Ruland Tillmann, Wolbert Jolien, Gottschalk Michael G, König Simone, Schulte-Mecklenbeck Andreas, Minnerup Jens, Meuth Sven G, Groß Catharina C, Wiendl Heinz, Meyer Zu Hörste Gerd
Department of Neurology, University of Münster, Münster, Germany.
Department of Psychiatry and Psychotherapy, University of Münster, Münster, Germany.
Front Neurol. 2018 Jun 5;9:407. doi: 10.3389/fneur.2018.00407. eCollection 2018.
Primary angiitis of the central nervous system (PACNS) is a rare autoimmune vasculitis limited to the CNS often causing substantial disability. Understanding of this disease is impaired by the lack of available biomaterial. Here, we collected cerebrospinal fluid (CSF) from patients with PACNS and matched controls and performed unbiased proteomics profiling using ion mobility mass spectrometry to identify novel disease mechanisms and candidate biomarkers. We identified 14 candidate proteins, including amyloid-beta A4 protein (APP), with reduced abundance in the CSF of PACNS patients and validated APP by Enzyme-linked Immunosorbent Assay (ELISA) in an extended cohort of patients with PACNS. Subsequent functional annotation surprisingly suggested neuronal pathology rather than immune activation in PACNS. Our study is the first to employ mass spectrometry to local immune reactions in PACNS and it identifies candidates such as APP with pathogenic relevance in PACNS to improve patient care in the future.
中枢神经系统原发性血管炎(PACNS)是一种罕见的自身免疫性血管炎,仅限于中枢神经系统,常导致严重残疾。由于缺乏可用的生物材料,对这种疾病的了解受到了阻碍。在这里,我们收集了PACNS患者和匹配对照组的脑脊液(CSF),并使用离子淌度质谱进行了无偏蛋白质组学分析,以确定新的疾病机制和候选生物标志物。我们鉴定出14种候选蛋白,包括β-淀粉样蛋白A4(APP),其在PACNS患者脑脊液中的丰度降低,并通过酶联免疫吸附测定(ELISA)在更大的PACNS患者队列中验证了APP。随后的功能注释令人惊讶地表明,PACNS中存在神经元病理而非免疫激活。我们的研究首次采用质谱法研究PACNS中的局部免疫反应,并鉴定出诸如APP等在PACNS中具有致病相关性的候选物,以便未来改善患者护理。