Transcriptional network profile on synovial fluid T cells in psoriatic arthritis
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  • 作者:Ugo Fiocco ; Veronica Martini ; Benedetta Accordi ; Francesco Caso…
  • 关键词:Interleukin ; ; Interleukin ; 23 ; Interleukin ; 6 ; Phosphoproteins ; Psoriatic arthritis ; Th17/Treg cells
  • 刊名:Clinical Rheumatology
  • 出版年:2015
  • 出版时间:September 2015
  • 年:2015
  • 卷:34
  • 期:9
  • 页码:1571-1580
  • 全文大小:1,136 KB
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  • 作者单位:Ugo Fiocco (1)
    Veronica Martini (2)
    Benedetta Accordi (3)
    Francesco Caso (1) (4)
    Luisa Costa (1) (4)
    Francesca Oliviero (1)
    Anna Scanu (1)
    Monica Facco (2)
    Daniele Boso (2)
    Mariele Gatto (1)
    Mara Felicetti (1)
    Paola Frallonardo (1)
    Roberta Ramonda (1)
    Lucia Piva (1)
    Renato Zambello (2)
    Carlo Agostini (2)
    Raffaele Scarpa (4)
    Giuseppe Basso (3)
    Gianpietro Semenzato (2)
    Jean-Michel Dayer (5)
    Leonardo Punzi (1)
    Andrea Doria (1)

    1. Rheumatology Unit, Department of Medicine DIMED, University of Padova, Via Giustiniani, 2, 35128, Padova, Italy
    2. Haematology and Clinical Immunology Branch, University of Padova, Via Giustiniani, 2, 35128, Padova, Italy
    3. Department of Woman and Child Health, University of Padova, Via Giustiniani, 2, 35128, Padova, Italy
    4. Rheumatology Unit, Department of Clinical Medicine and Surgery, University Federico II, via S. Pansini 5, 80131, Naples, Italy
    5. Faculty of Medicine, CMU, CH-1211, Geneva, Switzerland
  • 刊物类别:Medicine
  • 刊物主题:Medicine & Public Health
    Rheumatology
  • 出版者:Springer London
  • ISSN:1434-9949
文摘
The objective of the study was to quantify the transcriptional profile, as the main T cell lineage-transcription factors on synovial fluid (SF) T cells, in relation to SF cytokines and T cell frequencies (%) of psoriatic arthritis (PsA) patients. Reverse phase protein array was employed to identify interleukin (IL)-23Rp19-, FOXP3- and related orphan receptor gamma T (RORγt)- protein and Janus associated tyrosine kinases 1 (JAK1), signal transducer and activator and transcription 1 (STAT1), STAT3 and STAT5 phosphoproteins in total T cell lysates from SF of PsA patients. IL-1β, IL-2, IL-6, IL-21 and interferon (INF)-γ were measured using a multiplex bead immunoassay in SF from PsA patients and peripheral blood (PB) from healthy controls (HC). Frequencies of CD4+CD25?/sup>, CD4+CD25high FOXP3+ and CD4+CD25high CD127low Treg, and either mean fluorescence intensity (MFI) of FOXP3+ on CD4+ Treg or MFI of classic IL-6 receptor (IL-6R) α expression on CD4+CD25?/sup> helper/effector T cells (Th/eff) and Treg cells, were quantified in SF of PsA patients and in PB from HC by flow cytometry (FC). In PsA SF samples, IL-2, IL-21 and IFN-γ were not detectable, whereas IL-6 and IL-1β levels were higher than in SF of non-inflammatory osteoarthritis patients. Higher levels of IL-23R-, FOXP3- and RORγt proteins and JAK1, STAT1, STAT3 and STAT5 were found in total T cells from SF of PsA patients compared with PB from HC. Direct correlations between JAK1 Y1022/Y1023 and STAT5 Y694, and STAT3 Y705 and IL6, were found in SF of PsA patients. Increased proportion of CD4+CD25high FOXP3+ and CD4+CD25high CD127low Treg cells and brighter MFI of IL-6Rα were observed both on CD4+CD25high- and CD4+CD25?/sup> T cells in PsA SF. The study showed a distinctive JAK1/STAT3/STAT5 transcriptional network on T cells in the joint microenvironment, outlining the interplay of IL-6, IL-23, IL-1β and γC cytokines in the polarization and plasticity of Th17 and Treg cells, which might participate in the perpetuation of joint inflammation in PsA patients. Keywords Interleukin-1β Interleukin-23 Interleukin-6 Phosphoproteins Psoriatic arthritis Th17/Treg cells

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