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视神经脊髓炎谱系疾病中表达 EBI2 的 B 细胞与 AQP4-IgG:与急性发作和血清细胞因子的关联。

EBI2-expressing B cells in neuromyelitis optica spectrum disorder with AQP4-IgG: Association with acute attacks and serum cytokines.

机构信息

Department of Neurology, Korea University Anam Hospital, Korea University College of Medicine, Seoul, Republic of Korea.

Department of Neurology, Seoul National University Hospital, Seoul, Republic of Korea.

出版信息

J Neuroimmunol. 2021 Sep 15;358:577637. doi: 10.1016/j.jneuroim.2021.577637. Epub 2021 Jun 22.

Abstract

Epstein-Barr virus-induced G-protein coupled receptor 2 (EBI2) is important in regulating B cell activation. We investigated whether EBI2 expression on B cells is associated with acute attacks in neuromyelitis optica spectrum disorder with aquaporin-4 IgG (AQP4-IgG(+) NMOSD). Blood samples were collected from patients with AQP4-IgG(+) NMOSD, multiple sclerosis (MS), and patients without inflammatory demyelinating diseases (non-IDD controls). CD19+ B cells and CD4+ T cells were analyzed for surface expression of EBI2. Serum cytokine levels were also analyzed. The EBI2+CD19+ to EBI2-CD19+ cell ratio was significantly higher in patients with AQP4-IgG(+) NMOSD enrolled within 2 months of an attack than in those with non-IDDs (p = 0.007) and MS (p = 0.003). Patients with AQP4-IgG(+) NMOSD enrolled within 2 months of an attack had a higher EBI2+CD19+ cell frequency than patients with AQP4-IgG(+) NMOSD enrolled 2 months after a recent attack (p = 0.001). The EBI2+CD19+ cell frequency was positively correlated with interleukin (IL)-6 and IL-10. EBI2 expression on B cells could be associated with acute attacks of AQP4-IgG(+) NMOSD, possibly through IL-6- or IL-10-related pathways.

摘要

EB 病毒诱导的 G 蛋白偶联受体 2(EBI2)在调节 B 细胞激活中起重要作用。我们研究了 EBI2 在 B 细胞上的表达是否与水通道蛋白 4 免疫球蛋白 G(AQP4-IgG(+)NMOSD)相关的视神经脊髓炎谱系障碍的急性发作有关。从 AQP4-IgG(+)NMOSD、多发性硬化症(MS)和无炎症性脱髓鞘疾病(非 IDD 对照)患者中采集血液样本。分析 CD19+B 细胞和 CD4+T 细胞表面 EBI2 的表达。还分析了血清细胞因子水平。在急性发作后 2 个月内入组的 AQP4-IgG(+)NMOSD 患者中,EBI2+CD19+细胞与 EBI2-CD19+细胞的比例明显高于非 IDD 患者(p=0.007)和 MS 患者(p=0.003)。在急性发作后 2 个月内入组的 AQP4-IgG(+)NMOSD 患者的 EBI2+CD19+细胞频率高于最近一次急性发作后 2 个月入组的患者(p=0.001)。EBI2+CD19+细胞频率与白细胞介素(IL)-6 和 IL-10 呈正相关。B 细胞上的 EBI2 表达可能与 AQP4-IgG(+)NMOSD 的急性发作有关,可能通过 IL-6 或 IL-10 相关途径。

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