resulting in complement-C5aR1-dependent cytokine release.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Immunology in the medical area (hsv//eng)

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Immunologi
Immunology

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