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Published on: April 21, 2015
Role of interleukin 1 in inflammatory bowel disease--enhanced production during active disease
M Ligumsky1, P L Simon, F Karmeli
1Department of Gastroenterology, Hadassah University Hospital, Hebrew University Hadassah Medical School, Jerusalem, Israel.
Insights
Interleukin 1 (IL-1) levels are significantly elevated in the colonic mucosa of patients with active inflammatory bowel disease (IBD). This finding suggests IL-1 plays a key role in IBD pathogenesis and that suppressing its production may offer therapeutic benefits.
Area of Science:
- Immunology
- Gastroenterology
- Cytokine research
Background:
- Interleukin 1 (IL-1) is a key cytokine in immune and inflammatory responses.
- IL-1 acts as a dominant mediator and marker of inflammation in experimental colitis.
Purpose of the Study:
- To quantify in vitro the production and release of IL-1 from colonic mucosa in patients with active, untreated inflammatory bowel disease (IBD).
- To compare IL-1 levels in patients with ulcerative colitis and Crohn's disease of the colon against normal controls.
Main Methods:
- Colonic mucosal biopsies were obtained from 17 ulcerative colitis patients, 8 Crohn's disease patients, and 16 controls.
- IL-1 content was measured in fresh mucosa, 24-hour organ cultured mucosa, and culture medium.
- The effect of varying doses of prednisolone on IL-1 release was assessed.
Main Results:
- IL-1 content and release were significantly higher in inflamed mucosa compared to controls.
- A dose-dependent inhibition of IL-1 release was observed with prednisolone treatment.
- These results indicate elevated IL-1 production in active IBD.
Conclusions:
- Colonic mucosal IL-1 is significantly increased in active IBD, suggesting a role in disease pathogenesis.
- Pharmacological suppression of IL-1 production could be a potential therapeutic strategy for IBD.
- Further research into IL-1's role and targeted therapies is warranted.
Abstract:
Interleukin 1 is a polypeptide cytokine produced by various cell types and has been shown to have a major role in inflammatory and immunological responses. In experimental colitis it proved to be a dominant mediator and a reliable marker of inflammation. The aim of the present study was to determine in vitro the extent of production and release of interleukin 1 from colonic mucosa of patients with active untreated inflammatory bowel disease. Colonic mucosal biopsy specimens were obtained during colonoscopy from 17 patients with ulcerative colitis, eight patients with Crohn's disease of the colon, and 16 normal control subjects. Interleukin 1 content was determined in fresh and 24 hour organ cultured mucosa as well as in cultured medium. Interleukin 1 content and release were significantly higher in the inflamed mucosa compared with that of control subjects. Prednisolone inhibited interleukin 1 release in a dose dependent fashion. We conclude that colonic mucosal interleukin 1 content and production is significantly raised in active inflammatory bowel disease and may have a role in the pathogenesis of the inflammatory response. Pharmacological suppression of tissue interleukin 1 production may have a beneficial therapeutic effect.
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