Discovering the cause of inflammatory bowel disease: lessons from animal models

被引:17
作者
Arseneau, KO [1 ]
Pizarro, TT [1 ]
Cominelli, F [1 ]
机构
[1] Univ Virginia, Div Gastroenterol & Hepatol, Charlottesville, VA 22906 USA
关键词
D O I
10.1097/00001574-200007000-00004
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The precise cause of inflammatory bowel disease remains unclear. Relevant animal models are important toots for studying the underlying mechanisms of inflammation and disease pathogenesis. The purpose of this review is to summarize the various types of animal models available for use in inflammatory bowel disease research and to illustrate how these models have contributed to a better understanding of the etiopathogenesis of inflammatory bowel disease, particularly focusing on papers published during calendar year 1999. Studies using appropriate animal models have provided important discoveries in this field of investigation. These include determination of the key role that pathogenic and regulatory T cells, proinflammatory and immunoregulatory cytokines, indigenous bacterial flora, and putative predisposing genes play in the disease process. The availability of new animal models that closely resemble the human disease is expected to allow further characterization of the initiating event(s) in inflammatory bowel disease and lead to a possible cure for this devastating disease. Curr Opin Gastroenterol 2000. 16:310-317 (C) 2000 Lippincott Williams & Wilkins, Inc.
引用
收藏
页码:310 / 317
页数:8
相关论文
共 65 条
[31]   Lactobacillus species prevents colitis in interleukin 10 gene-deficient mice [J].
Madsen, KL ;
Doyle, JS ;
Jewell, LD ;
Tavernini, MM ;
Fedorak, RN .
GASTROENTEROLOGY, 1999, 116 (05) :1107-1114
[32]  
Marguerat S, 1999, J IMMUNOL, V163, P4033
[33]  
Martinsson T, 1999, J PHARMACOL EXP THER, V291, P642
[34]   Inflammatory bowel disease-like enteritis and caecitis in a senescence accelerated mouse P1/Yit strain [J].
Matsumoto, S ;
Okabe, Y ;
Setoyama, H ;
Takayama, K ;
Ohtsuka, J ;
Funahashi, H ;
Imaoka, A ;
Okada, Y ;
Umesaki, Y .
GUT, 1998, 43 (01) :71-78
[35]   Intestinal inflammation in adhesion molecule-deficient mice: an assessment of P-selectin alone and in combination with ICAM-1 or E-selectin [J].
McCafferty, DM ;
Smith, CW ;
Granger, DN ;
Kubes, P .
JOURNAL OF LEUKOCYTE BIOLOGY, 1999, 66 (01) :67-74
[36]   Characterization of the mucosal cell-mediated immune response in IL-2 knockout mice before and after the onset of colitis [J].
McDonald, SAC ;
Palmen, MJHJ ;
VanRees, EP ;
MacDonald, TT .
IMMUNOLOGY, 1997, 91 (01) :73-80
[37]  
Miceli R, 1999, J PHARMACOL EXP THER, V290, P464
[38]   Cytokine imbalance and autoantibody production in T cell receptor-alpha mutant mice with inflammatory bowel disease [J].
Mizoguchi, A ;
Mizoguchi, E ;
Chiba, C ;
Spiekermann, GM ;
Tonegawa, S ;
NaglerAnderson, C ;
Bhan, AK .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (03) :847-856
[39]  
Murthy S, 1999, ALIMENT PHARM THER, V13, P251
[40]   ANTIBODIES TO INTERLEUKIN-12 ABROGATE ESTABLISHED EXPERIMENTAL COLITIS IN MICE [J].
NEURATH, MF ;
FUSS, I ;
KELSALL, BL ;
STUBER, E ;
STROBER, W .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (05) :1281-1290