Abstract

Background: Dendritic cells (DCs) are professional antigen-presenting cells (APCs), which play important role in immune responses. DCs are a heterogeneous population and can be divided into groups: myeloid (mDCs) and plasmacytoid (pDCs). Furthemore, DCs are important in rheumatoid arthritis (RA) pathogenesis through antigen presentation and activation autoreactive T-lymphocytes. As established the different subpopulation DCs can promote different immune reactions. That’s why, it may be possible to consider them as a potential target for the development of new target of the immunopathological disorders therapy. Objectives: To investigate the subpopulations of peripheral blood DCs (myeloid and plasmacytoid) in patients with early RA as a predictor of responsibility to disease-modifying antirheumatic drugs (DMARDs) treatment. Methods: Forty nine patients with early RA (duration of the disease up to 12 months) were included in the study. All patients fullfield ACR/EULAR criteria (2010) and received methotrexate, leflunomide, sulfasalazine or their combination. Forty three patients with osteoarthritis (OA) used as a control group. Analysis of the content of the B-lymphocytes, myeloid and plasmacytoid DCs, labeled by antibodies against surface markers, was carried out by flow cytometry. B-lymphocytes, subtypes of peripheral blood DCs were characterized by the following phenotypes: myeloid DCs (CD3-CD14-CD19-HLA-DR + CD11c + CD123-), plasmacytoid DCs (CD3-CD14-CD19-HLA-DR + CD11c-CD123 +), B-lymphocytes (CD19 +). Analysis were performed before treatment and after 3 and 6 months. Results: Patients with early RA are characterized by significant evaluation of the population of plasmacytoid DCs in comparison of patients with moderate stages of rheumatoid arthritis and osteoarthritis (3.8 vs2.1 vs 1, p=0.0042). Furthermore, the difference was found in the number of cells with the phenotype B-lymphocytes: 7.95 * 106/l vs. 3.6* 106/l, respectively (p = 0.014). No significant differences were observed in the number of myeloid DCs. After 6 month of observation we detected reducing amount of plasmacytoid DCs (3.8 before treatment and 2.1 in 6 month, p=0.002) and B-cells that correlated with activity of disease. Conclusion: The data obtained indicated that plasmacytoid DCs are predominant in patients with inflammatory arthritis especially in early RA and correlate with activity of disease that can use as a predictor of good response on DMARDs treatment. Disclosure of Interests: None declared

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