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      Inhibition of dextran sulphate sodium (DSS)-induced colitis in mice by intracolonically administered antibodies against adhesion molecules (endothelial leucocyte adhesion molecule-1 (ELAM-1) or intercellular adhesion molecule-1 (ICAM-1)).

      Clinical and Experimental Immunology
      Animals, Antibodies, Monoclonal, immunology, therapeutic use, Colitis, Ulcerative, chemically induced, pathology, therapy, Dextran Sulfate, antagonists & inhibitors, pharmacology, Disease Models, Animal, Dose-Response Relationship, Drug, E-Selectin, biosynthesis, Female, Immunotherapy, Intercellular Adhesion Molecule-1, Interleukin-1, analysis, Mice, Mice, Inbred BALB C, Peroxidase, metabolism

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          Abstract

          We examined the effect of intracolonic administration of anti-adhesion molecule antibodies on DSS-induced colitis in mice. Immunohistochemical staining in mice with colitis showed increased expression of ELAM-1 and ICAM-1 on endothelial cells of vessels in the lamina propria and submucosa at sites of inflamed lesions. Intracolonic administration of anti-ELAM-1 or anti-ICAM-1 antibody decreased bloody stools, anaemia, and histologically evident damage, as well as myeloperoxidase activity and IL-1beta content. We concluded that adhesion molecule expression is important in the development of DSS-induced colitis in mice and that intracolonic administration of anti-adhesion molecule antibodies, especially anti-ELAM-1 antibody, effectively inhibits the colonic inflammation. Intracolonic administration of anti-adhesion molecule antibodies may show therapeutic promise in ulcerative colitis.

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