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DOI 10.1042/bsr20180096

Медицинская библиотека · Bioscience reports · 2018

Decreased expression of circulating Aire and increased Tfh/Tfr cells in myasthenia gravis patients.

Zhao Sijia, Ding Jiaqi, Wang Shengyuan, Li Chuan, Guo Peng, Zhang Min, Li Zhuyi

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Myasthenia gravis (MG) is a rare prototypical autoimmune disorder caused by antibodies (Ab) against postsynaptic membrane proteins. Most reports have investigated the role of autoimmune regulator gene (Aire) in thymic tissue in machianism of MG initiation. So far, the expression of Aire in human peripheral blood cells (we call it circulating Aire expression in the following passage) has not been reported. Herein, we explore the expression of Aire in peripharal blood, circulating T-follicular helper (cTfh) and T-follicular regulatory (cTfr) cells in MG patients. In our research, we found that the acetylcholine receptor (AChR) Ab level is higher in generalized MG (GMG) than that in ocular MG (OMG). Compared with the control group (CG), lower expression of Aire was found in MG patients, especially in GMG. The ratio of Tfh/Tfr was higher in GMG patients, and then in the OMG patients, and lowest in CG. All these differences above were statistically significant. Negative relation was discovered between expression of Aire in circulating blood and ratio of Tfh/Tfr, so did it exist between Aire expression and the severity of MG. Meanwhile, positive relation was discovered between ratio of Tfh/Tfr and the severity of MG. However, no significant relation was manifested in our study between the subset age of MG and Aire level. Overall, these findings imply circulating Aire might play a role in the imbalance of cTfh and cTfr cells and participate in the pathogenesis of MG.

Для цитирования: Zhao Sijia, Ding Jiaqi, Wang Shengyuan, Li Chuan, Guo Peng, Zhang Min, Li Zhuyi. Decreased expression of circulating Aire and increased Tfh/Tfr cells in myasthenia gravis patients.. Bioscience reports. 2018. DOI: 10.1042/bsr20180096.

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