Basal Eati, Gilligan Michael, Lesnick Connie, McKeon Andrew
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
Department of Neurology, University College Dublin, St Vincent's Hospital Elm Park, Dublin, Ireland.
Mov Disord. 2024 Dec;39(12):2271-2275. doi: 10.1002/mds.29991. Epub 2024 Aug 20.
There are more than 30 immunoglobulin G (IgG) autoantibody biomarkers of autoimmune cerebellar ataxia reported.
To describe a novel IgG biomarker targeting neurobeachin, a scaffolding protein integral to synapse formation and function.
Clinical and laboratory-based assessment was used for a novel diagnostic biomarker of autoimmune ataxia.
A 46-year-old woman had ataxia onset followed by bilateral knee pain, attributable to rheumatoid arthritis. She was negative for standard neural antibodies. Her ataxia stabilized and tremor initially improved after corticosteroid treatment, but she progressed to wheelchair-dependence (on methotrexate and then rituximab) over 4 years, in keeping with the trajectory encountered by many with autoimmune ataxia. In contrast, her inflammatory arthritis remitted with immunotherapy. Neurobeachin-IgG was unmasked in serum and cerebrospinal fluid using protein arrays and confirmed using neurobeachin-specific confocal immunofluorescence and Western blot.
Neurobeachin-IgG is a new neural antibody biomarker of cerebellar ataxia among a growing antibody repertoire, collectively common but often individually rare. © 2024 International Parkinson and Movement Disorder Society.
据报道,自身免疫性小脑共济失调有30多种免疫球蛋白G(IgG)自身抗体生物标志物。
描述一种针对神经beachin的新型IgG生物标志物,神经beachin是一种对突触形成和功能至关重要的支架蛋白。
采用基于临床和实验室的评估方法来寻找自身免疫性共济失调的新型诊断生物标志物。
一名46岁女性起病时出现共济失调,随后出现双侧膝关节疼痛,归因于类风湿关节炎。她的标准神经抗体检测呈阴性。皮质类固醇治疗后,她的共济失调得到稳定,震颤最初有所改善,但在4年时间里她逐渐发展到依赖轮椅(先后使用甲氨蝶呤和利妥昔单抗),这与许多自身免疫性共济失调患者的病程一致。相比之下,她的炎性关节炎通过免疫治疗得到缓解。利用蛋白质阵列在血清和脑脊液中检测到神经beachin-IgG,并通过神经beachin特异性共聚焦免疫荧光和蛋白质印迹法进行了确认。
在越来越多的抗体种类中,神经beachin-IgG是小脑共济失调的一种新的神经抗体生物标志物,这些抗体总体上常见但个体上往往罕见。© 2024国际帕金森病和运动障碍协会。