Enteral immunotherapy in the treatment of chronic enterocolitis in interleukin-10-deficient mice

Hepatogastroenterology. 2003 May-Jun;50(51):670-5.

Abstract

Background/aims: Transgenic IL-10-deficient mice (IL-10 ko mice) spontaneously develop a chronic inflammatory bowel disease that is reminiscent of Crohn's disease. In a randomized, prospective, comparative study, we evaluated the effect of local, endoluminal immunotherapy by duodenal injection of mouse recombinant IL-10 (rm IL-10), in IL-10 ko mice with chronic enterocolitis; the first of its kind.

Methodology: Sixteen IL-10 ko mice received a monoinjection of rm IL-10 into the duodenum while a control group of 16 IL-10 ko mice received an injection of physiological saline. Histology of the entire bowel and plasma concentrations of IL-4, IL-6, IL-10, tumor necrosis factor-alpha, and interferon-gamma were analyzed on the 3rd or 7th postoperative day.

Results: The histological features of the specimens from IL-10 ko mice were, non-specific, segmentary and located mainly in the ileum. Lesions were of more significance in mice injected with physiological saline than in those receiving IL-10 in the proximal ileum, near to the site of injection. Plasma concentrations of IL-6 were higher in IL-10 ko mice than in the control group.

Conclusions: This study confirms that there is hyperproduction of Th1 cytokines in IL-10 ko mice and also suggests that endoluminal administration of IL-10 may be envisaged for the treatment or prevention of enterocolitis.

MeSH terms

  • Animals
  • Crohn Disease / immunology*
  • Crohn Disease / pathology
  • Disease Models, Animal
  • Duodenum
  • Enterocolitis / immunology*
  • Enterocolitis / pathology
  • Female
  • Ileum / immunology
  • Ileum / pathology
  • Immunotherapy*
  • Injections
  • Interleukin-10 / administration & dosage*
  • Interleukin-10 / deficiency*
  • Interleukin-10 / genetics
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / pathology
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Recombinant Proteins / pharmacology

Substances

  • Recombinant Proteins
  • Interleukin-10