免疫学
甲状腺
医学
FOXP3型
Treg细胞
遗传倾向
转录因子
免疫系统
疾病
格雷夫斯病
自身免疫
自身免疫性疾病
白细胞介素2受体
生物
T细胞
基因
遗传学
内分泌学
内科学
抗体
作者
Shiying Shao,Xuefeng Yu,Liya Shen
出处
期刊:Life Sciences
[Elsevier]
日期:2017-11-21
卷期号:192: 160-165
被引量:77
标识
DOI:10.1016/j.lfs.2017.11.026
摘要
Years of researches have demonstrated that the imbalance of Th17 and Tregs contribute to the thyroid autoimmunity and the severity of autoimmune thyroid disease (AITD). The underlying mechanism comprises inherent genetic predisposition, abnormality of Th17 and Treg related biological molecules, and gut microbiota disorder. New therapeutic strategies have been developed to improve the Th17/Treg equilibrium, including regulation of intracellular signaling pathways, neutralization of Th17-related cytokines, as well as manipulation of Th17 and Treg specific transcription factors. Although a few of these agents are applied into AITD, the clinic prospect is promising.
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