Document Detail

Vitamin D status is not associated with inflammatory cytokine levels during experimental human endotoxaemia.
MedLine Citation:
PMID:  23286950     Owner:  NLM     Status:  MEDLINE    
Vitamin D has been shown to modulate innate immune responses in vitro and ex vivo; however, human in-vivo data are lacking. At high latitudes, seasonal vitamin D deficiency is common due to alternating ultraviolet (UV)-B radiation exposure. In the present study, we investigated whether levels of 25 hydroxyvitamin D(3) [25(OH)D(3) ] and its active metabolite 1,25 dihydroxyvitamin D(3) [1,25(OH)(2) D(3) ] are subject to seasonal variation and whether plasma levels of these vitamin D metabolites correlate with the in-vivo cytokine response during experimental human endotoxaemia [administration of lipopolysaccharide (LPS) in healthy volunteers]. Plasma levels of 25(OH)D(3) and 1,25(OH)(2) D(3) were determined in samples obtained just prior to administration of an intravenous bolus of 2 ng/kg LPS (derived from Escherichia coli O:113) in 112 healthy male volunteers. In the same subjects, plasma levels of the inflammatory cytokines tumour necrosis factor (TNF)-α, interleukin (IL)-6 and IL-10 were analysed serially after endotoxin administration. Plasma levels of 1,25(OH)(2) D(3) , but not 25(OH)D(3) , were subject to significant seasonal variation, with lower levels in autumn and winter. 25(OH)D(3) and 1,25(OH)(2) D(3) levels did not correlate with plasma cytokine responses. Furthermore, 25(OH)D(3) deficient subjects (< 50 nmol/l) displayed an identical cytokine response compared with sufficient subjects. In conclusion, plasma levels of vitamin D are not correlated with the LPS-induced TNF, IL-6 and IL-10 cytokine response in humans in vivo. These findings question the direct role of vitamin D in modulation of the innate immune response.
M Kox; M J W van den Berg; J G van der Hoeven; J P M Wielders; A J van der Ven; P Pickkers
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Clinical and experimental immunology     Volume:  171     ISSN:  1365-2249     ISO Abbreviation:  Clin. Exp. Immunol.     Publication Date:  2013 Feb 
Date Detail:
Created Date:  2013-01-04     Completed Date:  2013-03-12     Revised Date:  2014-02-04    
Medline Journal Info:
Nlm Unique ID:  0057202     Medline TA:  Clin Exp Immunol     Country:  England    
Other Details:
Languages:  eng     Pagination:  231-6     Citation Subset:  IM    
Copyright Information:
© 2012 British Society for Immunology.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Calcifediol / immunology,  metabolism*
Calcitriol / immunology,  metabolism*
Cytokines / blood,  immunology*
Endotoxemia / immunology*
Escherichia coli / immunology*
Immunity, Innate
Inflammation Mediators / metabolism
Lipopolysaccharides / immunology
Vitamin D / blood,  immunology*
Young Adult
Reg. No./Substance:
0/Cytokines; 0/Inflammation Mediators; 0/Lipopolysaccharides; 1406-16-2/Vitamin D; FXC9231JVH/Calcitriol; P6YZ13C99Q/Calcifediol

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Local and systemic effects of co-stimulatory blockade using cytotoxic T lymphocyte antigen-4-immunog...
Next Document:  Neutron diffraction study of triple-layered Sr(4)Ru(3)O(10).