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Upregulation of Interleukin 21 and Interleukin 21 Receptor in Patients with Dermatomyositis and Polymyositis

摘要Background:The immunopathologic mechanism underlying dermatomyositis (DM) and polymyositis (PM) remains poorly understood.Many cytokines play a pathogenic role in DM and PM.lnterleukin 21 (IL-21) has a pleiotropic effect on inflammation regulation.This study aimed to detect the serum IL-21 level and investigate the expression of IL-21 and IL-21 receptor (IL-21 R) in muscle tissues of patients with DM and PM.Methods:Biopsied muscle samples were obtained from 11 patients with DM,12 with PM,and six controls;mRNA levels of IL-21 and IL-21 R were analyzed by real-time quantitative reverse transcription-polymerase chain reaction;and immunohistochemical staining was used to evaluate the protein expression of IL-21 and IL-21R.Serum samples were obtained from 36 patients with DM,19 with PM,and 20 healthy controls.The serum IL-21 level was detected by enzyme-linked immunosorbent assay.Results:The expression of IL-21 was upregulated in patients with DM and PM.The IL-21 mRNA level was significantly increased in muscle tissues of patients with DM and PM (DM vs.control,P =0.001;PM vs.control,P =0.001),whereas IL-21R mRNA level in patients with DM/PM was not statistically different from that of healthy controls.Immunohistochemical staining showed both I L-21 and IL-21R were significantly expressed in the inflammatory cells in muscle tissues of patients with DM and PM.The serum IL-21 level was also significantly higher in patients with DM/PM than in controls (DM vs.control,49.12 [45.28,60.07] pg/ml vs.42.54 [38.69,48.85] pg/ml,P =0.00l;PM vs.control,50.77 [44.19,60.62] pg/ml vs.42.54 [38.69,48.85] pg/ml,P =0.005).Conclusions:IL-21 expression is upregulated in patients with DM and PM in both muscle tissue and serum.In addition,IL-21R protein is highly expressed in affected muscle tissues of patients with DM and PM.IL-21 may play a pathogenic role through IL-21R in patients with DM and PM.

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作者单位 Research Institute of Neuromuscular and Neurodegenerative Diseases, Department of Neurology, Qilu Hospital, Shandong University, Jinan,Shandong 250012, China;Department of Neurology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, China [1] Research Institute of Neuromuscular and Neurodegenerative Diseases, Department of Neurology, Qilu Hospital, Shandong University, Jinan,Shandong 250012, China [2] Research Institute of Neuromuscular and Neurodegenerative Diseases, Department of Neurology, Qilu Hospital, Shandong University, Jinan,Shandong 250012, China;Brain Science Research Institute, Shandong University, Jinan, Shandong 250012, China [3]
栏目名称 Original Articles
DOI 10.4103/0366-6999.213419
发布时间 2017-09-27
基金项目
This study was supported by a grant from the National Nature Science Foundation of China
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中华医学杂志(英文版)

中华医学杂志(英文版)

2017年130卷17期

2101-2106页

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