Analysis of the Foxp3/scurfin gene in Crohn's disease

Ogyi Park, Irina Grishina, Patrick S. Leung, M. Eric Gershwin, Thomas Prindiville

Research output: Contribution to journalArticle

Abstract

Crohn's disease (CD) is a chronic inflammatory bowel disease typified by transmural inflammation affecting any part of the gastrointestinal tract. CD4+CD25+ regulatory T cells (Treg cells) play important roles in intestinal homeostasis. Adoptive transfer of regulatory T cells into mice with chronic colitis prevented inflammation and reappearance of normal intestinal architecture. The Foxp3 gene encodes a protein that is a member of the forkhead/winged-helix family of transcriptional regulators and is involved in the regulation of T cell activation. Mutation of Foxp3 gene may lead to development of autoimmune disease and inflammatory bowel disease. We investigated 10 single-nucleotide polymorphisms (SNPs) of the Foxp3 gene in CD patients and assessed allele and genotype frequencies in 93 patients with Crohn's disease (61 female and 32 male), 82 patients with primary biliary cirrhosis (PBC) (all female), and 108 normal controls (51 female and 57 male). We found that 3 SNPs (-6054, -/ATT; -3279, A/C; -924, A/G) in the promoter region and 1 SNP (IVS9+459, T/C) in the intron 9 region existed in CD patients. No significant differences of allele and genotype frequencies of all four SNPs were observed between CD patients and controls (both female and male groups). However, there was a significance difference of the comparison between PBC patients and controls in the IVS9+459 SNP. These data indicate that SNPs of the Foxp3 gene are not significantly associated with CD but are associated with PBC.

Original languageEnglish (US)
Pages (from-to)218-228
Number of pages11
JournalAnnals of the New York Academy of Sciences
Volume1051
DOIs
StatePublished - 2005
Externally publishedYes

Fingerprint

Crohn Disease
Single Nucleotide Polymorphism
Genes
Polymorphism
Biliary Liver Cirrhosis
Regulatory T-Lymphocytes
Nucleotides
T-cells
Inflammatory Bowel Diseases
Gene Frequency
Genotype
Inflammation
Adoptive Transfer
Colitis
Genetic Promoter Regions
Introns
Autoimmune Diseases
Gastrointestinal Tract
Crohn's Disease
Gene

Keywords

  • Crohn's disease
  • Forkhead/winged helix box
  • Foxp3
  • Primary biliary cirrhosis
  • Regulatory T cells
  • Single-nucleotide polymorphism
  • T cells

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)

Cite this

Park, O., Grishina, I., Leung, P. S., Gershwin, M. E., & Prindiville, T. (2005). Analysis of the Foxp3/scurfin gene in Crohn's disease. Annals of the New York Academy of Sciences, 1051, 218-228. https://doi.org/10.1196/annals.1361.125

Analysis of the Foxp3/scurfin gene in Crohn's disease. / Park, Ogyi; Grishina, Irina; Leung, Patrick S.; Gershwin, M. Eric; Prindiville, Thomas.

In: Annals of the New York Academy of Sciences, Vol. 1051, 2005, p. 218-228.

Research output: Contribution to journalArticle

Park, O, Grishina, I, Leung, PS, Gershwin, ME & Prindiville, T 2005, 'Analysis of the Foxp3/scurfin gene in Crohn's disease', Annals of the New York Academy of Sciences, vol. 1051, pp. 218-228. https://doi.org/10.1196/annals.1361.125
Park, Ogyi ; Grishina, Irina ; Leung, Patrick S. ; Gershwin, M. Eric ; Prindiville, Thomas. / Analysis of the Foxp3/scurfin gene in Crohn's disease. In: Annals of the New York Academy of Sciences. 2005 ; Vol. 1051. pp. 218-228.
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