Jia Xi, Zhai Tianyu, Qu Chunjie, Ye Jianjun, Zhao Jing, Liu Xuerong, Zhang Jin-An, Qian Qiaohui
Department of Endocrinology, Shanghai University of Medicine and Health Sciences Affiliated Zhoupu Hospital, Shanghai, China.
Shanghai Pudong New Area Center for Disease Control, Shanghai, China.
Front Cell Dev Biol. 2021 May 28;9:685522. doi: 10.3389/fcell.2021.685522. eCollection 2021.
Hashimoto's thyroiditis (HT) is a common autoimmune disease characterized by high levels of thyroid peroxidase antibody (TPOAb) and thyroid globulin antibody (TgAb) as well as infiltration of lymphocytes in thyroid. In recent years, metformin has been proven to be effective in a variety of autoimmune diseases, such as systemic lupus erythematosus, rheumatoid arthritis and multiple sclerosis.
This study systematically explored the therapeutic effect of metformin on HT and its underlying mechanism by comprehensively utilizing methods including animal model, cell culture and differentiation, mRNA sequencing and 16S rRNA sequencing.
We found that metformin indeed had a therapeutic effect on mice with HT mainly by reducing TgAb and lymphocyte infiltration in thyroid tissue. In addition, metformin also significantly suppressed the number and function of Th17 cells and M1 macrophages polarization in HT mice. Furthermore, metformin can inhibit the differentiation and function of Th17 . The results of mRNA sequencing of thyroid tissue illustrated that the therapeutic effect of metformin on HT was mainly achieved by regulating immune pathways. 16S RNA sequencing of the intestinal flora found that the intestinal flora of HT mice differs significantly from that of the normal mice and also were altered by metformin treatment.
These experiments provided a preliminary theoretical basis for the clinical application of metformin in the treatment of HT.
桥本甲状腺炎(HT)是一种常见的自身免疫性疾病,其特征为甲状腺过氧化物酶抗体(TPOAb)和甲状腺球蛋白抗体(TgAb)水平升高以及甲状腺淋巴细胞浸润。近年来,二甲双胍已被证明对多种自身免疫性疾病有效,如系统性红斑狼疮、类风湿性关节炎和多发性硬化症。
本研究通过综合运用动物模型、细胞培养与分化、mRNA测序和16S rRNA测序等方法,系统地探讨了二甲双胍对HT的治疗效果及其潜在机制。
我们发现二甲双胍确实对HT小鼠具有治疗作用,主要是通过降低TgAb和甲状腺组织中的淋巴细胞浸润。此外,二甲双胍还显著抑制了HT小鼠中Th17细胞的数量和功能以及M1巨噬细胞极化。此外,二甲双胍可以抑制Th17的分化和功能。甲状腺组织的mRNA测序结果表明,二甲双胍对HT的治疗作用主要是通过调节免疫途径实现的。肠道菌群的16S RNA测序发现,HT小鼠的肠道菌群与正常小鼠有显著差异,并且也因二甲双胍治疗而发生改变。
这些实验为二甲双胍在HT治疗中的临床应用提供了初步的理论依据。