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Increased gut permeability and intestinal inflammation precede arthritis onset in the adjuvant-induced model of arthritis

BACKGROUND: Intestinal inflammation, dysbiosis, intestinal permeability (IP), and bacterial translocation (BT) have been identified in patients with spondyloarthritis but the time at which they appear and their contribution to the pathogenesis of the disease is still a matter of debate. OBJECTIVES:...

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Autores principales: Hecquet, Sophie, Totoson, Perle, Martin, Hélène, Algros, Marie-Paule, Saas, Philippe, Pais-de-Barros, Jean-Paul, Atchon, Alban, Valot, Benoît, Hocquet, Didier, Tournier, Maude, Prati, Clément, Wendling, Daniel, Demougeot, Céline, Verhoeven, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242991/
https://www.ncbi.nlm.nih.gov/pubmed/37280714
http://dx.doi.org/10.1186/s13075-023-03069-9
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author Hecquet, Sophie
Totoson, Perle
Martin, Hélène
Algros, Marie-Paule
Saas, Philippe
Pais-de-Barros, Jean-Paul
Atchon, Alban
Valot, Benoît
Hocquet, Didier
Tournier, Maude
Prati, Clément
Wendling, Daniel
Demougeot, Céline
Verhoeven, Frank
author_facet Hecquet, Sophie
Totoson, Perle
Martin, Hélène
Algros, Marie-Paule
Saas, Philippe
Pais-de-Barros, Jean-Paul
Atchon, Alban
Valot, Benoît
Hocquet, Didier
Tournier, Maude
Prati, Clément
Wendling, Daniel
Demougeot, Céline
Verhoeven, Frank
author_sort Hecquet, Sophie
collection PubMed
description BACKGROUND: Intestinal inflammation, dysbiosis, intestinal permeability (IP), and bacterial translocation (BT) have been identified in patients with spondyloarthritis but the time at which they appear and their contribution to the pathogenesis of the disease is still a matter of debate. OBJECTIVES: To study the time-course of intestinal inflammation (I-Inf), IP, microbiota modification BT in a rat model of reactive arthritis, the adjuvant-induced arthritis model (AIA). METHODS: Analysis was performed at 3 phases of arthritis in control and AIA rats: preclinical phase (day 4), onset phase (day 11), and acute phase (day 28). IP was assessed by measuring levels of zonulin and ileal mRNA expression of zonulin. I-inf was assessed by lymphocyte count from rat ileum and by measuring ileal mRNA expression of proinflammatory cytokines. The integrity of the intestinal barrier was evaluated by levels of iFABP. BT and gut microbiota were assessed by LPS, soluble CD14 levels, and 16S RNA sequencing in mesenteric lymph node and by 16S rRNA sequencing in stool, respectively. RESULTS: Plasma zonulin levels increased at the preclinical and onset phase in the AIA group. Plasma levels of iFABP were increased in AIA rats at all stages of the arthritis course. The preclinical phase was characterized by a transient dysbiosis and increased mRNA ileal expression of IL-8, IL-33, and IL-17. At the onset phase, TNF-α, IL-23p19, and IL-8 mRNA expression were increased. No changes in cytokines mRNA expression were observed at the acute phase. Increased CD4(+) and CD8(+) T cell number was measured in the AIA ileum at day 4 and day 11. No increase in BT was observed. CONCLUSION: These data show that intestinal changes precede the development of arthritis but argue against a strict “correlative” model in which arthritis and gut changes are inseparable. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-023-03069-9.
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spelling pubmed-102429912023-06-07 Increased gut permeability and intestinal inflammation precede arthritis onset in the adjuvant-induced model of arthritis Hecquet, Sophie Totoson, Perle Martin, Hélène Algros, Marie-Paule Saas, Philippe Pais-de-Barros, Jean-Paul Atchon, Alban Valot, Benoît Hocquet, Didier Tournier, Maude Prati, Clément Wendling, Daniel Demougeot, Céline Verhoeven, Frank Arthritis Res Ther Research BACKGROUND: Intestinal inflammation, dysbiosis, intestinal permeability (IP), and bacterial translocation (BT) have been identified in patients with spondyloarthritis but the time at which they appear and their contribution to the pathogenesis of the disease is still a matter of debate. OBJECTIVES: To study the time-course of intestinal inflammation (I-Inf), IP, microbiota modification BT in a rat model of reactive arthritis, the adjuvant-induced arthritis model (AIA). METHODS: Analysis was performed at 3 phases of arthritis in control and AIA rats: preclinical phase (day 4), onset phase (day 11), and acute phase (day 28). IP was assessed by measuring levels of zonulin and ileal mRNA expression of zonulin. I-inf was assessed by lymphocyte count from rat ileum and by measuring ileal mRNA expression of proinflammatory cytokines. The integrity of the intestinal barrier was evaluated by levels of iFABP. BT and gut microbiota were assessed by LPS, soluble CD14 levels, and 16S RNA sequencing in mesenteric lymph node and by 16S rRNA sequencing in stool, respectively. RESULTS: Plasma zonulin levels increased at the preclinical and onset phase in the AIA group. Plasma levels of iFABP were increased in AIA rats at all stages of the arthritis course. The preclinical phase was characterized by a transient dysbiosis and increased mRNA ileal expression of IL-8, IL-33, and IL-17. At the onset phase, TNF-α, IL-23p19, and IL-8 mRNA expression were increased. No changes in cytokines mRNA expression were observed at the acute phase. Increased CD4(+) and CD8(+) T cell number was measured in the AIA ileum at day 4 and day 11. No increase in BT was observed. CONCLUSION: These data show that intestinal changes precede the development of arthritis but argue against a strict “correlative” model in which arthritis and gut changes are inseparable. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-023-03069-9. BioMed Central 2023-06-06 2023 /pmc/articles/PMC10242991/ /pubmed/37280714 http://dx.doi.org/10.1186/s13075-023-03069-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Hecquet, Sophie
Totoson, Perle
Martin, Hélène
Algros, Marie-Paule
Saas, Philippe
Pais-de-Barros, Jean-Paul
Atchon, Alban
Valot, Benoît
Hocquet, Didier
Tournier, Maude
Prati, Clément
Wendling, Daniel
Demougeot, Céline
Verhoeven, Frank
Increased gut permeability and intestinal inflammation precede arthritis onset in the adjuvant-induced model of arthritis
title Increased gut permeability and intestinal inflammation precede arthritis onset in the adjuvant-induced model of arthritis
title_full Increased gut permeability and intestinal inflammation precede arthritis onset in the adjuvant-induced model of arthritis
title_fullStr Increased gut permeability and intestinal inflammation precede arthritis onset in the adjuvant-induced model of arthritis
title_full_unstemmed Increased gut permeability and intestinal inflammation precede arthritis onset in the adjuvant-induced model of arthritis
title_short Increased gut permeability and intestinal inflammation precede arthritis onset in the adjuvant-induced model of arthritis
title_sort increased gut permeability and intestinal inflammation precede arthritis onset in the adjuvant-induced model of arthritis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242991/
https://www.ncbi.nlm.nih.gov/pubmed/37280714
http://dx.doi.org/10.1186/s13075-023-03069-9
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