NKG2D公司
白细胞介素21
免疫学
白细胞介素12
免疫系统
重症肌无力
生物
干扰素
细胞毒性T细胞
先天免疫系统
Janus激酶3
T细胞
体外
生物化学
作者
Ruiting Liu,Wěi Li,Dong Guo,Chunlin Yang,Jie Ding,Jianxin Xu,Rui‐Sheng Duan
标识
DOI:10.1016/j.intimp.2021.107880
摘要
Recent evidence has shown that natural killer (NK) cells have an immunoregulatory function in the pathogenesis of myasthenia gravis (MG). In this study, the phenotype and function of NK cell subsets in peripheral blood of new-onset MG (N-MG) and stable MG (S-MG) patients were explored. Circulating CD56dim and CD56bright NK cells were increased and decreased, respectively, in patients with N-MG and S-MG compared with healthy control (HC). Moreover, all circulating NK cell subsets from N-MG patients showed significantly lower expression of activating receptor NKG2D and production of Interferon (IFN) -γ than that from HC. The killing effects of NK cells on CD4+ T cells and Tfh cells were impaired in MG patients, whereas, they promoted the differentiation and activation of Tfh cells. These data indicated that the immune-regulation of NK cells on CD4+ T cells and Tfh cells in MG patients was abnormal, which may contribute to the immune-pathological mechanism of MG.
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