Experimental murine model for autoimmune enterocolitis using Klebsiella pneumoniae O3 lipopolysaccharide as a potent immunological adjuvant.

Abstract

An experimental model for autoimmune enterocolitis was produced in mice by repeated immunization of homologous colon extract together with Klebsiella 03 lipopolysaccharide (KO3 LPS) as an immunological adjuvant. Histological changes in the intestinal lesions were characterized by infiltration with polymorphonuclear leukocytes in the lamina propria, muscularis mucosae and submucosa of repeatedly immunized mice. No such intestinal lesions were produced in mice receiving injections of colon extract alone or KO3 LPS alone. Development of the autoantibody and delayed-type hypersensitivity against colon extract were found in mice immunized with the mixture of colon extract and KO3 LPS. Distinct positive staining was detected specifically on the columnar epithelium of villi. Sera from hyperimmunized mice defined organ-specific antigens present in the intestine. Therefore, it was suggested that the intestinal lesions might be caused by an autoimmune mechanism.

• Authors: N Paeng, A Morikawa, Y Kato, T Sugiyama, N Koide, T Yoshida, T Yokochi
• Journal: Microbiology and immunology (Microbiol Immunol) Vol. 43 Issue 1 Pg. 45-52 ( 1999) ISSN: 0385-5600 [Print] Australia
• PMID: 10100746 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Adjuvants, Immunologic
• Autoantibodies
• Autoantigens
• Klebsiella O3 lipopolysaccharide
• Lipopolysaccharides

Topics

• Adjuvants, Immunologic
• Animals
• Autoantibodies (blood)
• Autoantigens (analysis)
• Autoimmune Diseases (immunology)
• Colon (immunology)
• Disease Models, Animal
• Enterocolitis (immunology)
• Female
• Hypersensitivity, Delayed
• Intestines (pathology)
• Klebsiella pneumoniae (chemistry, immunology)
• Lipopolysaccharides (immunology)
• Male
• Mice