Mechanisms of natural tolerance in the intestine - Implications for inflammatory bowel disease

被引:64
作者
Jump, RL
Levine, AD
机构
[1] Case Western Reserve Univ, Sch Med, Dept Med, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Sch Med, Dept Pathol, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Sch Med, Dept Pharmacol, Cleveland, OH 44106 USA
关键词
adaptive immunity; commensal flora; Crohn's disease; innate immunity; intestinal epithelial cell; lymphocyte; review; tolerance; ulcerative colitis;
D O I
10.1097/00054725-200407000-00023
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Tolerance, the regulated inability to respond to a specific immunologic stimulant, is a physiological event important to normal immune function. Just as loss of tolerance to self-proteins results in autoimmune diseases, we assert that loss of tolerance to commensal flora in the intestinal lumen leads to inflammatory bowel disease (1131)). Mechanisms through which the mucosal immune system establishes and remains hyporesponsive toward the presence of food proteins and commensal flora, which we define as natural tolerance, are discussed. In addition to the contributions by commensal flora, the innate host defense and the adaptive immune systems promote natural tolerance to sustain normal mucosal homeostasis. Understanding the molecular and cellular events that mediate natural tolerance will lead to more advanced insights into 1131) pathogenesis and improved therapeutic options.
引用
收藏
页码:462 / 478
页数:17
相关论文
共 204 条
[61]   Oral tolerance [J].
Garside, P ;
Mowat, AM .
SEMINARS IN IMMUNOLOGY, 2001, 13 (03) :177-185
[62]  
Gaskins H.R., 1997, GASTROINTEST MICROBI, V2, P537, DOI DOI 10.1007/978-1-4757-0322-1_14
[63]   Cutting edge: Bacterial flagellin activates basolaterally expressed TLR5 to induce epithelial proinflammatory gene expression [J].
Gewirtz, AT ;
Navas, TA ;
Lyons, S ;
Godowski, PJ ;
Madara, JL .
JOURNAL OF IMMUNOLOGY, 2001, 167 (04) :1882-1885
[64]   Probiotics in infective diarrhoea and inflammatory bowel diseases [J].
Gionchetti, P ;
Rizzello, F ;
Venturi, A ;
Campieri, M .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2000, 15 (05) :489-493
[65]  
Gonsky R, 1998, J IMMUNOL, V160, P4914
[66]  
GOODACRE RL, 1982, GASTROENTEROLOGY, V82, P653
[67]   A CD4(+) T-cell subset inhibits antigen-specific T-cell responses and prevents colitis [J].
Groux, H ;
OGarra, A ;
Bigler, M ;
Rouleau, M ;
Antonenko, S ;
deVries, JE ;
Roncarolo, MG .
NATURE, 1997, 389 (6652) :737-742
[68]   Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p [J].
Hampe, J ;
Frenzel, H ;
Mirza, MM ;
Croucher, PJP ;
Cuthbert, A ;
Mascheretti, S ;
Huse, K ;
Platzer, M ;
Bridger, S ;
Meyer, B ;
Nürnberg, P ;
Stokkers, P ;
Krawczak, M ;
Mathew, CG ;
Curran, M ;
Schreiber, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (01) :321-326
[69]   The role of small intestinal antigen-presenting cells in the induction of T-cell reactivity to soluble protein antigens: Association between aberrant presentation in the lamina propria and oral tolerance [J].
Harper, HM ;
Cochrane, L ;
Williams, NA .
IMMUNOLOGY, 1996, 89 (03) :449-456
[70]   Innate mechanisms of epithelial host defense: spotlight on intestine [J].
Hecht, G .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1999, 277 (03) :C351-C358