Mechanisms of Disease: immunopathogenesis of celiac disease

被引:133
作者
Jabri, Bana [1 ]
Sollid, Ludvig M.
机构
[1] Univ Chicago, Dept Pathol Med & Pediat, Chicago, IL 60637 USA
[2] Univ Oslo, N-0316 Oslo, Norway
[3] Rikshop Univ Hosp, Rikshosp, Radiumhosp Med Ctr, Oslo, Norway
来源
NATURE CLINICAL PRACTICE GASTROENTEROLOGY & HEPATOLOGY | 2006年 / 3卷 / 09期
关键词
celiac disease; gluten; major histocompatibility complex; natural killer receptors; transglutaminase;
D O I
10.1038/ncpgasthep0582
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Celiac disease is a genetic inflammatory disorder with autoimmune components that is induced by the ingestion of dietary gluten. Refractory sprue and enteropathy-associated T-cell lymphoma are rare but distinctive complications of the disease. Although the importance of the adaptive immune response to gluten has been well established, observations now also point towards a central role for the gluten-induced innate stress response in the pathogenesis of celiac disease and its malignant complications.
引用
收藏
页码:516 / 525
页数:10
相关论文
共 79 条
[11]   Identification of tissue transglutaminase as the autoantigen of celiac disease [J].
Dieterich, W ;
Ehnis, T ;
Bauer, M ;
Donner, P ;
Volta, U ;
Riecken, EO ;
Schuppan, D .
NATURE MEDICINE, 1997, 3 (07) :797-801
[12]   Fatal leukemia in interleukin 15 transgenic mice follows early expansions in natural killer and memory phenotype CD8+ T cells [J].
Fehniger, TA ;
Suzuki, K ;
Ponnappan, A ;
VanDeusen, JB ;
Cooper, MA ;
Florea, SM ;
Freud, AG ;
Robinson, ML ;
Durbin, J ;
Caligiuri, MA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (02) :219-231
[13]   INTRAEPITHELIAL LYMPHOCYTE COUNTS IN SMALL INTESTINAL BIOPSIES FROM CHILDREN WITH DIARRHEA [J].
FERGUSON, A ;
MCCLURE, JP ;
TOWNLEY, RRW .
ACTA PAEDIATRICA SCANDINAVICA, 1976, 65 (05) :541-546
[14]   Molecular characterization of covalent complexes between tissue transglutaminase and gliadin peptides [J].
Fleckenstein, B ;
Qiao, SW ;
Larsen, MR ;
Jung, G ;
Roepstorff, P ;
Sollid, LM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (17) :17607-17616
[15]   Gliadin T cell epitope selection by tissue transglutaminase in Celiac disease -: Role of enzyme specificity and pH influence on the transamidation versus deamidation reactions [J].
Fleckenstein, B ;
Molberg, Y ;
Qiao, SW ;
Schmid, DG ;
von der Müllbe, F ;
Elgstoen, K ;
Jung, G ;
Sollid, LM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (37) :34109-34116
[16]   Celiac disease association with CD8+ T cell responses:: Identification of a novel gliadin-derived HLA-A2-restricted epitope [J].
Gianfrani, C ;
Troncone, R ;
Mugione, P ;
Cosentini, E ;
De Pascale, M ;
Faruolo, C ;
Senger, S ;
Terrazzano, G ;
Southwood, S ;
Auricchio, S ;
Sette, A .
JOURNAL OF IMMUNOLOGY, 2003, 170 (05) :2719-2726
[17]   Celiac disease and other precursors to small-bowel malignancy [J].
Green, PHR ;
Jabri, B .
GASTROENTEROLOGY CLINICS OF NORTH AMERICA, 2002, 31 (02) :625-+
[18]   Coeliac disease [J].
Green, PHR ;
Jabri, B .
LANCET, 2003, 362 (9381) :383-391
[19]   A direct role for NKG2D/MICA interaction in villous atrophy during celiac disease [J].
Hüe, S ;
Mention, JJ ;
Monteiro, RC ;
Zhang, SL ;
Cellier, C ;
Schmitz, J ;
Verkarre, V ;
Fodil, N ;
Bahram, S ;
Cerf-Bensussan, N ;
Caillat-Zucman, S .
IMMUNITY, 2004, 21 (03) :367-377
[20]   Lack of association of MYO9B genetic variants with coeliac disease in a British cohort [J].
Hunt, K. A. ;
Monsuur, A. J. ;
McArdle, Wl ;
Kumar, P. J. ;
Travis, S. P. L. ;
Walters, J. R. F. ;
Jewell, D. P. ;
Strachan, D. P. ;
Playford, R. J. ;
Wijmenga, C. ;
van Heel, D. A. .
GUT, 2006, 55 (07) :969-972