Interleukin-21 Receptor Might be a Novel Therapeutic Target for the Treatment of Rheumatoid Arthritis
Background Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by the synovial inflammation of the joints. Various cells and cytokines have been identified that may contribute to RA pathology. Interleukin (IL)-21 is a proinflammatory cytokine mediating pleiotropic functions throu...
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Published in | Journal of experimental & clinical medicine Vol. 6; no. 2; pp. 57 - 61 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.04.2014
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Subjects | |
Online Access | Get full text |
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Summary: | Background Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by the synovial inflammation of the joints. Various cells and cytokines have been identified that may contribute to RA pathology. Interleukin (IL)-21 is a proinflammatory cytokine mediating pleiotropic functions through the IL-21 receptor (IL-21R). Blockade of IL-21R may represent a hopeful therapeutic approach in RA. The aim of this study was to determine the percentage of IL-21R expressing CD4+ cells and IL-21 mRNA expression in peripheral blood of RA patients. Methods Surface expression of IL-21R on CD4+ cells in peripheral blood of RA patients ( n = 32 compared to healthy control participants ( n = 20) was evaluated by flow cytometry. Simultaneously, mononuclear cells were taken apart from the peripheral blood of individuals on a density gradient. The expression of IL-21 mRNA was assessed by real-time polymerase chain reaction. Results IL-21R-expressing CD4+ cells from RA patients showed a significantly higher percentage of IL-21R compared with healthy controls ( p < 0.05). Moreover, real-time polymerase chain reaction showed that there was no significant difference between patients and healthy controls. Conclusion Our results indicate higher expression of IL-21R in RA patients and suggest that targeting of the IL-21R may be a novel therapeutic idea for the treatment of RA. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 1878-3317 1878-3325 |
DOI: | 10.1016/j.jecm.2014.02.010 |