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10.1186/s13075-018-1652-6

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C6062881!6062881!30053831
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suck abstract from ncbi


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pmid30053831      Arthritis+Res+Ther 2018 ; 20 (ä): ä
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  • Effects of CTLA4-Ig treatment on circulating fibrocytes and skin fibroblasts from the same systemic sclerosis patients: an in vitro assay #MMPMID30053831
  • Cutolo M; Soldano S; Montagna P; Trombetta AC; Contini P; Ruaro B; Sulli A; Scabini S; Stratta E; Paolino S; Pizzorni C; Smith V; Brizzolara R
  • Arthritis Res Ther 2018[]; 20 (ä): ä PMID30053831show ga
  • Background: Systemic sclerosis (SSc) is characterized by vasculopathy and progressive fibrosis. CTLA4-Ig (abatacept) is able to interact with the cell surface costimulatory molecule CD86 and downregulate the target cell. The aim of this study was to evaluate the in-vitro effects of CTLA4-Ig treatment on circulating fibrocytes and skin fibroblasts isolated from the same SSc patient. Methods: Circulating fibrocytes and skin fibroblasts were obtained from eight SSc patients with ?limited? cutaneous involvement and from four healthy subjects (HSs). Samples were analyzed by fluorescence-activated cell sorter analysis (FACS) at baseline (T0) and after 8 days of culture (T8) for CD45, collagen type I (COL I), CXCR4, CD14, CD86, and HLA-DRII expression. Circulating fibrocytes were treated for 3 h and skin fibroblasts for 24/48 h with CTLA4-Ig (10, 50, 100, 500 ?g/ml). Quantitative real-time polymerase chain reaction (qRT-PCR) was performed for CD86, COL I, FN, TGF?, ?SMA, S100A4, CXCR2, CXCR4, CD11a, and Western blotting was performed for COL I and FN. Results: Using qRT-PCR, the T8-cultured SSc circulating fibrocytes which had not been treated with CTLA4-Ig showed higher gene expression for CD86, ?SMA, S100A4, TGF?, and COL I compared with HS circulating fibrocytes. Interestingly, ?SMA/COL I gene expression was significantly lower only in the SSc circulating fibrocytes treated with CTLA4-Ig for 3 h (p 
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