Elevated serum interleukin-27 levels in patients with systemic sclerosis: association with T cell, B cell and fibroblast activation
- Ayumi Yoshizaki1,
- Koichi Yanaba1,
- Yohei Iwata1,
- Kazuhiro Komura2,
- Asako Ogawa1,
- Eiji Muroi1,
- Fumihide Ogawa1,
- Motoi Takenaka1,
- Kazuhiro Shimizu1,
- Minoru Hasegawa2,
- Manabu Fujimoto2,
- Shinichi Sato1,3
- 1Department of Dermatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan
- 2Department of Dermatology, Kanazawa University Graduate School of Medical Science, Kanazawa, Japan
- 3Department of Dermatology, The University of Tokyo Graduate School of Medicine, Tokyo, Japan
- Correspondence to Dr Shinichi Sato, Department of Dermatology, The University of Tokyo Graduate School of Medicine, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan; satos-der{at}h.u-tokyo.ac.jp
- Accepted 10 July 2010
- Published Online First 12 August 2010
Abstract
Objective To determine serum levels of interleukin 27 (IL-27) in patients with systemic sclerosis (SSc) and relate the results to the clinical features of SSc.
Methods Serum levels of IL-27 in 91 patients with SSc and the production of IL-27 by isolated monocytes were examined by ELISA. The expression of IL-27 receptor in the skin fibroblasts, B cells and T cells was quantified by real-time PCR. The effect of IL-27 on immunoglobulin G (IgG) production of B cells, IL-17 production of CD4 T cells and proliferation and collagen synthesis of fibroblasts was also analysed.
Results Serum IL-27 levels were raised in patients with SSc compared with healthy controls and correlated positively with the extent of skin and pulmonary fibrosis and immunological abnormalities. IL-27 levels also correlated positively with serum levels of hyaluronan, recently identified as an endogenous ligand for Toll-like receptors. The retrospective longitudinal analysis showed a tendency for serum IL-27 levels to be attenuated during the follow-up period. IL-27 production by cultured monocytes was increased by hyaluronan stimulation. IL-27 receptor expression was upregulated in the affected skin fibroblasts, B cells and CD4 T cells of patients with SSc. Moreover, IL-27 stimulation increased IgG production of B cells, IL-17 production of CD4 T cells and proliferation and collagen synthesis of fibroblasts in patients with SSc compared with those in healthy controls.
Conclusion These results suggest that IL-27 and its signalling in B cells, T cells and fibroblasts contributes to disease development in patients with SSc.
Footnotes
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Funding This work was supported by a grant for Research on Intractable Diseases from the Ministry of Health, Labour and Welfare of Japan (to AY and SS).
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Competing interests None.
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Patient consent Obtained.
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Ethics approval This study was conducted with the approval of the Nagasaki University Hospital.
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Provenance and peer review Not commissioned; externally peer reviewed.
- Accepted 10 July 2010
- Published Online First 12 August 2010









