Cargando…

Expression and role of interleukin-9 in Vogt-Koyanagi-Harada disease

PURPOSE: Vogt-Koyanagi-Harada (VKH) disease is a systemic autoimmune disease that can lead to blindness. This study was designed to investigate whether interleukin (IL)-9 plays a role in the development of VKH disease. METHODS: IL-9, IL-17, and interferon (IFN)-γ levels, present in the supernatants...

Descripción completa

Detalles Bibliográficos
Autores principales: Peng, Zhixi, Jiang, Shaoqiu, Wu, Mingxing, Zhou, Xiyuan, Wang, Qian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5534488/
https://www.ncbi.nlm.nih.gov/pubmed/28761327
_version_ 1783253774421196800
author Peng, Zhixi
Jiang, Shaoqiu
Wu, Mingxing
Zhou, Xiyuan
Wang, Qian
author_facet Peng, Zhixi
Jiang, Shaoqiu
Wu, Mingxing
Zhou, Xiyuan
Wang, Qian
author_sort Peng, Zhixi
collection PubMed
description PURPOSE: Vogt-Koyanagi-Harada (VKH) disease is a systemic autoimmune disease that can lead to blindness. This study was designed to investigate whether interleukin (IL)-9 plays a role in the development of VKH disease. METHODS: IL-9, IL-17, and interferon (IFN)-γ levels, present in the supernatants of cultured peripheral blood mononuclear cells (PBMCs) and CD4+T cells, were assessed with enzyme-linked immunosorbent assay. IL-9 mRNA expression in PBMCs was measured with real-time quantitative PCR. The proliferation of PBMCs in response to different doses of recombinant human IL-9 (rIL-9) was measured using the Cell Counting Kit-8 assay. RESULTS: IL-9 mRNA levels in PBMCs were statistically significantly elevated in patients with active VKH disease compared to those in patients with inactive VKH disease (p<0.05) and normal controls (p<0.05). Statistically significantly higher expression of IL-9 was observed in the supernatants of stimulated PBMCs (p<0.01) and CD4+ T cells (p<0.01) from patients with active VKH disease compared to that in cells from patients with inactive VKH disease and normal controls. rIL-9 at a concentration of 100 ng/ml did not induce proliferation of PBMCs (p>0.05). After the PBMCs and CD4+ T cells were stimulated with rIL-9 (100 ng/ml), the secretion of IL-17 was increased statistically significantly (p<0.05), whereas the level of IFN-γ was not statistically significantly altered (p>0.05). CONCLUSIONS: These findings suggest that IL-9 is involved in the pathogenesis of VKH disease, and that IL-9 might also enhance the inflammatory response by increasing the secretion of IL-17, an established proinflammatory cytokine in VKH disease. Manipulation of IL-9 could represent a novel option for the treatment of VKH disease.
format Online
Article
Text
id pubmed-5534488
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Molecular Vision
record_format MEDLINE/PubMed
spelling pubmed-55344882017-07-31 Expression and role of interleukin-9 in Vogt-Koyanagi-Harada disease Peng, Zhixi Jiang, Shaoqiu Wu, Mingxing Zhou, Xiyuan Wang, Qian Mol Vis Research Article PURPOSE: Vogt-Koyanagi-Harada (VKH) disease is a systemic autoimmune disease that can lead to blindness. This study was designed to investigate whether interleukin (IL)-9 plays a role in the development of VKH disease. METHODS: IL-9, IL-17, and interferon (IFN)-γ levels, present in the supernatants of cultured peripheral blood mononuclear cells (PBMCs) and CD4+T cells, were assessed with enzyme-linked immunosorbent assay. IL-9 mRNA expression in PBMCs was measured with real-time quantitative PCR. The proliferation of PBMCs in response to different doses of recombinant human IL-9 (rIL-9) was measured using the Cell Counting Kit-8 assay. RESULTS: IL-9 mRNA levels in PBMCs were statistically significantly elevated in patients with active VKH disease compared to those in patients with inactive VKH disease (p<0.05) and normal controls (p<0.05). Statistically significantly higher expression of IL-9 was observed in the supernatants of stimulated PBMCs (p<0.01) and CD4+ T cells (p<0.01) from patients with active VKH disease compared to that in cells from patients with inactive VKH disease and normal controls. rIL-9 at a concentration of 100 ng/ml did not induce proliferation of PBMCs (p>0.05). After the PBMCs and CD4+ T cells were stimulated with rIL-9 (100 ng/ml), the secretion of IL-17 was increased statistically significantly (p<0.05), whereas the level of IFN-γ was not statistically significantly altered (p>0.05). CONCLUSIONS: These findings suggest that IL-9 is involved in the pathogenesis of VKH disease, and that IL-9 might also enhance the inflammatory response by increasing the secretion of IL-17, an established proinflammatory cytokine in VKH disease. Manipulation of IL-9 could represent a novel option for the treatment of VKH disease. Molecular Vision 2017-07-31 /pmc/articles/PMC5534488/ /pubmed/28761327 Text en Copyright © 2017 Molecular Vision. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited, used for non-commercial purposes, and is not altered or transformed.
spellingShingle Research Article
Peng, Zhixi
Jiang, Shaoqiu
Wu, Mingxing
Zhou, Xiyuan
Wang, Qian
Expression and role of interleukin-9 in Vogt-Koyanagi-Harada disease
title Expression and role of interleukin-9 in Vogt-Koyanagi-Harada disease
title_full Expression and role of interleukin-9 in Vogt-Koyanagi-Harada disease
title_fullStr Expression and role of interleukin-9 in Vogt-Koyanagi-Harada disease
title_full_unstemmed Expression and role of interleukin-9 in Vogt-Koyanagi-Harada disease
title_short Expression and role of interleukin-9 in Vogt-Koyanagi-Harada disease
title_sort expression and role of interleukin-9 in vogt-koyanagi-harada disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5534488/
https://www.ncbi.nlm.nih.gov/pubmed/28761327
work_keys_str_mv AT pengzhixi expressionandroleofinterleukin9invogtkoyanagiharadadisease
AT jiangshaoqiu expressionandroleofinterleukin9invogtkoyanagiharadadisease
AT wumingxing expressionandroleofinterleukin9invogtkoyanagiharadadisease
AT zhouxiyuan expressionandroleofinterleukin9invogtkoyanagiharadadisease
AT wangqian expressionandroleofinterleukin9invogtkoyanagiharadadisease