Probiotic bacteria enhance murine and human intestinal epithelial barrier function

• Published in: Gastroenterology (New York, N.Y. 1943) Vol. 121; no. 3; p. 580
• Main Authors: Madsen, K, Cornish, A, Soper, P, McKaigney, C, Jijon, H, Yachimec, C, Doyle, J, Jewell, L, De Simone, C
• Format: Journal Article
• Language: English
• Published: United States 01.09.2001
• Subjects: Animals; Bifidobacterium; Cell Line; Colitis - metabolism; Colitis - therapy; Epithelial Cells - metabolism; Epithelial Cells - microbiology; Humans; Interleukin-10 - genetics; Interleukin-8 - metabolism; Intestinal Absorption - physiology; Intestinal Mucosa - cytology; Intestinal Mucosa - metabolism; Intestinal Mucosa - microbiology; Lactobacillus; Mice; Mice, Inbred Strains; Mice, Knockout; Patch-Clamp Techniques; Probiotics - pharmacology; Salmonella Infections - prevention & control; Salmonella Infections - therapy; Tumor Necrosis Factor-alpha - metabolism
• ISSN: 0016-5085
• DOI: 10.1053/gast.2001.27224

The probiotic compound, VSL#3, is efficacious as maintenance therapy in pouchitis and ulcerative colitis. The aim of this study was to determine the efficacy of VSL#3 as a primary therapy in the treatment of colitis in the interleukin (IL)-10 gene-deficient mouse. Mechanisms of action of VSL#3 were investigated in T(84) monolayers. IL-10 gene-deficient and control mice received 2.8 x 10(8) colony-forming units per day of VSL#3 for 4 weeks. Colons were removed and analyzed for cytokine production, epithelial barrier function, and inflammation. VSL#3 or conditioned media was applied directly to T(84) monolayers. Treatment of IL-10 gene-deficient mice with VSL#3 resulted in normalization of colonic physiologic function and barrier integrity in conjunction with a reduction in mucosal secretion of tumor necrosis factor alpha and interferon gamma and an improvement in histologic disease. In vitro studies showed that epithelial barrier function and resistance to Salmonella invasion could be enhanced by exposure to a proteinaceous soluble factor secreted by the bacteria found in the VSL#3 compound. Oral administration of VSL#3 was effective as primary therapy in IL-10 gene-deficient mice, and had a direct effect on epithelial barrier function.