The impact of interleukin-6 promoter -597/-572/-174 genotype on interleukin-6 production after lipopolysaccharide stimulation

被引:26
|
作者
Mueller-Steinhardt, M.
Ebel, B.
Haertel, C.
机构
[1] Heidelberg Univ, Inst Transfus Med & Immunol, Fac Med, D-68167 Mannheim, Germany
[2] Med Univ Lubeck, Inst Immunol & Transfus Med, Sch Med, D-23538 Lubeck, Germany
[3] Med Univ Lubeck, Dept Pediat, Sch Med, D-23538 Lubeck, Germany
来源
CLINICAL AND EXPERIMENTAL IMMUNOLOGY | 2007年 / 147卷 / 02期
关键词
-597/-572/-174genotype; interleukin-6; promoter polymorphism;
D O I
10.1111/j.1365-2249.2006.03273.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interleukin (IL)-6 is a pleiotropic cytokine, produced by different cells. There is accumulating evidence that IL-6 promoter polymorphisms impact substantially on various diseases and we identified kidney transplant recipients carrying the IL-6 GGG/GGG (-597/-572/-174)genotype to have superior graft survival. To prove a functional impact on gene expression, we analysed systematically IL-6 production in healthy individuals with respect to the IL-6 (-597/-572/-174)genotype. IL-6 was determined in 100 healthy blood donors at protein and mRNA levels upon specific stimulation in monocytes and T lymphocytes under whole blood conditions. GGG/GGG individuals showed a lower IL-6 secretion upon lipopolysaccharide (LPS)-stimulation versus all others (P = 0.039). This link was even stronger when (-597) and (-174)GG genotypes were reanalysed separately (P = 0.008, P = 0.017). However, we found neither a difference at the mRNA level or percentage of CD14(+) cells nor after T cell stimulation. We found evidence for the IL-6 (-597/-572/-174)genotype to affect IL-6 synthesis, i.e. lower levels of IL-6 protein upon LPS-stimulation in GGG/GGG individuals. Further studies are needed in kidney transplant recipients to investigate the potential link between the GGG/GGG genotype and graft survival. In line with this, determination of the genetic risk profiles might be promising to improve the transplant outcome in the individual patient.
引用
收藏
页码:339 / 345
页数:7
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