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Serum concentrations of IL-17A, IL-17B, IL-17E and IL-17F in patients with systemic sclerosis
INTRODUCTION: Immune system activation, microvascular abnormalities and extracellular matrix deposition in tissues play roles in systemic sclerosis (SSc). Th17 cells producing interleukin (IL)-17 are involved in the pathogenesis of many autoimmune-mediated inflammatory diseases; however, the role of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524200/ https://www.ncbi.nlm.nih.gov/pubmed/31110538 http://dx.doi.org/10.5114/aoms.2019.84738 |
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author | Robak, Ewa Gerlicz-Kowalczuk, Zofia Dziankowska-Bartkowiak, Bozena Wozniacka, Anna Bogaczewicz, Jaroslaw |
author_facet | Robak, Ewa Gerlicz-Kowalczuk, Zofia Dziankowska-Bartkowiak, Bozena Wozniacka, Anna Bogaczewicz, Jaroslaw |
author_sort | Robak, Ewa |
collection | PubMed |
description | INTRODUCTION: Immune system activation, microvascular abnormalities and extracellular matrix deposition in tissues play roles in systemic sclerosis (SSc). Th17 cells producing interleukin (IL)-17 are involved in the pathogenesis of many autoimmune-mediated inflammatory diseases; however, the role of IL-17 in SSc remains unclear. MATERIAL AND METHODS: The concentrations of IL-17A, IL-17B, IL-17E, and IL-17F in the serum of patients with SSc and in the healthy control group were assessed with regard to type of the disease – whether limited (lSSc) or diffuse (dSSc) – and symptoms. RESULTS: No difference was found between patients with SSc and the control group as regards the serum concentration of IL-17A. However, IL-17B and IL-17E levels in patients with SSc, and its types diffuse and limited were higher (p < 0.001) compared to the control. The serum level of IL-17F was higher in SSc (p < 0.005) and lSSc (p < 0.05) compared to the control. Serum concentration of IL-17B was elevated in SSc patients with renal abnormalities (p < 0.05) compared to those without. Serum levels of IL-17B correlated with the levels of IL-17E in patients with SSc (r = 0.54, p < 0.05). CONCLUSIONS: Increased synthesis of IL-17B, IL-17E and IL-17F appears to play a role in the pathogenesis of SSc, in contrast to IL-17A. Higher levels of IL-17B and IL-17E are associated with the development of both lSSc and dSSc, whereas IL-17F is associated with lSSc only. Further studies are needed to elucidate their role in the pathogenesis of the disease. |
format | Online Article Text |
id | pubmed-6524200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-65242002019-05-20 Serum concentrations of IL-17A, IL-17B, IL-17E and IL-17F in patients with systemic sclerosis Robak, Ewa Gerlicz-Kowalczuk, Zofia Dziankowska-Bartkowiak, Bozena Wozniacka, Anna Bogaczewicz, Jaroslaw Arch Med Sci Clinical Research INTRODUCTION: Immune system activation, microvascular abnormalities and extracellular matrix deposition in tissues play roles in systemic sclerosis (SSc). Th17 cells producing interleukin (IL)-17 are involved in the pathogenesis of many autoimmune-mediated inflammatory diseases; however, the role of IL-17 in SSc remains unclear. MATERIAL AND METHODS: The concentrations of IL-17A, IL-17B, IL-17E, and IL-17F in the serum of patients with SSc and in the healthy control group were assessed with regard to type of the disease – whether limited (lSSc) or diffuse (dSSc) – and symptoms. RESULTS: No difference was found between patients with SSc and the control group as regards the serum concentration of IL-17A. However, IL-17B and IL-17E levels in patients with SSc, and its types diffuse and limited were higher (p < 0.001) compared to the control. The serum level of IL-17F was higher in SSc (p < 0.005) and lSSc (p < 0.05) compared to the control. Serum concentration of IL-17B was elevated in SSc patients with renal abnormalities (p < 0.05) compared to those without. Serum levels of IL-17B correlated with the levels of IL-17E in patients with SSc (r = 0.54, p < 0.05). CONCLUSIONS: Increased synthesis of IL-17B, IL-17E and IL-17F appears to play a role in the pathogenesis of SSc, in contrast to IL-17A. Higher levels of IL-17B and IL-17E are associated with the development of both lSSc and dSSc, whereas IL-17F is associated with lSSc only. Further studies are needed to elucidate their role in the pathogenesis of the disease. Termedia Publishing House 2019-04-30 2019-05 /pmc/articles/PMC6524200/ /pubmed/31110538 http://dx.doi.org/10.5114/aoms.2019.84738 Text en Copyright: © 2019 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Clinical Research Robak, Ewa Gerlicz-Kowalczuk, Zofia Dziankowska-Bartkowiak, Bozena Wozniacka, Anna Bogaczewicz, Jaroslaw Serum concentrations of IL-17A, IL-17B, IL-17E and IL-17F in patients with systemic sclerosis |
title | Serum concentrations of IL-17A, IL-17B, IL-17E and IL-17F in patients with systemic sclerosis |
title_full | Serum concentrations of IL-17A, IL-17B, IL-17E and IL-17F in patients with systemic sclerosis |
title_fullStr | Serum concentrations of IL-17A, IL-17B, IL-17E and IL-17F in patients with systemic sclerosis |
title_full_unstemmed | Serum concentrations of IL-17A, IL-17B, IL-17E and IL-17F in patients with systemic sclerosis |
title_short | Serum concentrations of IL-17A, IL-17B, IL-17E and IL-17F in patients with systemic sclerosis |
title_sort | serum concentrations of il-17a, il-17b, il-17e and il-17f in patients with systemic sclerosis |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524200/ https://www.ncbi.nlm.nih.gov/pubmed/31110538 http://dx.doi.org/10.5114/aoms.2019.84738 |
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