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(American Journal of Pathology. 1998;153:121-130.)
© 1998 American Society for Investigative Pathology


Regular Articles

In Situ Expression of Interleukin-10 in Noninflamed Human Gut and in Inflammatory Bowel Disease

Frank Autschbach* , Jutta Braunstein{dagger} , Burkhard Helmke* , Ivan Zuna{ddagger} , Guido Schürmann§ , Zofia I. Niemir* , Reinhard Wallich{dagger} , Herwart F. Otto* and Stefan C. Meuer{dagger}

From the Institute of Pathology* and Immunology{dagger} and Department of Surgery,§ and the Department of Radiological Diagnostics and Therapy,{ddagger} German Cancer Research Center, Heidelberg, Germany

A dysregulated secretion of contra-inflammatory cytokines such as interleukin-10 (IL-10) could play a role in the pathogenesis of inflammatory bowel disease (IBD). We have investigated the expression of IL-10 in gut tissues from patients with Crohn's disease (CD), ulcerative colitis (UC) and controls by mRNA in situ hybridization and immunohistochemistry. Intestinal epithelial cells were found to express IL-10 mRNA and IL-10 protein in all of the tissues investigated without any major differences in the expression patterns. However, compared with noninflamed gut, significantly increased numbers of mononuclear cells (MNCs) producing IL-10 were present in inflamed gut, both in CD and UC. This cytokine was expressed most prominently by inflammatory infiltrates enriched in macrophages, although T cells seem to contribute to its production as well. Elevated IL-10 expression in IBD was mainly detected in the submucosa, whereas IL-10 production by lamina propria cells remained comparably low. In contrast, the expression of IL-1ß mRNA was preferentially increased in the lamina propria. Our data argue against a general deficiency in IL-10 production in IBD. The results suggest rather that the local production of IL-10 by mucosal MNCs in IBD is insufficient to down-regulate pro-inflammatory cytokines such as IL-1ß in the lamina propria compartment.





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