Candidate gene region 2q33 in European families with coeliac disease

被引:34
作者
Holopainen, P
Naluai, ÅT
Moodie, S
Percopo, S
Coto, I
Clot, F
Ascher, H
Sollid, L
Ciclitira, P
Greco, L
Clerget-Darpoux, F
Partanen, J
机构
[1] Finnish Red Cross & Blood Transfus Serv, Dept Tissue Typing, SF-00310 Helsinki, Finland
[2] Finnish Red Cross & Blood Transfus Serv, Res Lab, SF-00310 Helsinki, Finland
[3] Goteborg Univ Sahlgrenska, Univ Hosp Ostra, Sahlgrenska Acad, Dept Clin Genet, Gothenburg, Sweden
[4] St Thomas Hosp, Rayne Inst, GKT, Gastroenterol Unit, London, England
[5] Univ Naples Federico II, Dept Paediat, I-80138 Naples, Italy
[6] Univ Naples Federico II, Int Lab Food Induced Dis, I-80138 Naples, Italy
[7] INSERM, U535, F-94275 Le Kremlin Bicetre, France
[8] Gothenburg Univ, Sahlgrenska Acad, Dept Paediat, Queen Silvia Childrens Hosp, Gothenburg, Sweden
[9] Univ Oslo, Rikshosp, Univ Hosp, Inst Immunol, N-0027 Oslo, Norway
来源
TISSUE ANTIGENS | 2004年 / 63卷 / 03期
关键词
autoimmunity; coeliac disease; CTLA-4; genetic susceptibility; T lymphocytes;
D O I
10.1111/j.1399-0039.2004.00189.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Chromosome region 2q33 harbours a cluster of genes, CTLA-4, CD28, ICOS and closely located PD-1, all related to immune activation and considered as promising candidate genes for susceptibility to coeliac disease (CD). We present here the results of a genetic linkage and association analysis of nine markers located in this gene region in a large combined European material of 796 families with CD from Finland, Sweden, Norway, UK, France and Italy. The joint analysis supports earlier findings that this susceptibility locus, assigned as CELIAC3, merits further studies. Nominally significant linkage to CD was found in 314 families including affected sib pairs. Each of the five populations showed weak associations to several marker alleles, but the analysis revealed, however, no conclusive evidence for a primary functional gene or gene variant present in the total set of families. The results suggest that the CD risk due to 2q33 gene region is complex and may involve more than one susceptibility allele, which possibly differ from other autoimmune diseases.
引用
收藏
页码:212 / 222
页数:11
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