Probiotics and the management of inflammatory bowel disease

被引:132
作者
Fedorak, RN [1 ]
Madsen, KL [1 ]
机构
[1] Univ Alberta, Div Gastroenterol, Edmonton, AB T6G 2C8, Canada
关键词
bifidobacteria; Crohn's disease; inflammatory bowel disease; lactobacilli; pouchitis; probiotics; ulcerative colitis; VSL#3;
D O I
10.1097/00054725-200405000-00018
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The demonstration that immune and epithelial cells can discriminate between different microbial species has extended our understanding of the actions of probiotics beyond simple barrier and antimicrobial concepts. Several probiotic mechanisms of action, relative to inflammatory bowel disease, have been elucidated: (1) competitive exclusion, whereby probiotics compete with microbial pathogens for a limited number of receptors present on the surface epithelium; (2) immunomodulation and/or stimulation of an immune response of gut-associated lymphoid and epithelial cells; (3) antimicrobial activity and suppression of pathogen growth; (4) enhancement of barrier function; and (5) induction of T cell apoptosis in the mucosal immune compartment. The unraveling of these mechanisms of action has led to new support for the use of probiotics in the management of clinical inflammatory bowel disease. Though level I evidence now supports the therapeutic use of probiotics in the treatment of postoperative pouchitis, only levels 2 and 3 evidence is currently available in support of the use of probiotics in the treatment of ulcerative colitis and Crohn's disease. Nevertheless, one significant and consistent finding has emerged during the course of research in the past year: not all probiotic bacteria have similar therapeutic effects. Rigorously designed, controlled clinical trials are vital to investigate the unresolved issues related to efficacy, dose, duration of use, single or multi-strain formulation, and the concomitant use of prebiotics, synbiotics, or antibiotics.
引用
收藏
页码:286 / 299
页数:14
相关论文
共 124 条
[11]   Immunological effects of yogurt addition to a re-nutrition diet in a malnutrition experimental model [J].
Cano, PG ;
Agüero, G ;
Perdigón, G .
JOURNAL OF DAIRY RESEARCH, 2002, 69 (02) :303-316
[12]   Selection of Escherichia coli-inhibiting strains of Lactobacillus paracasei subsp paracasei [J].
Caridi, A .
JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY, 2002, 29 (06) :303-308
[13]  
Chamaillard M, 2003, NAT IMMUNOL, V4, P702, DOI 10.1038/ni945
[14]   LACTOBACILLUS-RHAMNOSUS SEPTICEMIA IN PATIENTS WITH PROLONGED APLASIA RECEIVING CEFTAZIDIME-VANCOMYCIN [J].
CHOMARAT, M ;
ESPINOUSE, D .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1991, 10 (01) :44-44
[15]   Antagonistic activity of Lactobacillus acidophilus LB against intracellular Salmonella enterica serovar typhimurium infecting human enterocyte-like Caco-2/TC-7 cells [J].
Coconnier, MH ;
Liévin, V ;
Lorrot, M ;
Servin, AL .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (03) :1152-1157
[16]   Gastrointestinal effects of prebiotics [J].
Cummings, JH ;
Macfarlane, GT .
BRITISH JOURNAL OF NUTRITION, 2002, 87 :S145-S151
[17]  
Di Marzio L, 2001, NUTR CANCER, V40, P185, DOI 10.1207/S15327914NC402_16
[18]   Production of class II bacteriocins by lactic acid bacteria;: an example of biological warfare and communication [J].
Eijsink, VGH ;
Axelsson, L ;
Diep, DB ;
Håvarstein, LS ;
Holo, H ;
Nes, IF .
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY, 2002, 81 (1-4) :639-654
[19]   Modulation of humoral immune response through probiotic intake [J].
Fang, H ;
Elina, T ;
Heikki, A ;
Seppo, S .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 2000, 29 (01) :47-52
[20]   VSL3 Probiotic mixture induces remission in patients with active ulcerative colitis [J].
Fedorak, RN ;
Gionchetti, P ;
Campieri, M ;
Madsen, K ;
Isaacs, K ;
Desimone, C ;
Sartor, B .
GASTROENTEROLOGY, 2003, 124 (04) :A377-A377