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IL-1R8 as Pathoimmunological Marker for Severity of Canine Chronic Enteropathy
Chronic enteropathy (CE) is a severe multifactorial gastrointestinal disease that affects dogs and is driven by poorly characterized inflammatory pathways. Imbalance of pro-inflammatory response regulators, including IL-1R8, may be due to different factors, among which the infection with Helicobacte...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9229266/ https://www.ncbi.nlm.nih.gov/pubmed/35737347 http://dx.doi.org/10.3390/vetsci9060295 |
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author | Riva, Federica Bianchessi, Laura Recordati, Camilla Inglesi, Alessia Castiglioni, Vittoria Turin, Lauretta |
author_facet | Riva, Federica Bianchessi, Laura Recordati, Camilla Inglesi, Alessia Castiglioni, Vittoria Turin, Lauretta |
author_sort | Riva, Federica |
collection | PubMed |
description | Chronic enteropathy (CE) is a severe multifactorial gastrointestinal disease that affects dogs and is driven by poorly characterized inflammatory pathways. Imbalance of pro-inflammatory response regulators, including IL-1R8, may be due to different factors, among which the infection with Helicobacteraceae is known to lead to a vicious circle in which excessive pro-inflammatory signaling and gastrointestinal injury reinforce each other and boost the disease. We investigated the expression of IL-1R8 in large intestine biopsies of dogs with or without clinical signs of CE and with previously assessed enterohepatic Helicobacter spp. colonization status by mean of quantitative real-time PCR. Our study revealed that IL-1R8 is downregulated in both acutely (p = 0.0074) and chronically (p = 0.0159) CE affected dogs compared to healthy controls. The data also showed that IL-1R8 expression tends to decrease with colonization by Helicobacter spp. Interestingly, a negative correlation was detected between the level of expression of IL-1R8 and the severity of macroscopic lesions identified by endoscopy and the crypt hyperplasia score. We further compared the expression levels between males and females and found no statistically significant difference between the two groups. No significant difference was observed in IL-1R8 expression profiles with the age of the animals either. Interestingly, an association was uncovered between IL-1R8 expression level and dog breed. Together, our data advance knowledge on gastrointestinal pathoimmunology in dogs and highlight the potential utilization of IL-1R8 as a diagnostic, prognostic and therapeutic biomarker for canine chronic enteropathy. |
format | Online Article Text |
id | pubmed-9229266 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-92292662022-06-25 IL-1R8 as Pathoimmunological Marker for Severity of Canine Chronic Enteropathy Riva, Federica Bianchessi, Laura Recordati, Camilla Inglesi, Alessia Castiglioni, Vittoria Turin, Lauretta Vet Sci Article Chronic enteropathy (CE) is a severe multifactorial gastrointestinal disease that affects dogs and is driven by poorly characterized inflammatory pathways. Imbalance of pro-inflammatory response regulators, including IL-1R8, may be due to different factors, among which the infection with Helicobacteraceae is known to lead to a vicious circle in which excessive pro-inflammatory signaling and gastrointestinal injury reinforce each other and boost the disease. We investigated the expression of IL-1R8 in large intestine biopsies of dogs with or without clinical signs of CE and with previously assessed enterohepatic Helicobacter spp. colonization status by mean of quantitative real-time PCR. Our study revealed that IL-1R8 is downregulated in both acutely (p = 0.0074) and chronically (p = 0.0159) CE affected dogs compared to healthy controls. The data also showed that IL-1R8 expression tends to decrease with colonization by Helicobacter spp. Interestingly, a negative correlation was detected between the level of expression of IL-1R8 and the severity of macroscopic lesions identified by endoscopy and the crypt hyperplasia score. We further compared the expression levels between males and females and found no statistically significant difference between the two groups. No significant difference was observed in IL-1R8 expression profiles with the age of the animals either. Interestingly, an association was uncovered between IL-1R8 expression level and dog breed. Together, our data advance knowledge on gastrointestinal pathoimmunology in dogs and highlight the potential utilization of IL-1R8 as a diagnostic, prognostic and therapeutic biomarker for canine chronic enteropathy. MDPI 2022-06-14 /pmc/articles/PMC9229266/ /pubmed/35737347 http://dx.doi.org/10.3390/vetsci9060295 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Riva, Federica Bianchessi, Laura Recordati, Camilla Inglesi, Alessia Castiglioni, Vittoria Turin, Lauretta IL-1R8 as Pathoimmunological Marker for Severity of Canine Chronic Enteropathy |
title | IL-1R8 as Pathoimmunological Marker for Severity of Canine Chronic Enteropathy |
title_full | IL-1R8 as Pathoimmunological Marker for Severity of Canine Chronic Enteropathy |
title_fullStr | IL-1R8 as Pathoimmunological Marker for Severity of Canine Chronic Enteropathy |
title_full_unstemmed | IL-1R8 as Pathoimmunological Marker for Severity of Canine Chronic Enteropathy |
title_short | IL-1R8 as Pathoimmunological Marker for Severity of Canine Chronic Enteropathy |
title_sort | il-1r8 as pathoimmunological marker for severity of canine chronic enteropathy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9229266/ https://www.ncbi.nlm.nih.gov/pubmed/35737347 http://dx.doi.org/10.3390/vetsci9060295 |
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