The Long Noncoding RNA IFNG-AS1 Promotes T Helper Type 1 Cells Response in Patients with Hashimoto’s Thyroiditis

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作者
Huiyong Peng
Yingzhao Liu
Jie Tian
Jie Ma
Xinyi Tang
Ke Rui
Xinyu Tian
Chaoming Mao
Liwei Lu
Huaxi Xu
Pengcheng Jiang
Shengjun Wang
机构
[1] The Affiliated People’s Hospital,Department of Laboratory Medicine
[2] Jiangsu University,Department of Endocrinology
[3] Institute of Laboratory Medicine,Department of Pathology
[4] Jiangsu Key Laboratory of Laboratory Medicine,Department of General Surgery
[5] Jiangsu University School of Medicine,undefined
[6] The Affiliated People’s Hospital,undefined
[7] Jiangsu University,undefined
[8] The University of Hong Kong,undefined
[9] The Affiliated People’s Hospital,undefined
[10] Jiangsu University,undefined
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摘要
The long noncoding (lnc) RNA-Ifng-AS1 plays an essential role in the transcription of the gene encoding IFN-γ by Th1 cells and its human ortholog, IFNG-AS1, is expressed in human Th1 cells. However, IFNG-AS1 contributing to Th1 cells’ response in Hashimoto’s thyroiditis (HT) patients has not been reported. Twenty-eight HT patients and 20 healthy controls were enrolled in the study. The proportion of circulating Th1 cells and the level of T-bet, IFNG mRNA were increased in HT patients, the expression of IFNG-AS1 was upregulated and positively correlated with the proportion of circulating Th1 cells or T-bet and IFNG expression, or serum level of anti-thyroglobulin antibody/thyroperoxidase antibody in HT patients. IFNG-AS1 regulated the expression of IFNG at both transcriptional and translational level in human CD4+ T cells. Furthermore, strong positive correlations between the increased transcript level of IFNG-AS1 and the increased transcript level of T-bet or IFNG were revealed in thyroid tissues from HT patients. Our results indicate that enhanced expression of lncRNA-IFNG-AS1 contributes to Th1 cell response in HT patients and may be involved in the pathogenesis of HT.
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