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考古神经免疫学:从历史病例中复活的致病性免疫反应为人类自身免疫性脑脊髓炎和多发性硬化症提供了新的认识。

Archeological neuroimmunology: resurrection of a pathogenic immune response from a historical case sheds light on human autoimmune encephalomyelitis and multiple sclerosis.

机构信息

Institute of Clinical Neuroimmunology, University Hospital and Biomedical Center, Ludwig-Maximilians University Munich, Munich, Germany.

Department of Neuroimmunology, Center for Brain Research, Medical University of Vienna, Spitalgasse 4, 1090, Vienna, Austria.

出版信息

Acta Neuropathol. 2021 Jan;141(1):67-83. doi: 10.1007/s00401-020-02239-2. Epub 2020 Oct 29.

Abstract

Aim of our study was to identify the target auto-antigen in the central nervous system recognized by the immune system of a unique patient, who died more than 60 years ago from a disease with pathological changes closely resembling multiple sclerosis (MS), following a misguided immunization with lyophilized calf brain tissue. Total mRNA was isolated from formaldehyde fixed and paraffin embedded archival brain tissue containing chronic active inflammatory demyelinating lesions with inflammatory infiltrates rich in B-lymphocytes and plasma cells. Analysis of the transcriptome by next generation sequencing and reconstruction of the dominant antibody by bioinformatic tools revealed the presence of one strongly expanded B-cell clone, producing an autoantibody against a conformational epitope of myelin oligodendrocytes glycoprotein (MOG), similar to that recognized by the well characterized monoclonal anti-MOG antibody 8-18C5. The reconstructed antibody induced demyelination after systemic or intrathecal injection into animals with T-cell mediated encephalomyelitis. Our study suggests that immunization with bovine brain tissue in humans may-in a small subset of patients-induce a disease with an intermediate clinical and pathological presentation between MS and MOG-antibody associated inflammatory demyelinating disease (MOGAD).

摘要

我们的研究目的是确定一位独特患者的免疫系统在中枢神经系统中识别的自身抗原。该患者在 60 多年前因接受冻干小牛脑组织的免疫接种而导致疾病死亡,该疾病的病理变化与多发性硬化症(MS)非常相似。从福尔马林固定和石蜡包埋的存档脑组织中分离总 mRNA,该脑组织中含有慢性活动性炎症性脱髓鞘病变,炎症浸润富含 B 淋巴细胞和浆细胞。通过下一代测序对转录组进行分析,并通过生物信息学工具重建优势抗体,发现存在一个强烈扩增的 B 细胞克隆,产生针对髓鞘少突胶质细胞糖蛋白(MOG)构象表位的自身抗体,类似于特征明确的单克隆抗 MOG 抗体 8-18C5 所识别的表位。重建后的抗体在 T 细胞介导的脑炎动物中经系统或鞘内注射后可诱导脱髓鞘。我们的研究表明,人类用牛脑组织进行免疫接种可能会在一小部分患者中引发一种介于 MS 和 MOG 抗体相关性炎症性脱髓鞘疾病(MOGAD)之间的疾病,其临床表现和病理表现介于两者之间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fb8/7785560/8a810ec4d37f/401_2020_2239_Fig1_HTML.jpg

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