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Pediatric Rheumatology

, 11:P81 | Cite as

PReS-FINAL-2069: T cells secreting granulocyte-macrophage colony stimulating factor (GM-CSF) within the inflammed joint originate from an "EX-Th17" population

  • K Nistala
  • C Piper
  • A Pesenacker
  • D Bending
  • B Thirugnanabalan
  • L Wedderburn
Open Access
Poster presentation
  • 426 Downloads

Keywords

Peripheral Blood Mononuclear Cell Th17 Cell Juvenile Idiopathic Arthritis Human Autoimmune Disease Capture Assay 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Introduction

Since 2003, the established paradigm of T cell immunology has defined interleukin (IL)-17 as a dominant Th17 cell derived cytokine driving autoimmune disease. Recent murine studies have challenged this, identifying GM-CSF as a Th17 related cytokine necessary and sufficient for the induction of autoimmunity. The origin of GM-CSF+ T cells and their relationship with IL-17 secreting cells is unclear in human autoimmune disease. Trials of biologic agents targeting the GM-CSF pathway show promise in rheumatoid arthritis, so it is important to establish if GM-CSF contributes to the inflammatory environment of the arthritic joint in Juvenile Idiopathic Arthritis (JIA).

Objectives

To analyse T cell GM-CSF production in the JIA joint and investigate the origin of GM-CSF+ T cells by testing for co-expression of the Th17 marker CD161 and modelling the plasticity of Th17 cells towards a GM-CSF phenotype in vitro.

Methods

Peripheral blood mononuclear cells (PBMC) and synovial fluid mononuclear cells (SFMC) from 17 patients with JIA were stimulated with PMA and ionomycin in the presence of Brefeldin A and analysed for IL-17, interferon gamma (ifnγ), GM-CSF and CD161 expression by flow cytometry. In some experiments Th17 cells were purified from healthy donor PBMC using a cytokine capture assay and upregulation of GM-CSF was examined after culture, in the presence of IL-12.

Results

SFMC from patients with JIA were enriched for GM-CSF-secreting CD4 T cells, compared to matched PBMC (21% vs 1.7% of CD4 T cells, p = 0.0012). The enrichment was most marked within the synovial CD161+ Th1 cell compartment. Following culture in the presence of IL-12, purified Th17 cells preferentially upregulated GM-CSF compared to IL-17- CD4 T cells (62% vs 35% of CD4 T cells).

Conclusion

GM-CSF secreting T cells are enriched within the JIA joint. Our data shows for the first time that synovial GM-CSF+ T cells demonstrate a phenotype previously associated with ex-Th17 cells, namely IL-17-ifnγ+CD161+. We propose that synovial Th17 cells may drive ongoing local inflammation by undergoing plasticity towards a GM-CSF expressing phenotype in response to elevated synovial IL-12.

Disclosure of interest

None declared.

Copyright information

© Nistala et al.; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 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.

Authors and Affiliations

  • K Nistala
    • 1
  • C Piper
    • 1
  • A Pesenacker
    • 2
  • D Bending
    • 2
  • B Thirugnanabalan
    • 2
  • L Wedderburn
    • 2
  1. 1.Centre for Rheumatology, Division of MedicineUniversity College LondonLondonUK
  2. 2.Rheumatology UnitUCL Institute of Child HealthLondonUK

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