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Functional and phenotypical analysis of IL‐6‐secreting CD4+ T cells in human adipose tissue.

Authors :
de Jong, Anja J.
Pollastro, Sabrina
Kwekkeboom, Joanneke C.
Andersen, Stefan N.
Dorjée, Annemarie L.
Bakker, Aleida M.
Alzaid, Fawaz
Soprani, Antoine
Nelissen, Rob G. H. H.
Mullers, Jan B.
Venteclef, Nicolas
de Vries, Niek
Kloppenburg, Margreet
Toes, René E. M.
Ioan‐Facsinay, Andreea
Source :
European Journal of Immunology; Mar2018, Vol. 48 Issue 3, p471-481, 11p
Publication Year :
2018

Abstract

Abstract: Emerging evidence indicates that a dynamic interplay between the immune system and adipocytes contributes to the disturbed homeostasis in adipose tissue of obese subjects. Recently, we observed IL‐6‐secretion by CD4<superscript>+</superscript> T cells from the stromal vascular fraction (SVF) of the infrapatellar fat pad (IFP) of knee osteoarthritis patients directly ex vivo. Here we show that human IL‐6<superscript>+</superscript>CD4<superscript>+</superscript> T cells from SVF display a more activated phenotype than the IL‐6<superscript>−</superscript> T cells, as evidenced by the expression of the activation marker CD69. Analysis of cytokines secretion, as well as expression of chemokine receptors and transcription factors associated with different Th subsets (Treg, Th1, Th2, Th17 and Tfh) revealed that IL‐6‐secreting CD4<superscript>+</superscript> T cells cannot be assigned to a conventional Th subset. TCRβ gene analysis revealed that IL‐6<superscript>+</superscript> and IL‐6<superscript>−</superscript>CD4<superscript>+</superscript> T cells appear clonally unrelated to each other, suggesting a different specificity of these cells. In line with these observations, adipocytes are capable of enhancing IL‐6 production by CD4<superscript>+</superscript> T cells. Thus, IL‐6<superscript>+</superscript>CD4<superscript>+</superscript> T cells are TCRαβ T cells expressing an activated phenotype potentially resulting from an interplay with adipocytes that could be involved in the inflammatory processes in the OA joint. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00142980
Volume :
48
Issue :
3
Database :
Complementary Index
Journal :
European Journal of Immunology
Publication Type :
Academic Journal
Accession number :
128398620
Full Text :
https://doi.org/10.1002/eji.201747037