Neurological Sciences and Cerebrovascular Research Laboratory, Department of Neurology, Neurology and Cerebrovascular Disease Group, Neuroscience Area La Paz Hospital Institute for Health Research-IdiPAZ (La Paz University Hospital-Universidad Autónoma de Madrid), Madrid, Spain.
Immunology Department, La Paz University Hospital, IdiPAZ Health Research Institute, Madrid, Spain.
Front Immunol. 2023 Aug 10;14:1224217. doi: 10.3389/fimmu.2023.1224217. eCollection 2023.
Multiple sclerosis is an inflammatory and demyelinating disease caused by a pathogenic immune response against the myelin sheath surfaces of oligodendrocytes. The demyelination has been classically associated with pathogenic B cells residing in the central nervous system that release autoreactive antibodies against myelin. The aim of the present study was to investigate whether extracellular vesicles (EVs) mediate delivery of myelin autoreactive antibodies from peripheral B cells against oligodendrocytes in multiple sclerosis (MS) and to analyze whether these EVs could mediate demyelination . We also studied the role of these EV-derived myelin antibodies as a diagnostic biomarker in MS.
This is a prospective, observational, and single-center study that includes patients with MS and two control groups: patients with non-immune white matter lesions and healthy controls. We isolated B-cell-derived EVs from the blood and cerebrospinal fluid (CSF) and analyzed their myelin antibody content. We also studied whether antibody-loaded EVs reach oligodendrocytes in patients with MS and the effect on demyelination of B-cell-derived EVs containing antibodies .
This study enrolled 136 MS patients, 23 white matter lesions controls, and 39 healthy controls. We found autoreactive myelin antibodies in EVs that were released by peripheral B cells, but not by populations of B cells resident in CSF. We also identified a cut-off of 3.95 ng/mL of myelin basic protein autoantibodies in EVs from peripheral B cells, with 95.2% sensitivity and 88.2% specificity, which allows us to differentiate MS patients from healthy controls. EV-derived myelin antibodies were also detected in the oligodendrocytes of MS patients. Myelin antibody-loaded EVs from B cells induced myelin markers decrease of oligodendrocytes .
Peripheral reactive immune cells could contribute remotely to MS pathogenesis by delivering myelin antibodies to oligodendrocytes. EV-derived myelin antibodies could play a role as diagnostic biomarker in MS.
多发性硬化症是一种由针对少突胶质细胞髓鞘表面的致病性免疫反应引起的炎症性和脱髓鞘性疾病。脱髓鞘与中枢神经系统中存在的致病性 B 细胞有关,这些 B 细胞释放针对髓鞘的自身反应性抗体。本研究旨在探讨细胞外囊泡 (EVs) 是否介导多发性硬化症 (MS) 患者外周 B 细胞释放的髓鞘自身反应性抗体对少突胶质细胞的传递,并分析这些 EV 是否可介导脱髓鞘。我们还研究了这些 EV 衍生的髓鞘抗体作为 MS 诊断生物标志物的作用。
这是一项前瞻性、观察性、单中心研究,纳入了 MS 患者和两个对照组:非免疫性脑白质病变患者和健康对照者。我们从血液和脑脊液 (CSF) 中分离出 B 细胞衍生的 EVs,并分析其髓鞘抗体含量。我们还研究了含有抗体的 B 细胞衍生 EV 是否能到达 MS 患者的少突胶质细胞以及对 EV 引起的脱髓鞘的影响。
这项研究纳入了 136 名 MS 患者、23 名脑白质病变对照者和 39 名健康对照者。我们发现,外周 B 细胞释放的 EV 中存在自身反应性髓鞘抗体,但 CSF 中常驻 B 细胞群中不存在。我们还确定了外周 B 细胞 EV 中髓鞘碱性蛋白自身抗体的截断值为 3.95ng/ml,其灵敏度为 95.2%,特异性为 88.2%,可将 MS 患者与健康对照者区分开来。MS 患者的少突胶质细胞中也检测到 EV 衍生的髓鞘抗体。B 细胞来源的负载髓鞘抗体的 EV 可诱导少突胶质细胞髓鞘标记物减少。
外周反应性免疫细胞可通过将髓鞘抗体输送到少突胶质细胞,从而在远处参与 MS 的发病机制。EV 衍生的髓鞘抗体可作为 MS 的诊断生物标志物。