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A common CTLA4 haplotype associated with coeliac disease


Hunt, KA and McGovern, DPB and Kumar, PJ and Ghosh, S and Travis, SPL and Walters, JRF and Jewell, DP and Playford, RJ and van Heel, DA, A common CTLA4 haplotype associated with coeliac disease, European Journal of Human Genetics, 13, (4) pp. 440-444. ISSN 1018-4813 (2005) [Refereed Article]

DOI: doi:10.1038/sj.ejhg.5201357


Coeliac disease is a common enteropathy with a strong inherited risk characterised by dietary wheat, rye and barley induced T-cell activation. Although there is replicated linkage to 2q33, results are inconsistent from association studies of the most promising candidate genes: the CD28/CTLA4/ICOS cluster. CTLA4 plays a key role in regulating T lymphocyte mediated inflammatory responses, and variants in the 3′ region influence development of diabetes and thyroid disease. We genotyped CTLA4 variants (- 1722 C/T, -658 T/C, -318 C/T, +49 A/G, +1822 C/T, CT60 A/G) to tag all common haplotypes (> 5% frequency) and an ICOS variant (IVS + 173 C/T) in 340 white UK Caucasian coeliac disease cases. Strict ascertainment criteria for coeliac cases required both villous atrophy at diagnosis and positive serology. In total, 973 healthy controls were available for SNP, and 705 for CTLA4 haplotype, based association analyses. Coeliac disease showed weak association with the CTLA4 + 1822T (P=0.019) and CT60 G (P=0.047) alleles. Strong association was seen with a common CTLA4 haplotype (P=0.00067, odds ratio 1.41) of frequency 32.7% in coeliac disease and 25.5% in healthy controls. A common CTLA4 haplotype shows strong association with coeliac disease, and contains multiple alleles reported to affect immunological function. Loss of tolerance to dietary antigens in coeliac disease may be mediated in part by heritable variants in co-signalling genes regulating T-cell responses. © 2005 Nature Publishing Group All rights reserved.

Item Details

Item Type:Refereed Article
Research Division:Biomedical and Clinical Sciences
Research Group:Clinical sciences
Research Field:Gastroenterology and hepatology
Objective Division:Health
Objective Group:Clinical health
Objective Field:Clinical health not elsewhere classified
UTAS Author:Playford, RJ (Professor Ray Playford)
ID Code:72928
Year Published:2005
Web of Science® Times Cited:67
Deposited By:Research Division
Deposited On:2011-09-05
Last Modified:2011-09-05

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