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(American Journal of Pathology. 1999;155:331-336.)
© 1999 American Society for Investigative Pathology


Short Communication

Increased Expression of IP-10, IL-8, MCP-1, and MCP-3 in Ulcerative Colitis

Mariagrazia Uguccioni*, Paolo Gionchetti{dagger}, Davide F. Robbiani*, Fernando Rizzello{dagger}, Sabrina Peruzzo{dagger}, Massimo Campieri{dagger} and Marco Baggiolini*

From the Theodor Kocher Institute,*
University of Bern, Bern, Switzerland; and the Department of Internal Medicine and Gastroenterology,{dagger}
University of Bologna, Bologna, Italy

Chemokines are thought to be important for the recruitment of granulocytes and mononuclear cells and thus for the maintenance of inflammation in ulcerative colitis (UC). We have studied the expression of interferon-{gamma} inducible protein-10 (IP-10), interleukin-8 (IL-8), monocyte chemoattractant protein (MCP)-1, MCP-3, and macrophage inflammatory protein (MIP)-1{alpha} in UC patients and control individuals to assess the role of these chemokines in disease progression. Colonic biopsies were taken endoscopically from patients and controls, frozen immediately and subsequently stained for IP-10, IL-8, MCP-1, MCP-3, and MIP-1{alpha} in serial sections. Cells infiltrating the lamina propria but not epithelial cells express the analyzed chemokines. They were differentiated and counted, and chemokine-expressing cells were quantified by image analysis. The percentage of cells expressing IP-10, IL-8, MCP-1, and MCP-3 was significantly enhanced in all UC samples as compared to controls. Expression in the controls was borderline, except for IP-10. No expression of MIP-1{alpha} was found in controls and UC. IP-10 was also markedly expressed in the mucosa of control biopsies and therefore could have a role in activated T lymphocytes' recruitment into the healthy mucosa.





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