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Ectopic lymphoid neogenesis is strongly associated with activation of the IL-23 pathway in rheumatoid synovitis

INTRODUCTION: The functional relevance of synovial ectopic lymphoid neogenesis (ELN) in rheumatoid arthritis (RA) remains unknown. As ELN correlates with the degree of tissue inflammation, we investigated whether ELN was associated with specific cytokine profiles. METHODS: Synovial ELN was determine...

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Autores principales: Cañete, Juan D., Celis, Raquel, Yeremenko, Nataliya, Sanmartí, Raimon, van Duivenvoorde, Leonie, Ramírez, Julio, Blijdorp, Iris, García-Herrero, Carmen M., Pablos, José L., Baeten, Dominique L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496927/
https://www.ncbi.nlm.nih.gov/pubmed/26156866
http://dx.doi.org/10.1186/s13075-015-0688-0
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author Cañete, Juan D.
Celis, Raquel
Yeremenko, Nataliya
Sanmartí, Raimon
van Duivenvoorde, Leonie
Ramírez, Julio
Blijdorp, Iris
García-Herrero, Carmen M.
Pablos, José L.
Baeten, Dominique L.
author_facet Cañete, Juan D.
Celis, Raquel
Yeremenko, Nataliya
Sanmartí, Raimon
van Duivenvoorde, Leonie
Ramírez, Julio
Blijdorp, Iris
García-Herrero, Carmen M.
Pablos, José L.
Baeten, Dominique L.
author_sort Cañete, Juan D.
collection PubMed
description INTRODUCTION: The functional relevance of synovial ectopic lymphoid neogenesis (ELN) in rheumatoid arthritis (RA) remains unknown. As ELN correlates with the degree of tissue inflammation, we investigated whether ELN was associated with specific cytokine profiles. METHODS: Synovial ELN was determined by immunohistology and long CD21 isoform (CD21L) expression. Cytokine expression was determined by multiplex enzyme-linked immunosorbent assay (ELISA) and quantitative polymerase chain reaction (PCR) as well as immunohistology in synovial fluid (SF) (n = 44) and tissue (ST) (n = 108), respectively. Production of ELN-associated chemokines by fibroblast-like synoviocytes (FLS) was studied in vitro. RESULTS: Screening analysis of SF by multiplex ELISA showed higher protein levels of interleukin (IL)-23 (p = 0.018) and IL-17F (p = 0.028) in ELN+ versus ELN- samples. Other cytokines, including IL-17A, IL-6, and tumor necrosis factor (TNF)-α, were not different. The association between IL-23 and ELN was not biased by disease activity or other clinical features and was confirmed by higher IL-23 mRNA expression in ELN+ versus ELN- ST samples (p = 0.030), a correlation between IL-23 and CD21L expression in the same samples (r = 0.70 p < 0.0001), and a similar correlation in two independent ST sample sets (r = 0.778 p < 0.0001 and r = 0.817 p = 0.011). IL-23 p19 staining was neither restricted nor enhanced in close proximity of ectopic lymphoid follicles, and neither IL-23 nor IL-17A stimulation induced expression of the ELN-associated CC chemokine ligand, CCL21 and CXC chemokine ligand CXCL13, by FLS. Downstream of IL-23, CD21L expression was significantly associated with IL-17F, IL-21, and IL-22, but not IL-17A in two independent ST sample sets. CONCLUSIONS: Synovial ELN in RA is strongly associated with activation of the IL-23 pathway but not with IL-17A. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13075-015-0688-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-44969272015-07-10 Ectopic lymphoid neogenesis is strongly associated with activation of the IL-23 pathway in rheumatoid synovitis Cañete, Juan D. Celis, Raquel Yeremenko, Nataliya Sanmartí, Raimon van Duivenvoorde, Leonie Ramírez, Julio Blijdorp, Iris García-Herrero, Carmen M. Pablos, José L. Baeten, Dominique L. Arthritis Res Ther Research Article INTRODUCTION: The functional relevance of synovial ectopic lymphoid neogenesis (ELN) in rheumatoid arthritis (RA) remains unknown. As ELN correlates with the degree of tissue inflammation, we investigated whether ELN was associated with specific cytokine profiles. METHODS: Synovial ELN was determined by immunohistology and long CD21 isoform (CD21L) expression. Cytokine expression was determined by multiplex enzyme-linked immunosorbent assay (ELISA) and quantitative polymerase chain reaction (PCR) as well as immunohistology in synovial fluid (SF) (n = 44) and tissue (ST) (n = 108), respectively. Production of ELN-associated chemokines by fibroblast-like synoviocytes (FLS) was studied in vitro. RESULTS: Screening analysis of SF by multiplex ELISA showed higher protein levels of interleukin (IL)-23 (p = 0.018) and IL-17F (p = 0.028) in ELN+ versus ELN- samples. Other cytokines, including IL-17A, IL-6, and tumor necrosis factor (TNF)-α, were not different. The association between IL-23 and ELN was not biased by disease activity or other clinical features and was confirmed by higher IL-23 mRNA expression in ELN+ versus ELN- ST samples (p = 0.030), a correlation between IL-23 and CD21L expression in the same samples (r = 0.70 p < 0.0001), and a similar correlation in two independent ST sample sets (r = 0.778 p < 0.0001 and r = 0.817 p = 0.011). IL-23 p19 staining was neither restricted nor enhanced in close proximity of ectopic lymphoid follicles, and neither IL-23 nor IL-17A stimulation induced expression of the ELN-associated CC chemokine ligand, CCL21 and CXC chemokine ligand CXCL13, by FLS. Downstream of IL-23, CD21L expression was significantly associated with IL-17F, IL-21, and IL-22, but not IL-17A in two independent ST sample sets. CONCLUSIONS: Synovial ELN in RA is strongly associated with activation of the IL-23 pathway but not with IL-17A. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13075-015-0688-0) contains supplementary material, which is available to authorized users. BioMed Central 2015-07-09 2015 /pmc/articles/PMC4496927/ /pubmed/26156866 http://dx.doi.org/10.1186/s13075-015-0688-0 Text en © Cañete et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Cañete, Juan D.
Celis, Raquel
Yeremenko, Nataliya
Sanmartí, Raimon
van Duivenvoorde, Leonie
Ramírez, Julio
Blijdorp, Iris
García-Herrero, Carmen M.
Pablos, José L.
Baeten, Dominique L.
Ectopic lymphoid neogenesis is strongly associated with activation of the IL-23 pathway in rheumatoid synovitis
title Ectopic lymphoid neogenesis is strongly associated with activation of the IL-23 pathway in rheumatoid synovitis
title_full Ectopic lymphoid neogenesis is strongly associated with activation of the IL-23 pathway in rheumatoid synovitis
title_fullStr Ectopic lymphoid neogenesis is strongly associated with activation of the IL-23 pathway in rheumatoid synovitis
title_full_unstemmed Ectopic lymphoid neogenesis is strongly associated with activation of the IL-23 pathway in rheumatoid synovitis
title_short Ectopic lymphoid neogenesis is strongly associated with activation of the IL-23 pathway in rheumatoid synovitis
title_sort ectopic lymphoid neogenesis is strongly associated with activation of the il-23 pathway in rheumatoid synovitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496927/
https://www.ncbi.nlm.nih.gov/pubmed/26156866
http://dx.doi.org/10.1186/s13075-015-0688-0
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