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Peer-reviewed veterinary case report

Toll-like receptor changes in dogs with chronic diarrhea

By Burgener, I A et al.·Published in Journal of veterinary internal medicine·2008·Department of Clinical Veterinary Medicine·View original on PubMed

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Original publication title: Upregulation of toll-like receptors in chronic enteropathies in dogs.

Species:
dog

Plain-English summary

A group of dogs with chronic diarrhea, including some with inflammatory bowel disease (IBD), were studied to understand the role of certain immune receptors in their condition. Researchers found that these receptors, which help the immune system respond to bacteria, were more active in the dogs with IBD compared to healthy dogs. Even though the dogs showed clinical improvement after treatment, the levels of these receptors did not change significantly, suggesting that genetics might play a role in IBD. Most dogs in the study improved with standard therapy, indicating that treatment can be effective for managing their symptoms.

People also search for: dog chronic diarrhea treatment · inflammatory bowel disease in dogs · dog immune system receptors IBD

Abstract

BACKGROUND: Inflammatory bowel disease (IBD) is thought to result from a dysregulated interaction between the host immune system and commensal microflora. Toll-like receptors (TLRs) recognize microbe-associated molecular patterns (MAMPs), but their role in enteropathies in dogs is unknown. HYPOTHESIS: That there is a dysregulation of TLRs recognizing bacterial MAMPs in dogs with IBD. ANIMALS: Sixteen healthy beagles and 12 dogs with steroid-treated (ST) and 23 dogs with food-responsive (FR) diarrhea. METHODS: Prospective, observational study. mRNA expression of canine TLR2, 4, and 9 was evaluated by quantitative real-time RT-PCR in duodenal and colonic biopsies obtained before and after standard therapy. Samples from control dogs were taken at necropsy, with additional biopsies of stomach, jejunum, ileum, and mesenteric lymph node in 6 dogs. RESULTS: There were significant differences (P< or = .017) in expression of TLR2, 4, and 9 between the 6 sampled locations in healthy control dogs (lymph node > small intestine > or = colon). Before therapy, ST expressed more mRNA than control dogs for all 3 receptors (P < .05). There were no significant differences between pretreatment and posttreatment values, even though 32/35 dogs improved clinically. No associations were found when comparing receptor mRNA expression with either histology or clinical activity scores. CONCLUSIONS AND CLINICAL IMPORTANCE: Bacteria-responsive TLR2, 4, and 9 are upregulated in duodenal and colonic mucosa in IBD. This might lead to increased inflammation through interaction with the commensal flora. The absence of significant changes after therapy despite clinical improvement might point toward the existence of a genetic predisposition to IBD as described in human IBD.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/18466244/