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Prostaglandin I2 analogues enhance already exuberant Th17 cell responses in systemic sclerosis
  1. Marie-Elise Truchetet1,
  2. Yannick Allanore2,
  3. Elisa Montanari1,
  4. Carlo Chizzolini1,
  5. Nicolò Costantino Brembilla1
  1. 1Division of Immunology and Allergy, University Hospital and School of Medicine, Geneva, Switzerland
  2. 2Rheumatology A department, INSERM U1016 and CNRS, Paris Descartes University, Cochin Hospital, Sorbonne Paris Cité, Paris, France
  1. Correspondence to Dr Carlo Chizzolini, Immunology and Allergy, University Hospital, Rue Gabrielle Perret-Gentil 4, 1211 Geneva 14, Switzerland; carlo.chizzolini{at}


Objective Among pleiotropic effects, the capacity of prostaglandin I2 (PGI2) analogues to affect adaptive immunity remains poorly characterised. The purpose of this study was to assess whether PGI2 analogues could affect T helper (Th) cell responses in patients with systemic sclerosis (SSc) and healthy donors (HD).

Methods Peripheral blood mononuclear cells (PBMC) were obtained from 33 patients with SSc and 29 HD. Cytokine levels in PBMC and monocyte/CD4 T cell cultures were quantified by immunoassays. The frequencies of interleukin (IL)-17A, IL-22, interferon γ (IFNγ) and IL-4-producing CD4 T cells were assessed by multiparametric flow cytometry. Selective receptor antagonists, cytokine blocking antibodies and signalling protein inhibitors were used to identify the receptors and signalling pathways mediating PGI2 analogue effects.

Results Th17 and Th22 cells were more abundant in individuals with SSc than in HD. PGI2 analogues (iloprost, treprostinil and beraprost) significantly increased IL-17A and IL-22 in vitro while decreasing IFNγ production both in SSc and HD PBMC. These effects relied on the specific expansion of Th17 and Th22 and inhibition of Th1 cells. The enhanced Th17 cell responses depended on increased IL-23 production by monocytes, involved the IP prostacyclin receptor and required protein kinase A activation. Importantly, in vivo administration of iloprost in individuals with SSc presenting with digital ulcers resulted in a significant increase in the frequency of Th17 cells.

Conclusions These findings demonstrate that PGI2 analogues affect Th cell differentiation/expansion programmes, favouring Th17 and inhibiting Th1 cell responses in SSc. The impact of these changes on the disease course needs to be taken into consideration and further exploited to improve SSc.

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