Regulatory T cells but not T helper 17 cells are modulated in an animal model of Graves’ hyperthyroidism

被引:0
作者
Jin Zhou
Mei Bi
Chenling Fan
Xizhu Song
Rong Yang
Shujie Zhao
Li Li
Yushu Li
Weiping Teng
Zhongyan Shan
机构
[1] The First Hospital of China Medical University,The Endocrine Institute of China Medical University
[2] The First Hospital of China Medical University,The Liaoning Provincial Key Laboratory of Endocrine diseases
[3] The First Hospital of China Medical University,Department of Endocrinology and Metabolism
来源
Clinical and Experimental Medicine | 2012年 / 12卷
关键词
Th17; Treg; Graves’ hyperthyroidism; Th17/Treg ratio;
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摘要
Graves’ disease (GD) involves auto-immunity against thyroid cell antigens, but the reasons for the induction of auto-immunity are uncertain. We wished to investigate the role of T helper 17 (Th17) and regulatory T cells (Treg) in a mouse model of Graves’ hyperthyroidism. The model was generated by immunizing mice with adenovirus expressing the autoantigen thyroid-stimulating hormone receptor (Ad-TSHR289). The frequencies of splenic Th17 and Treg were determined by flow cytometry. The levels of interleukin-17(IL-17), forkhead box P3 (Foxp3), and orphan retinoic acid nuclear receptor (RORγt) mRNA were determined by real-time PCR. The number of CD4+CD25+Foxp3+ T lymphocyte was significantly reduced in the Ad-TSHR289 group compared with the Ad-control (P < 0.05). mRNA level for Foxp3 was less abundant in Ad-TSHR289 group compared with Ad-control (P < 0.05). However, CD4+IL-17+ T-cell subpopulation and expression of RORγt mRNA did not differ significantly between Ad-TSHR289 and Ad-control groups (P > 0.05). Nevertheless, in Ad-TSHR289 group, a profound increase in the Th17/Treg ratios was found. The present study demonstrates that Th17 is not involved in promoting Graves’ hyperthyroidism, while Treg and the ratio of Th17/Treg might play a role in the pathogenesis of Graves’ hyperthyroidism.
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页码:39 / 46
页数:7
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