Common studied polymorphisms do not affect plasma cytokine levels upon endotoxin exposure in humans

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Common studied polymorphisms do not affect plasma cytokine levels upon endotoxin exposure in humans. / Taudorf, Sarah; Krabbe, K.S.; Berg, Ronan Martin Griffin; Møller, Kirsten; Pedersen, Bente Klarlund; Bruunsgaard, H.

I: Clinical and Experimental Immunology, Bind 152, Nr. 1, 2008, s. 147-152.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Taudorf, S, Krabbe, KS, Berg, RMG, Møller, K, Pedersen, BK & Bruunsgaard, H 2008, 'Common studied polymorphisms do not affect plasma cytokine levels upon endotoxin exposure in humans', Clinical and Experimental Immunology, bind 152, nr. 1, s. 147-152. https://doi.org/10.1111/j.1365-2249.2008.03612.x

APA

Taudorf, S., Krabbe, K. S., Berg, R. M. G., Møller, K., Pedersen, B. K., & Bruunsgaard, H. (2008). Common studied polymorphisms do not affect plasma cytokine levels upon endotoxin exposure in humans. Clinical and Experimental Immunology, 152(1), 147-152. https://doi.org/10.1111/j.1365-2249.2008.03612.x

Vancouver

Taudorf S, Krabbe KS, Berg RMG, Møller K, Pedersen BK, Bruunsgaard H. Common studied polymorphisms do not affect plasma cytokine levels upon endotoxin exposure in humans. Clinical and Experimental Immunology. 2008;152(1):147-152. https://doi.org/10.1111/j.1365-2249.2008.03612.x

Author

Taudorf, Sarah ; Krabbe, K.S. ; Berg, Ronan Martin Griffin ; Møller, Kirsten ; Pedersen, Bente Klarlund ; Bruunsgaard, H. / Common studied polymorphisms do not affect plasma cytokine levels upon endotoxin exposure in humans. I: Clinical and Experimental Immunology. 2008 ; Bind 152, Nr. 1. s. 147-152.

Bibtex

@article{43c12770f2b411ddbf70000ea68e967b,
title = "Common studied polymorphisms do not affect plasma cytokine levels upon endotoxin exposure in humans",
abstract = "The aim of this study was to investigate to what extent single nucleotide polymorphisms (SNPs) in promoter regions of genes of Toll-like receptor (TLR)-4, tumour necrosis factor (TNF)-alpha, interleukin (IL)-18, interferon (IFN)-gamma, IL-6 and IL-10 affect the cytokine response during a controlled low-grade inflammatory response in vivo. Two hundred healthy young male volunteers were genotyped, and cytokine levels were measured in response to a low-dose intravenous bolus of Escherichia coli endotoxin. No association was detected between SNPs (TLR-4299, TLR-4399, TNF-308, IL-18-137, IL-18-607, IFN-gamma+874, IL-6-174, IL-10-592 and IL-10-1082) and endotoxin-induced changes in plasma levels of TNF-alpha, IL-6 and IL-10. IL-18 levels were unaffected by endotoxin. In conclusion, the investigated SNPs did not affect endotoxin-induced low-grade cytokine production of TNF-alpha, IL-6, IL-18 or IL-10 in healthy young men. Previous reports of a major heritability factor in the inflammatory response may be due to other target genes or effects in older age groups or women Udgivelsesdato: 2008/4",
author = "Sarah Taudorf and K.S. Krabbe and Berg, {Ronan Martin Griffin} and Kirsten M{\o}ller and Pedersen, {Bente Klarlund} and H. Bruunsgaard",
year = "2008",
doi = "10.1111/j.1365-2249.2008.03612.x",
language = "English",
volume = "152",
pages = "147--152",
journal = "Clinical and Experimental Immunology, Supplement",
issn = "0964-2536",
publisher = "Wiley-Blackwell",
number = "1",

}

RIS

TY - JOUR

T1 - Common studied polymorphisms do not affect plasma cytokine levels upon endotoxin exposure in humans

AU - Taudorf, Sarah

AU - Krabbe, K.S.

AU - Berg, Ronan Martin Griffin

AU - Møller, Kirsten

AU - Pedersen, Bente Klarlund

AU - Bruunsgaard, H.

PY - 2008

Y1 - 2008

N2 - The aim of this study was to investigate to what extent single nucleotide polymorphisms (SNPs) in promoter regions of genes of Toll-like receptor (TLR)-4, tumour necrosis factor (TNF)-alpha, interleukin (IL)-18, interferon (IFN)-gamma, IL-6 and IL-10 affect the cytokine response during a controlled low-grade inflammatory response in vivo. Two hundred healthy young male volunteers were genotyped, and cytokine levels were measured in response to a low-dose intravenous bolus of Escherichia coli endotoxin. No association was detected between SNPs (TLR-4299, TLR-4399, TNF-308, IL-18-137, IL-18-607, IFN-gamma+874, IL-6-174, IL-10-592 and IL-10-1082) and endotoxin-induced changes in plasma levels of TNF-alpha, IL-6 and IL-10. IL-18 levels were unaffected by endotoxin. In conclusion, the investigated SNPs did not affect endotoxin-induced low-grade cytokine production of TNF-alpha, IL-6, IL-18 or IL-10 in healthy young men. Previous reports of a major heritability factor in the inflammatory response may be due to other target genes or effects in older age groups or women Udgivelsesdato: 2008/4

AB - The aim of this study was to investigate to what extent single nucleotide polymorphisms (SNPs) in promoter regions of genes of Toll-like receptor (TLR)-4, tumour necrosis factor (TNF)-alpha, interleukin (IL)-18, interferon (IFN)-gamma, IL-6 and IL-10 affect the cytokine response during a controlled low-grade inflammatory response in vivo. Two hundred healthy young male volunteers were genotyped, and cytokine levels were measured in response to a low-dose intravenous bolus of Escherichia coli endotoxin. No association was detected between SNPs (TLR-4299, TLR-4399, TNF-308, IL-18-137, IL-18-607, IFN-gamma+874, IL-6-174, IL-10-592 and IL-10-1082) and endotoxin-induced changes in plasma levels of TNF-alpha, IL-6 and IL-10. IL-18 levels were unaffected by endotoxin. In conclusion, the investigated SNPs did not affect endotoxin-induced low-grade cytokine production of TNF-alpha, IL-6, IL-18 or IL-10 in healthy young men. Previous reports of a major heritability factor in the inflammatory response may be due to other target genes or effects in older age groups or women Udgivelsesdato: 2008/4

U2 - 10.1111/j.1365-2249.2008.03612.x

DO - 10.1111/j.1365-2249.2008.03612.x

M3 - Journal article

VL - 152

SP - 147

EP - 152

JO - Clinical and Experimental Immunology, Supplement

JF - Clinical and Experimental Immunology, Supplement

SN - 0964-2536

IS - 1

ER -

ID: 10144321