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Cytokine profile in a cohort of healthy blood donors carrying polymorphisms in genes encoding the NLRP3 inflammasome

Sahdo, Berolla, 1984- (author)
Örebro universitet,Institutionen för hälsovetenskap och medicin,Örebro University, Sweden
Fransén, Karin, 1973- (author)
Örebro universitet,Institutionen för hälsovetenskap och medicin,Örebro University, Sweden
Asfaw Idosa, Berhane, 1977- (author)
Örebro universitet,Institutionen för hälsovetenskap och medicin,Örebro University, Sweden
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Eriksson, Per (author)
Östergötlands Läns Landsting,Linköpings universitet,Reumatologi,Hälsouniversitetet,Reumatologiska kliniken i Östergötland
Söderquist, Bo, 1955- (author)
Örebro universitet,Institutionen för läkarutbildning,Örebro University Hospital, Region Örebro County, Örebro, Sweden
Kelly, Anne, 1978- (author)
Örebro universitet,Institutionen för hälsovetenskap och medicin,Örebro University Hospital and Örebro University, Sweden
Särndahl, Eva, 1963- (author)
Örebro universitet,Institutionen för läkarutbildning,Örebro University, Sweden
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 (creator_code:org_t)
2013-10-03
2013
English.
In: PLOS ONE. - : Public Library of Science (PLoS). - 1932-6203. ; 8:10
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: The NLRP3 inflammasome has been recognized as one of the key components of the innate immunity by sensing a diversity of insults. Inflammasome activation results in the maturation of the pro-inflammatory cytokines interleukin (IL)-1 beta and IL-18. Increased production of IL-1 beta is found in patients with gain-of-function polymorphisms in genes encoding the NLRP3 inflammasome. Since approximately 5% of the Swedish population are heterozygote carriers of these combined gene variants, their impact on inflammasome status and a relationship on disease development is therefore highly relevant to study. The present study investigates levels of inflammasome-produced cytokines as a measure of inflammasome activation in healthy individuals carrying Q705K polymorphism in the NLRP3 gene combined with C10X in the CARD8 gene.Materials and Methods: Genotyping of 1006 healthy blood donors was performed for the polymorphisms Q705K in the NLRP3 and C10X in the CARD8 genes. IL-1 beta, IL-18, IL-33, as well as a number of other pro-inflammatory cytokines, were analyzed by Luminex or ELISA in plasma from individuals carrying the polymorphisms and in age and gender matched non-carrier controls.Results & Discussion: The prevalence of the polymorphisms was in line with previous studies. Plasma levels of IL-1 beta and IL-33 were elevated among carriers of combined Q705K+C10X polymorphisms compared to controls, whereas no difference was found for IL-18 and the other cytokines measured. Moreover, carriers of C10X or Q705K per se had similar plasma levels of IL-1 beta as non-carriers. These data suggest that the combined polymorphisms create inflammasomes with increased basal activation state, which might provide a more favourable innate immune response. In spite of this, it could also represent the mechanisms by which the inflammatory loop is triggered into a long-term inflammatory phenotype.

Subject headings

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)

Keyword

Medicine
Medicin

Publication and Content Type

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art (subject category)

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