Department of Anatomy and Cell Biology, University of Würzburg, Würzburg, Germany.
Institute of Anatomy and Cell Biology, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.
Acta Neuropathol. 2017 Aug;134(2):281-295. doi: 10.1007/s00401-017-1742-6. Epub 2017 Jun 15.
Multiple sclerosis (MS) is a chronic autoimmune disease of the central nervous system (CNS) in young adults that has serious negative socioeconomic effects. In addition to symptoms caused by CNS pathology, the majority of MS patients frequently exhibit gastrointestinal dysfunction, which was previously either explained by the presence of spinal cord lesions or not directly linked to the autoimmune etiology of the disease. Here, we studied the enteric nervous system (ENS) in a B cell- and antibody-dependent mouse model of MS by immunohistochemistry and electron microscopy at different stages of the disease. ENS degeneration was evident prior to the development of CNS lesions and the onset of neurological deficits in mice. The pathology was antibody mediated and caused a significant decrease in gastrointestinal motility, which was associated with ENS gliosis and neuronal loss. We identified autoantibodies against four potential target antigens derived from enteric glia and/or neurons by immunoprecipitation and mass spectrometry. Antibodies against three of the target antigens were also present in the plasma of MS patients as confirmed by ELISA. The analysis of human colon resectates provided evidence of gliosis and ENS degeneration in MS patients compared to non-MS controls. For the first time, this study establishes a pathomechanistic link between the well-established autoimmune attack on the CNS and ENS pathology in MS, which might provide a paradigm shift in our current understanding of the immunopathogenesis of the disease with broad diagnostic and therapeutic implications.
多发性硬化症(MS)是一种发生于年轻人中枢神经系统(CNS)的慢性自身免疫性疾病,对社会经济有严重的负面影响。除了由 CNS 病理引起的症状外,大多数 MS 患者还经常表现出胃肠道功能障碍,之前这一现象要么归因于脊髓病变的存在,要么与疾病的自身免疫病因没有直接关系。在这里,我们通过免疫组织化学和电子显微镜检查,在疾病的不同阶段研究了 B 细胞和抗体依赖性 MS 小鼠模型的肠神经系统(ENS)。ENS 退化在 CNS 病变和神经功能缺损的发生之前就已经很明显。该病理学是抗体介导的,导致胃肠道蠕动明显减少,这与 ENS 神经胶质增生和神经元丢失有关。我们通过免疫沉淀和质谱鉴定了来自肠神经胶质细胞和/或神经元的四个潜在靶抗原的自身抗体。通过 ELISA 证实,MS 患者的血浆中也存在针对三种靶抗原的抗体。对 MS 患者和非 MS 对照的结肠切除术标本的分析提供了证据,表明 MS 患者存在神经胶质增生和 ENS 退化。这项研究首次在中枢神经系统自身免疫攻击和 MS 中的 ENS 病理之间建立了一种发病机制联系,这可能会改变我们目前对疾病免疫发病机制的理解,具有广泛的诊断和治疗意义。