Increased frequencies of circulating CXCL10-, CXCL8- and CCL4-producing monocytes and Siglec-3-expressing myeloid dendritic cells in systemic sclerosis patients |
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Authors: | Tiago Carvalheiro Sara Horta Joel A. G. van Roon Mariana Santiago Maria J. Salvador Hélder Trindade Timothy R. D. J. Radstake José A. P. da Silva Artur Paiva |
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Affiliation: | 1.Blood and Transplantation Center of Coimbra,Portuguese Institute of Blood and Transplantation,Coimbra,Portugal;2.Department of Rheumatology and Clinical Immunology,University Medical Center Utrecht,Utrecht,The Netherlands;3.Laboratory of Translational Immunology,University Medical Center Utrecht,Utrecht,The Netherlands;4.Department of Chemistry,University of Aveiro,Aveiro,Portugal;5.Department of Rheumatology,Coimbra University Hospital Center,Coimbra,Portugal;6.Faculty of Medicine,University of Coimbra,Coimbra,Portugal;7.Flow Cytometry Unit, Clinical Pathology Service,Coimbra University Hospital Center,Coimbra,Portugal |
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Abstract: |
ObjectiveTo investigate the ex vivo pro-inflammatory properties of classical and non-classical monocytes as well as myeloid dendritic cells (mDCs) in systemic sclerosis (SSc) patients.MethodsSpontaneous production of CXCL10, CCL4, CXCL8 and IL-6 was intracellularly evaluated in classical, non-classical monocytes and Siglec-3-expressing mDCs from peripheral blood of SSc patients and healthy controls (HC) through flow cytometry. In addition, production of these cytokines was determined upon toll-like receptor (TLR) 4 plus Interferon-γ (IFN-γ) stimulation.ResultsThe frequency of non-classical monocytes spontaneously producing CXCL10 was increased in both limited (lcSSc) and diffuse cutaneous (dcSSC) subsets of SSc patients and CCL4 was augmented in dcSSc patients. The proportion of CCL4-producing mDCs was also elevated in dcSSc patients and the percentage of mDCS producing CXCL10 only in lcSSc patients. Upon stimulation, the frequency of non-classical monocytes expressing CXCL8 was increased in both patient groups and mDCs expressing CXCL8 only in lcSSc. Moreover, these parameters in unsupervised clustering analysis identify a subset of patients which are characterized by lung fibrosis and reduced pulmonary function.ConclusionsThese data point towards a role of activated non-classical monocytes and mDCs producing enhanced levels of proinflammatory cytokines in SSc, potentially contributing to lung fibrosis. |
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