The pathogenesis of coeliac disease

被引:80
作者
Dewar, D
Pereira, SP
Ciclitira, PJ
机构
[1] St Thomas Hosp, Rayne Inst, Dept Gastroenterol, London SE1 7EH, England
[2] UCL, Sch Med, Inst Hepatol, London WC1E 6HX, England
关键词
coeliac disease; pathogenesis; gluten; epitope; HLA-DQ2; tissue transglutaminase;
D O I
10.1016/S1357-2725(03)00239-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Coeliac disease is a chronic enteropathy caused by intolerance to gluten proteins. The true prevalence of this condition is greater than previously thought, with increasing numbers of 'silent' cases being diagnosed. Untreated coeliac disease is associated with significant morbidity and increased mortality. There have been a number of advances in our understanding of the pathogenesis of coeliac disease, in particular the mechanisms whereby gluten epitopes are processed, become modified by tissue transglutaminase (tTG) and then interact with HLA restricted T cells. An improved. understanding of the immune response to gluten is likely to lead to the development of novel strategies for the treatment of coeliac disease. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:17 / 24
页数:8
相关论文
共 25 条
[21]   Specificity of tissue transglutaminase explains cereal toxicity in celiac disease [J].
Vader, LW ;
de Ru, A ;
van der Wal, Y ;
Kooy, YMC ;
Benckhuijsen, W ;
Mearin, ML ;
Drijfhout, JW ;
van Veelen, P ;
Koning, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (05) :643-649
[22]   The gluten response in children with Celiac disease is directed toward multiple gliadin and glutenin peptides [J].
Vader, W ;
Kooy, Y ;
Van Veelen, P ;
De Ru, A ;
Harris, D ;
Benckhuijsen, W ;
Peña, S ;
Mearin, L ;
Drijfhout, JW ;
Koning, F .
GASTROENTEROLOGY, 2002, 122 (07) :1729-1737
[23]   Peptide binding characteristics of the coeliac disease-associated DQ(alpha 1*0501, beta 1*0201) molecule [J].
vandeWal, Y ;
Kooy, YMC ;
Drijfhout, JW ;
Amons, R ;
Koning, F .
IMMUNOGENETICS, 1996, 44 (04) :246-253
[24]   Duration of exposure to gluten and risk for autoimmune disorders in patients with celiac disease [J].
Ventura, A ;
Magazzù, G ;
Greco, L .
GASTROENTEROLOGY, 1999, 117 (02) :297-303
[25]   Targeting of gliadin peptides, CD8, α/β-TCR, and γ/δ-TCR to Golgi complexes and vacuoles within celiac disease enterocytes [J].
Zimmer, KP ;
Naim, H ;
Weber, P ;
Ellis, HJ ;
Ciclitira, PJ .
FASEB JOURNAL, 1998, 12 (13) :1349-1357