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Imbalance of Th17 and T-regulatory cells in peripheral blood and synovial fluid in treatment naïve children with juvenile idiopathic arthritis

OBJECTIVES: The imbalance between Th17 and T regulatory cells (Tregs) may be a key event in development of autoimmunity. The problem is poorly explored in juvenile idiopathic arthritis (JIA) so far. In this study, peripheral blood (PB) and synovial fluid (SF) Tregs and Th17 cells from were assessed...

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Autores principales: Szymańska-Kałuża, Joanna, Cebula-Obrzut, Barbara, Smolewski, Piotr, Stanczyk, Jerzy, Smolewska, Elżbieta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Polish Society of Experimental and Clinical Immunology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439971/
https://www.ncbi.nlm.nih.gov/pubmed/26155103
http://dx.doi.org/10.5114/ceji.2014.42128
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author Szymańska-Kałuża, Joanna
Cebula-Obrzut, Barbara
Smolewski, Piotr
Stanczyk, Jerzy
Smolewska, Elżbieta
author_facet Szymańska-Kałuża, Joanna
Cebula-Obrzut, Barbara
Smolewski, Piotr
Stanczyk, Jerzy
Smolewska, Elżbieta
author_sort Szymańska-Kałuża, Joanna
collection PubMed
description OBJECTIVES: The imbalance between Th17 and T regulatory cells (Tregs) may be a key event in development of autoimmunity. The problem is poorly explored in juvenile idiopathic arthritis (JIA) so far. In this study, peripheral blood (PB) and synovial fluid (SF) Tregs and Th17 cells from were assessed in untreated JIA children. MATERIAL AND METHODS: In 50 children with JIA the PB or SF percentages of Tregs and Th17 cells were assessed by flow cytometry, in comparison with PB Tregs and Th17 cells from 28 healthy controls. Additionally, in both groups the levels of proinfammatory cytokines, such as interleukin (IL)-1β, IL -6, IL -17, IL -21, IL -23 and tumor necrosis factor α (TN F-α) were assessed using ELI SA method. RESULTS: The proportion of JIA PB Th17 cells was significantly higher than in the controls (p = 0.01). Serum levels of IL -1β, IL -6, IL -17, IL -23 were also significantly higher in JIA (p = 0.011, p = 0.007, p = 0.008 and p = 0.023, respectively). The highest serum IL -6 levels were observed in oligoarthritis JIA (p = 0.031). Synovial fluid IL -21 concentration was distinctly higher in polyarticular JIA. Synovial fluid levels of TN F-α, IL -1β and IL -6 were significantly higher than in JIA PB (p = 0.038, p = 0.013 and p < 0.001, respectively). There was a significant correlation between IL -6 and PB Tregs (p = 0.02). CONCLUSIONS: The results of this comprehensive analysis indicate a role of Th17 cell activation in the pathogenesis of JIA.
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spelling pubmed-44399712015-07-07 Imbalance of Th17 and T-regulatory cells in peripheral blood and synovial fluid in treatment naïve children with juvenile idiopathic arthritis Szymańska-Kałuża, Joanna Cebula-Obrzut, Barbara Smolewski, Piotr Stanczyk, Jerzy Smolewska, Elżbieta Cent Eur J Immunol Original Article OBJECTIVES: The imbalance between Th17 and T regulatory cells (Tregs) may be a key event in development of autoimmunity. The problem is poorly explored in juvenile idiopathic arthritis (JIA) so far. In this study, peripheral blood (PB) and synovial fluid (SF) Tregs and Th17 cells from were assessed in untreated JIA children. MATERIAL AND METHODS: In 50 children with JIA the PB or SF percentages of Tregs and Th17 cells were assessed by flow cytometry, in comparison with PB Tregs and Th17 cells from 28 healthy controls. Additionally, in both groups the levels of proinfammatory cytokines, such as interleukin (IL)-1β, IL -6, IL -17, IL -21, IL -23 and tumor necrosis factor α (TN F-α) were assessed using ELI SA method. RESULTS: The proportion of JIA PB Th17 cells was significantly higher than in the controls (p = 0.01). Serum levels of IL -1β, IL -6, IL -17, IL -23 were also significantly higher in JIA (p = 0.011, p = 0.007, p = 0.008 and p = 0.023, respectively). The highest serum IL -6 levels were observed in oligoarthritis JIA (p = 0.031). Synovial fluid IL -21 concentration was distinctly higher in polyarticular JIA. Synovial fluid levels of TN F-α, IL -1β and IL -6 were significantly higher than in JIA PB (p = 0.038, p = 0.013 and p < 0.001, respectively). There was a significant correlation between IL -6 and PB Tregs (p = 0.02). CONCLUSIONS: The results of this comprehensive analysis indicate a role of Th17 cell activation in the pathogenesis of JIA. Polish Society of Experimental and Clinical Immunology 2014-04-17 2014 /pmc/articles/PMC4439971/ /pubmed/26155103 http://dx.doi.org/10.5114/ceji.2014.42128 Text en Copyright © Central European Journal of Immunology 2014 http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Szymańska-Kałuża, Joanna
Cebula-Obrzut, Barbara
Smolewski, Piotr
Stanczyk, Jerzy
Smolewska, Elżbieta
Imbalance of Th17 and T-regulatory cells in peripheral blood and synovial fluid in treatment naïve children with juvenile idiopathic arthritis
title Imbalance of Th17 and T-regulatory cells in peripheral blood and synovial fluid in treatment naïve children with juvenile idiopathic arthritis
title_full Imbalance of Th17 and T-regulatory cells in peripheral blood and synovial fluid in treatment naïve children with juvenile idiopathic arthritis
title_fullStr Imbalance of Th17 and T-regulatory cells in peripheral blood and synovial fluid in treatment naïve children with juvenile idiopathic arthritis
title_full_unstemmed Imbalance of Th17 and T-regulatory cells in peripheral blood and synovial fluid in treatment naïve children with juvenile idiopathic arthritis
title_short Imbalance of Th17 and T-regulatory cells in peripheral blood and synovial fluid in treatment naïve children with juvenile idiopathic arthritis
title_sort imbalance of th17 and t-regulatory cells in peripheral blood and synovial fluid in treatment naïve children with juvenile idiopathic arthritis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439971/
https://www.ncbi.nlm.nih.gov/pubmed/26155103
http://dx.doi.org/10.5114/ceji.2014.42128
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