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Bone and cartilage destruction is one of the key manifestations of rheumatoid arthritis (RA). Although the role of T helper (Th)17 cells in these processes is clear, the role of IL-21-producing cells T cells has been neglected. We sought to investigate the role of IL-21 in RA by focusing on the functional characteristics of the main producers of this cytokine, synovial CD4+IL-21+ T cells. We show that the frequency of both synovial fluid (SF) CD4+IL-21+ or CD4+IL-21+TNF+ T cells in patients with RA was significantly higher compared with patients with psoriatic arthritis (PsA). The frequency of peripheral blood (PB) IL-21+CD4+ T cells in patients with RA positively correlated with disease activity score 28 (DAS28), serum anticyclic citrullinated peptide (anti-CCP) antibodies and IgM-rheumatoid factor (IgM-RF). IL-21 levels in RA SF were associated with matrix metalloproteinase (MMP)-1 and MMP-3. Related to this, IL-21 induced significantly the secretion of MMP-1 and MMP-3 in RA synovial biopsies. Sorted SF CD4+IL-21+ T cells significantly induced the release of MMP-1 and MMP-3 by fibroblast-like synoviocytes (FLS) compared with medium or CD4+IL-21- T cells in a coculture system. Neutralization of both IL-21 and TNF resulted in significantly less production of MMP by FLS. The results of this study indicate a new role for synovial CD4+IL-21+TNF+ T cells in promoting synovial inflammation/joint destruction in patients with RA. Importantly, IL-21 blockade in combination with anti-TNF might be an effective therapy in patients with RA by inhibiting MMP-induced inflammation/joint destruction.

Original publication

DOI

10.1189/jlb.5a0516-217rr

Type

Journal article

Journal

Journal of leukocyte biology

Publication Date

03/2017

Volume

101

Pages

775 - 783

Addresses

Department of Experimental Immunology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands; and.

Keywords

Joints, Synovial Fluid, CD4-Positive T-Lymphocytes, T-Lymphocytes, Helper-Inducer, Fibroblasts, Humans, Arthritis, Rheumatoid, Psoriasis, Peptides, Cyclic, Tumor Necrosis Factor-alpha, Immunoglobulin M, T-Box Domain Proteins, Interleukins, Interleukin-6, Interleukin-17, Rheumatoid Factor, Biopsy, Cell Proliferation, Proto-Oncogene Proteins c-bcl-6, Matrix Metalloproteinase 3, Matrix Metalloproteinase 1, RANK Ligand, Interferon-gamma, Synoviocytes