Abstract
OBJECTIVE: To 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.
METHODS: Spontaneous 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.
RESULTS: The 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.
CONCLUSIONS: These 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.
Original language | English |
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Pages (from-to) | 169-177 |
Number of pages | 9 |
Journal | Inflammation research : official journal of the European Histamine Research Society ... [et al.] |
Volume | 67 |
Issue number | 2 |
DOIs | |
Publication status | Published - Feb 2018 |
Externally published | Yes |
Keywords
- Adult
- Aged
- Chemokine CCL4/metabolism
- Chemokine CXCL10/metabolism
- Cytokines/biosynthesis
- Dendrites/metabolism
- Female
- Humans
- Interferons/metabolism
- Interleukin-8/metabolism
- Male
- Middle Aged
- Monocytes/metabolism
- Myeloid Cells/metabolism
- Pulmonary Fibrosis/metabolism
- Scleroderma, Systemic/metabolism
- Sialic Acid Binding Ig-like Lectin 1/metabolism
- Toll-Like Receptor 4/metabolism