Frontiers in Immunology (Feb 2023)
Interleukin 27 is a novel cytokine with anti-inflammatory effects against spondyloarthritis through the suppression of Th17 responses
- Quentin Jouhault,
- Quentin Jouhault,
- Bilade Cherqaoui,
- Bilade Cherqaoui,
- Aude Jobart-Malfait,
- Aude Jobart-Malfait,
- Simon Glatigny,
- Simon Glatigny,
- Marc Lauraine,
- Marc Lauraine,
- Audrey Hulot,
- Audrey Hulot,
- Guillaume Morelle,
- Guillaume Morelle,
- Benjamin Hagege,
- Benjamin Hagege,
- Kétia Ermoza,
- Kétia Ermoza,
- Ahmed El Marjou,
- Brigitte Izac,
- Benjamin Saintpierre,
- Franck Letourneur,
- Séverine Rémy,
- Ignacio Anegon,
- Marie-Christophe Boissier,
- Gilles Chiocchia,
- Gilles Chiocchia,
- Gilles Chiocchia,
- Maxime Breban,
- Maxime Breban,
- Maxime Breban,
- Luiza M. Araujo,
- Luiza M. Araujo
Affiliations
- Quentin Jouhault
- Infection & Inflammation, UMR 1173, Inserm, UVSQ/Université Paris Saclay, Montigny-le-Bretonneux, France
- Quentin Jouhault
- Laboratoire d’Excellence Inflamex, Université Paris-Centre, Paris, France
- Bilade Cherqaoui
- Infection & Inflammation, UMR 1173, Inserm, UVSQ/Université Paris Saclay, Montigny-le-Bretonneux, France
- Bilade Cherqaoui
- Laboratoire d’Excellence Inflamex, Université Paris-Centre, Paris, France
- Aude Jobart-Malfait
- Infection & Inflammation, UMR 1173, Inserm, UVSQ/Université Paris Saclay, Montigny-le-Bretonneux, France
- Aude Jobart-Malfait
- Laboratoire d’Excellence Inflamex, Université Paris-Centre, Paris, France
- Simon Glatigny
- Infection & Inflammation, UMR 1173, Inserm, UVSQ/Université Paris Saclay, Montigny-le-Bretonneux, France
- Simon Glatigny
- Laboratoire d’Excellence Inflamex, Université Paris-Centre, Paris, France
- Marc Lauraine
- Infection & Inflammation, UMR 1173, Inserm, UVSQ/Université Paris Saclay, Montigny-le-Bretonneux, France
- Marc Lauraine
- Laboratoire d’Excellence Inflamex, Université Paris-Centre, Paris, France
- Audrey Hulot
- Infection & Inflammation, UMR 1173, Inserm, UVSQ/Université Paris Saclay, Montigny-le-Bretonneux, France
- Audrey Hulot
- Laboratoire d’Excellence Inflamex, Université Paris-Centre, Paris, France
- Guillaume Morelle
- Infection & Inflammation, UMR 1173, Inserm, UVSQ/Université Paris Saclay, Montigny-le-Bretonneux, France
- Guillaume Morelle
- Laboratoire d’Excellence Inflamex, Université Paris-Centre, Paris, France
- Benjamin Hagege
- Infection & Inflammation, UMR 1173, Inserm, UVSQ/Université Paris Saclay, Montigny-le-Bretonneux, France
- Benjamin Hagege
- Laboratoire d’Excellence Inflamex, Université Paris-Centre, Paris, France
- Kétia Ermoza
- Infection & Inflammation, UMR 1173, Inserm, UVSQ/Université Paris Saclay, Montigny-le-Bretonneux, France
- Kétia Ermoza
- Laboratoire d’Excellence Inflamex, Université Paris-Centre, Paris, France
- Ahmed El Marjou
- Plateforme de production d’anticorps et de protéines recombinantes-Institut Curie/CNRS UMR144, Paris, France
- Brigitte Izac
- Plateforme GenomIC- Université de Paris, Institut Cochin, INSERM-CNRS, Paris, France
- Benjamin Saintpierre
- Plateforme GenomIC- Université de Paris, Institut Cochin, INSERM-CNRS, Paris, France
- Franck Letourneur
- Plateforme GenomIC- Université de Paris, Institut Cochin, INSERM-CNRS, Paris, France
- Séverine Rémy
- Platform Transgenic Rats and ImmunoPhenomics, INSERM UMR 1064-CRTI, Nantes, France
- Ignacio Anegon
- Platform Transgenic Rats and ImmunoPhenomics, INSERM UMR 1064-CRTI, Nantes, France
- Marie-Christophe Boissier
- Inserm UMR1125-Université Sorbonne Paris Nord, Rheumatology Division, Avicenne Hospital (AP-HP), Bobigny, France
- Gilles Chiocchia
- Infection & Inflammation, UMR 1173, Inserm, UVSQ/Université Paris Saclay, Montigny-le-Bretonneux, France
- Gilles Chiocchia
- Laboratoire d’Excellence Inflamex, Université Paris-Centre, Paris, France
- Gilles Chiocchia
- Haematology-Immunology Division, Ambroise Paré Hospital (AP-HP), Boulogne-Billancourt, France
- Maxime Breban
- Infection & Inflammation, UMR 1173, Inserm, UVSQ/Université Paris Saclay, Montigny-le-Bretonneux, France
- Maxime Breban
- Laboratoire d’Excellence Inflamex, Université Paris-Centre, Paris, France
- Maxime Breban
- Rheumatology Division, Ambroise Paré Hospital (AP-HP), Boulogne-Billancourt, France
- Luiza M. Araujo
- Infection & Inflammation, UMR 1173, Inserm, UVSQ/Université Paris Saclay, Montigny-le-Bretonneux, France
- Luiza M. Araujo
- Laboratoire d’Excellence Inflamex, Université Paris-Centre, Paris, France
- DOI
- https://doi.org/10.3389/fimmu.2022.1072420
- Journal volume & issue
-
Vol. 13
Abstract
IntroductionSpondylarthritis (SpA) development in HLA-B27/human β2-microglobulin transgenic rat (B27-rat) is correlated with altered conventional dendritic cell (cDC) function that promotes an inflammatory pattern of CD4+T cells, including a biased expansion of pro-inflammatory Th17 population and imbalance of regulatory T cells cytokine profile. Transcriptomic analysis revealed that cDCs from B27-rats under express IL-27, an anti-inflammatory cytokine which induces the differentiation of IL-10+ regulatory T cells and inhibits Th17 cells.MethodsHere, we first investigated whether in vitro addition of exogenous IL-27 could reverse the inflammatory pattern observed in CD4+ T cells. Next, we performed preclinical assay using IL-27 to investigate whether in vivo treatment could prevent SpA development in B27-rats.Resultsin vitro addition of IL-27 to cocultures of cDCs and CD4+ T cell subsets from B27-rats reduced IL-17 and enhanced IL-10 production by T cells. Likewise, IL-27 inhibited the production of IL-17 by CD4+ T cells from SpA patients. Interestingly, in vivo treatment with recombinant IL-27 starting before SpA onset, inhibited SpA development in B27-rats through the suppression of IL-17/TNF producing CD4+ T cells.DiscussionOverall, our results reveal a potent inhibitory effect of IL-27 and highlight this cytokine as a promising new therapeutic target in SpA, especially for SpA patients non responders to currently approved biotherapies.
Keywords