A polymorphism in the IL11 gene is associated with ulcerative colitis
Inflammatory bowel diseases (IBD) are multifactorial disorders characterised by the host's inability to limit the inflammatory response to luminal antigens. The association of polymorphisms in the CARD15 gene with Crohn's disease (CD) demonstrates the relevance of activated transcription f...
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Veröffentlicht in: | Genes and immunity 2002-12, Vol.3 (8), p.494-496 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Inflammatory bowel diseases (IBD) are multifactorial disorders characterised by the host's inability to limit the inflammatory response to luminal antigens. The association of polymorphisms in the CARD15 gene with Crohn's disease (CD) demonstrates the relevance of activated transcription factor NF
κ
B in mononuclear cells. Interleukin 11 (IL11) mediates anti-inflammatory effects and is able to downregulate LPS-induced NF
κ
B activation. The
IL11
gene is therefore a good candidate involved in genetic predisposition to IBD. To evaluate the role of the
IL11
gene in IBD, two polymorphisms, including a dinucleotide repeat in the promoter region, have been genotyped in 222 patients with CD, 152 patients with ulcerative colitis (UC) and 400 healthy controls. PCR-SSCP analysis of the coding region revealed a single polymorphism in exon 4 leading to an amino acid exchange (G335A; R112H), not significantly associated with either disease. Dinucleotide repeat frequencies of the
IL11.A1
allele and of
IL11.A1
homozygous individuals were significantly increased among the patients with UC (
P |
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ISSN: | 1466-4879 1476-5470 |
DOI: | 10.1038/sj.gene.6363897 |