Alisch Marlen, Foersterling Franziska, Zocholl Dario, Muinjonov Bakhrom, Schindler Patrick, Duchnow Ankelien, Otto Carolin, Ruprecht Klemens, Schmitz-Hübsch Tanja, Jarius Sven, Paul Friedemann, Siffrin Volker
Experimental and Clinical Research Center, Max-Delbrück-Center for Molecular Medicine and Charité-Universitätsmedizin Berlin, Berlin, Germany.
Institute for Biometry and Clinical Epidemiology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Glia. 2025 May;73(5):1090-1106. doi: 10.1002/glia.24675. Epub 2025 Jan 27.
Neuromyelitis optica spectrum disorders (NMOSD) are severe autoimmune conditions affecting the central nervous system. In a subset of cases, no autoantibodies are detectable with the currently used routine assays. This study aimed to determine whether the levels of expression of aquaporin-4 (AQP4), excitatory amino acid transporter 2 (EAAT2), or complement C3/C3d and C5b-9 in human astrocytes following incubation with patient sera under inflammatory conditions differ between the various NMOSD subtypes and whether such differences can help to identify autoantibody-mediated cases of NMOSD. Levels of AQP4, EAAT2, complement C3/C3d and C5b-9 epitope expression on human astrocytes pretreated with various cytokines were quantitatively analyzed via indirect immunofluorescence after exposure to sera from patients with AQP4-IgG seropositive, MOG-IgG seropositive, and AQP4/MOG-IgG double seronegative NMOSD. Significant differences in AQP4 and C3d epitope expression were observed, with IL-17A, IL-10, and IL-6 pre-treatment notably influencing astrocytic responses. Using uniform manifold approximation and projection (UMAP), patients were classified into clusters corresponding to AQP4-IgG seropositive, MOG-IgG seropositive, or double seronegative NMOSD. These results demonstrate distinct astrocytic staining patterns across NMOSD subtypes, providing a potential diagnostic tool for distinguishing between autoantibody-mediated astrocytopathy and other cases. These findings suggest specific pathogenic mechanisms linked to each NMOSD subtype, which may have implications for tailoring therapeutic strategies based on cytokine involvement and astrocyte reactivity.
视神经脊髓炎谱系障碍(NMOSD)是影响中枢神经系统的严重自身免疫性疾病。在一部分病例中,目前使用的常规检测方法无法检测到自身抗体。本研究旨在确定在炎症条件下,用患者血清孵育后人星形胶质细胞中水通道蛋白4(AQP4)、兴奋性氨基酸转运体2(EAAT2)或补体C3/C3d和C5b-9的表达水平在不同NMOSD亚型之间是否存在差异,以及这种差异是否有助于识别自身抗体介导的NMOSD病例。在用各种细胞因子预处理后的人星形胶质细胞上,通过间接免疫荧光定量分析AQP4、EAAT2、补体C3/C3d和C5b-9表位在暴露于AQP4-IgG血清阳性、MOG-IgG血清阳性和AQP4/MOG-IgG双血清阴性NMOSD患者血清后的表达水平。观察到AQP4和C3d表位表达存在显著差异,IL-17A、IL-10和IL-6预处理显著影响星形胶质细胞反应。使用均匀流形近似和投影(UMAP),将患者分为与AQP4-IgG血清阳性、MOG-IgG血清阳性或双血清阴性NMOSD相对应的簇。这些结果表明,不同NMOSD亚型的星形胶质细胞染色模式不同,为区分自身抗体介导的星形胶质细胞病和其他病例提供了一种潜在的诊断工具。这些发现提示了与每种NMOSD亚型相关的特定致病机制,这可能对基于细胞因子参与和星形胶质细胞反应性制定治疗策略具有启示意义。