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鞘内免疫球蛋白 A 和 G 抗体针对边缘性脑炎患者的突触蛋白。

Intrathecal immunoglobulin A and G antibodies to synapsin in a patient with limbic encephalitis.

机构信息

Department of Neurology (J.P., K.R.) and Institute for Integrative Neuroanatomy (M.H., J.-F.Z., G.A.-H.), Charité-Universitätsmedizin Berlin; St. Josefs-Krankenhaus Potsdam (C.O., H.H.), Germany; the Department of Neuroscience and Brain Technologies (A.S., F.C., F.B.), Istituto Italiano di Tecnologia, Genova, Italy; the Department of Physiology and Cell Biology (D.G.), Faculty of Health Sciences and Zlotowski Center for Neuroscience, Ben-Gurion University of the Negev, Beer-Sheva, Israel; and the Institute of Toxicology (A.P.), Hannover Medical School, Germany.

出版信息

Neurol Neuroimmunol Neuroinflamm. 2015 Nov 4;2(6):e169. doi: 10.1212/NXI.0000000000000169. eCollection 2015 Dec.

Abstract

OBJECTIVE

To report on the identification of intrathecally synthesized immunoglobulin A (IgA) and immunoglobulin G (IgG) antibodies to synapsin, a synaptic vesicle-associated protein, in a patient with limbic encephalitis.

METHODS

Methods included clinical characterization, indirect immunofluorescence, immunoprecipitation, mass spectrometry, immunoblots of wild-type and synapsin I/II/III knockout mice, and cell-based assays with synapsin Ia, Ib, IIa, and IIb plasmids.

RESULTS

A 69-year-old man presented with confusion, disorientation, seizures, and left hippocampal hyperintensities on MRI. CSF examinations revealed an intrathecal IgA and IgG synthesis. Except for IgG antibodies to voltage-gated potassium channels in CSF, screening for known neuronal autoantibodies in serum and CSF was negative. However, indirect immunofluorescence using the patient's CSF showed binding of IgA to mouse hippocampus, amygdala, and cerebellum. Immunoprecipitation with CSF IgA followed by mass spectrometry identified synapsin as autoantigenic target. Knockout tissues and cell-based assays confirmed that IgA and IgG in the patient's CSF and serum reacted with synapsin Ia, Ib, and IIa. Calculation of antibody indices proved intrathecal synthesis of anti-synapsin IgA and IgG. The patient responded clinically to immunotherapy but developed left hippocampal atrophy. CSF IgA or IgG of the patient did not bind to live, unfixed, and nonpermeabilized mouse hippocampal neurons, compatible with synapsin being an intracellular antigen.

CONCLUSIONS

This report identifies isoforms of the synaptic vesicle-associated protein synapsin as targets of intrathecally produced IgA and IgG antibodies in a patient with limbic encephalitis. Future studies should clarify the prevalence and pathogenic relevance of anti-synapsin antibodies in limbic encephalitis.

摘要

目的

报告一例边缘性脑炎患者脑脊液中合成的免疫球蛋白 A(IgA)和免疫球蛋白 G(IgG)抗体识别突触相关蛋白突触素的情况。

方法

采用临床特征描述、间接免疫荧光、免疫沉淀、质谱分析、野生型和突触素 I/II/III 敲除小鼠免疫印迹以及突触素 Ia、Ib、IIa 和 IIb 质粒的细胞检测等方法。

结果

一名 69 岁男性以精神错乱、定向障碍、癫痫发作和左侧海马磁共振成像高信号为特征。CSF 检查显示存在鞘内 IgA 和 IgG 合成。除了 CSF 中电压门控钾通道 IgG 抗体外,血清和 CSF 中已知神经元自身抗体的筛查均为阴性。然而,患者 CSF 的间接免疫荧光显示 IgA 与小鼠海马、杏仁核和小脑结合。CSF IgA 免疫沉淀后进行质谱分析鉴定出突触素为自身抗原靶标。组织敲除和细胞检测证实患者 CSF 和血清中的 IgA 和 IgG 与突触素 Ia、Ib 和 IIa 反应。抗体指数的计算证明了抗突触素 IgA 和 IgG 的鞘内合成。患者对免疫治疗有临床反应,但出现左侧海马萎缩。患者 CSF 的 IgA 或 IgG 不能与活的、未经固定和非通透的小鼠海马神经元结合,这与突触素是细胞内抗原相符。

结论

本报告确定了突触相关蛋白突触素的同工型是边缘性脑炎患者鞘内产生的 IgA 和 IgG 抗体的靶标。未来的研究应阐明抗突触素抗体在边缘性脑炎中的流行率和致病相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30fd/4635552/ba8b8de8f8f9/NEURIMMINFL2015006312FF1.jpg

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