多发性硬化
实验性自身免疫性脑脊髓炎
星形胶质细胞
视神经脊髓炎
神经科学
中枢神经系统
疾病
脱髓鞘病
免疫学
医学
小胶质细胞
表型
脑脊髓炎
自身免疫性疾病
神经免疫学
信号转导
神经系统
生物
自身免疫
药品
神经退行性变
临床试验
脱髓鞘病
水通道蛋白4
少突胶质细胞
细胞毒性
神经炎症
生物信息学
神经保护
封锁
治疗方法
神经学
格拉默
免疫系统
纳塔利祖玛
作者
Luhang Dai,Guo Cheng,Tingting Cui,Sitong He,Ran Wang,Jingqi Kang,Pei Li,Xin Zhang,Lei Zhang,Wei Zhang,Luting Yang,Yaling Zhang,Yaping Yan
出处
期刊:Cell Reports
[Cell Press]
日期:2026-02-01
卷期号:45 (2): 116913-116913
标识
DOI:10.1016/j.celrep.2025.116913
摘要
Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune inflammatory disease of the central nervous system (CNS) that, despite overlapping phenotypic features with multiple sclerosis (MS), manifests with more severe clinical outcomes. The defining pathogenic driver of NMOSD is the aquaporin-4 (AQP4) autoantibody, which induces astrocytic injury via complement-dependent cytotoxicity (CDC). MS is predominantly managed with disease-modifying therapies (DMTs) such as interferon-beta (IFN-β) to reduce relapse rates. However, these therapies are often ineffective or even detrimental in NMOSD. Our findings demonstrate that while IFN-β mitigates experimental autoimmune encephalomyelitis (EAE), it exacerbates NMOSD-like astrocytopathy. Deleting IFNAR1 counteracts this effect by selectively enhancing astrocyte activation without altering other CNS cells. Subsequently, we characterized multiple MS therapeutics that paradoxically worsen NMOSD-like pathology, whereas agents promoting astrocytic activation confer protection. Collectively, we establish a framework for astrocyte-centered drug screening and underscore the therapeutic potential of targeting astrocytes in NMOSD, connecting fundamental disease mechanisms to clinical applications.
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