• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

MOG 抗体相关性脱髓鞘假瘤的脑组织病理研究与预后

Brain histopathological study and prognosis in MOG antibody-associated demyelinating pseudotumor.

机构信息

Department of Neurology The Third Affiliated Hospital of Sun Yat-Sen University Guangzhou 510630 China.

Department of Neurology the Second Affiliated Hospital of Guangzhou Medical University Guangzhou 510260 China.

出版信息

Ann Clin Transl Neurol. 2019 Jan 8;6(2):392-396. doi: 10.1002/acn3.712. eCollection 2019 Feb.

DOI:10.1002/acn3.712
PMID:30847372
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6389737/
Abstract

Our objective was to examine the brain biopsies by histopathology and investigate the prognosis of patients with myelin oligodendrocyte glycoprotein antibody-associated demyelinating pseudotumor. The clinical, MRI, and histological features of two patients with myelin oligodendrocyte glycoprotein antibody-associated demyelinating pseudotumor were reviewed. Both patients were treated with steroid plus rituximab and followed up. The brain biopsies of both cases revealed T cells, macrophages, and complement-mediated demyelination, which was in accord with multiple sclerosis-like pathology. Moreover, both cases showed favorable response to steroid plus rituximab therapy. Our cases add a new variant to the myelin oligodendrocyte glycoprotein-encephalomyelitis spectrum, which favorably responds to immunotherapy.

摘要

我们的目的是通过组织病理学检查脑活检,并研究髓鞘少突胶质细胞糖蛋白抗体相关脱髓鞘假瘤患者的预后。我们回顾了两名髓鞘少突胶质细胞糖蛋白抗体相关脱髓鞘假瘤患者的临床、MRI 和组织学特征。两名患者均接受类固醇加利妥昔单抗治疗并随访。这两个病例的脑活检均显示 T 细胞、巨噬细胞和补体介导的脱髓鞘,这与多发性硬化样病理学相符。此外,这两个病例对类固醇加利妥昔单抗治疗均有良好反应。我们的病例为髓鞘少突胶质细胞糖蛋白脑炎谱增加了一种新的变体,该变体对免疫疗法有良好的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f043/6389737/45571823700a/ACN3-6-392-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f043/6389737/d14917708773/ACN3-6-392-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f043/6389737/45571823700a/ACN3-6-392-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f043/6389737/d14917708773/ACN3-6-392-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f043/6389737/45571823700a/ACN3-6-392-g002.jpg

相似文献

1
Brain histopathological study and prognosis in MOG antibody-associated demyelinating pseudotumor.MOG 抗体相关性脱髓鞘假瘤的脑组织病理研究与预后
Ann Clin Transl Neurol. 2019 Jan 8;6(2):392-396. doi: 10.1002/acn3.712. eCollection 2019 Feb.
2
The myelin oligodendrocyte glycoprotein (MOG): a model for antibody-mediated demyelination in experimental autoimmune encephalomyelitis and multiple sclerosis.髓鞘少突胶质细胞糖蛋白(MOG):实验性自身免疫性脑脊髓炎和多发性硬化中抗体介导的脱髓鞘模型。
J Neural Transm Suppl. 2000(58):123-33. doi: 10.1007/978-3-7091-6284-2_10.
3
The N-terminal domain of the myelin oligodendrocyte glycoprotein (MOG) induces acute demyelinating experimental autoimmune encephalomyelitis in the Lewis rat.髓鞘少突胶质细胞糖蛋白(MOG)的N端结构域可在Lewis大鼠中诱发急性脱髓鞘性实验性自身免疫性脑脊髓炎。
J Neuroimmunol. 1995 Dec;63(1):17-27. doi: 10.1016/0165-5728(95)00124-7.
4
Influence of type I IFN signaling on anti-MOG antibody-mediated demyelination.I型干扰素信号传导对抗髓鞘少突胶质细胞糖蛋白抗体介导的脱髓鞘作用的影响。
J Neuroinflammation. 2017 Jun 24;14(1):127. doi: 10.1186/s12974-017-0899-1.
5
Antibody cross-linking of myelin oligodendrocyte glycoprotein leads to its rapid repartitioning into detergent-insoluble fractions, and altered protein phosphorylation and cell morphology.髓鞘少突胶质细胞糖蛋白的抗体交联导致其迅速重新分配到去污剂不溶性组分中,并改变蛋白质磷酸化和细胞形态。
J Neurosci. 2003 Jul 2;23(13):5461-71. doi: 10.1523/JNEUROSCI.23-13-05461.2003.
6
Immunopathogenic and clinical relevance of antibodies against myelin oligodendrocyte glycoprotein (MOG) in Multiple Sclerosis.多发性硬化症中抗髓鞘少突胶质细胞糖蛋白(MOG)抗体的免疫致病机制及临床相关性
J Neural Transm Suppl. 2000(60):351-60. doi: 10.1007/978-3-7091-6301-6_25.
7
Clinical and MRI phenotype of children with MOG antibodies.患有MOG抗体的儿童的临床和MRI表型
Mult Scler. 2016 Feb;22(2):174-84. doi: 10.1177/1352458515587751. Epub 2015 Jun 3.
8
Myelin oligodendrocyte glycoprotein and aquaporin-4 antibodies are highly specific in children with acquired demyelinating syndromes.髓鞘少突胶质细胞糖蛋白和水通道蛋白-4 抗体在获得性脱髓鞘综合征患儿中具有高度特异性。
Dev Med Child Neurol. 2018 Sep;60(9):958-962. doi: 10.1111/dmcn.13703. Epub 2018 Feb 22.
9
Signaling cascades activated upon antibody cross-linking of myelin oligodendrocyte glycoprotein: potential implications for multiple sclerosis.髓鞘少突胶质细胞糖蛋白抗体交联后激活的信号级联反应:对多发性硬化症的潜在影响。
J Biol Chem. 2005 Mar 11;280(10):8985-93. doi: 10.1074/jbc.M413174200. Epub 2005 Jan 4.
10
The role of myelin oligodendrocyte glycoprotein in autoimmune demyelination: a target for multiple sclerosis therapy?髓鞘少突胶质细胞糖蛋白在自身免疫性脱髓鞘中的作用:多发性硬化症治疗的靶点?
Expert Opin Ther Targets. 2012 May;16(5):451-62. doi: 10.1517/14728222.2012.677438. Epub 2012 Apr 12.

引用本文的文献

1
CNS B cell infiltration in tumefactive anti-myelin oligodendrocyte glycoprotein antibody-associated disease.肿胀性抗髓鞘少突胶质细胞糖蛋白抗体相关疾病中的中枢神经系统B细胞浸润
Mult Scler J Exp Transl Clin. 2024 Dec 5;10(4):20552173241301011. doi: 10.1177/20552173241301011. eCollection 2024 Oct-Dec.
2
Tumefactive demyelinating lesion and bilateral optic neuritis in a paediatric myelin oligodendrocyte glycoprotein antibody-associated disease.小儿髓鞘少突胶质细胞糖蛋白抗体相关疾病中的肿胀性脱髓鞘病变和双侧视神经炎
BMJ Case Rep. 2023 Dec 16;16(12):e255679. doi: 10.1136/bcr-2023-255679.
3
Pathogenesis, Clinical Features, and Treatment of Patients with Myelin Oligodendrocyte Glycoprotein (MOG) Autoantibody-Associated Disorders Focusing on Optic Neuritis with Consideration of Autoantibody-Binding Sites: A Review.

本文引用的文献

1
Different features between pediatric-onset and adult-onset patients who are seropositive for MOG-IgG: A multicenter study in South China.中国南方多中心研究:抗髓鞘少突胶质细胞糖蛋白抗体阳性的儿童与成人患者的不同特征。
J Neuroimmunol. 2018 Aug 15;321:83-91. doi: 10.1016/j.jneuroim.2018.05.014. Epub 2018 May 28.
2
Disease Course and Treatment Responses in Children With Relapsing Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease.儿童复发性髓鞘少突胶质细胞糖蛋白抗体相关疾病的病程和治疗反应。
JAMA Neurol. 2018 Apr 1;75(4):478-487. doi: 10.1001/jamaneurol.2017.4601.
3
MOG-antibody associated demyelinating disease of the CNS: A clinical and pathological study in Chinese Han patients.
髓鞘少突胶质细胞糖蛋白 (MOG) 自身抗体相关性疾病的发病机制、临床特征和治疗:关注视神经炎并考虑自身抗体结合位点的综述。
Int J Mol Sci. 2023 Aug 29;24(17):13368. doi: 10.3390/ijms241713368.
4
Pathology of myelin oligodendrocyte glycoprotein antibody-associated disease: a comparison with multiple sclerosis and aquaporin 4 antibody-positive neuromyelitis optica spectrum disorders.髓鞘少突胶质细胞糖蛋白抗体相关疾病的病理学:与多发性硬化症和水通道蛋白4抗体阳性视神经脊髓炎谱系障碍的比较。
Front Neurol. 2023 Jul 21;14:1209749. doi: 10.3389/fneur.2023.1209749. eCollection 2023.
5
Clinical spectrum and prognosis of pathologically confirmed atypical tumefactive demyelinating lesions.经病理证实的非典型肿块样脱髓鞘病变的临床谱及预后。
Sci Rep. 2023 May 13;13(1):7773. doi: 10.1038/s41598-023-34420-4.
6
Evolution in anti-myelin oligodendrocyte glycoprotein antibody detection and its clinical significance: a narrative review.抗髓鞘少突胶质细胞糖蛋白抗体检测的进展及其临床意义:一篇叙述性综述
Ann Transl Med. 2023 Apr 15;11(7):287. doi: 10.21037/atm-20-4547. Epub 2021 Jul 14.
7
The Potential Pathogenicity of Myelin Oligodendrocyte Glycoprotein Antibodies in the Optic Pathway.髓鞘少突胶质细胞糖蛋白抗体在视神经通路中的潜在致病性。
J Neuroophthalmol. 2023 Mar 1;43(1):5-16. doi: 10.1097/WNO.0000000000001772. Epub 2022 Dec 8.
8
Tumefactive Demyelination in MOG Ab-Associated Disease, Multiple Sclerosis, and AQP-4-IgG-Positive Neuromyelitis Optica Spectrum Disorder.MOG 抗体相关性疾病、多发性硬化症和 AQP-4-IgG 阳性视神经脊髓炎谱系疾病中的肿块样脱髓鞘病变。
Neurology. 2023 Mar 28;100(13):e1418-e1432. doi: 10.1212/WNL.0000000000206820. Epub 2023 Jan 23.
9
Central nervous system tumefactive demyelinating lesions: Risk factors of relapse and follow-up observations.中枢神经系统肿块样脱髓鞘病变:复发的危险因素及随访观察。
Front Immunol. 2022 Dec 1;13:1052678. doi: 10.3389/fimmu.2022.1052678. eCollection 2022.
10
Case report: MOG-IgG-associated encephalitis with Epstein-Barr virus infection and Alzheimer's pathologic change in cerebrospinal fluid.病例报告:伴有爱泼斯坦-巴尔病毒感染及脑脊液中阿尔茨海默病病理改变的MOG-IgG相关脑炎
Front Neurol. 2022 Dec 2;13:1013413. doi: 10.3389/fneur.2022.1013413. eCollection 2022.
MOG抗体相关的中枢神经系统脱髓鞘疾病:中国汉族患者的临床与病理研究
J Neuroimmunol. 2017 Apr 15;305:19-28. doi: 10.1016/j.jneuroim.2017.01.007. Epub 2017 Jan 12.
4
MOG-IgG in NMO and related disorders: a multicenter study of 50 patients. Part 2: Epidemiology, clinical presentation, radiological and laboratory features, treatment responses, and long-term outcome.视神经脊髓炎及相关疾病中的髓鞘少突胶质细胞糖蛋白免疫球蛋白G:50例患者的多中心研究。第2部分:流行病学、临床表现、影像学和实验室特征、治疗反应及长期预后
J Neuroinflammation. 2016 Sep 27;13(1):280. doi: 10.1186/s12974-016-0718-0.
5
MOG cell-based assay detects non-MS patients with inflammatory neurologic disease.MOG 细胞为基础的检测方法可用于诊断非 MS 炎性神经疾病患者。
Neurol Neuroimmunol Neuroinflamm. 2015 Mar 19;2(3):e89. doi: 10.1212/NXI.0000000000000089. eCollection 2015 Jun.
6
Histopathology and clinical course of MOG-antibody-associated encephalomyelitis.MOG 抗体相关性脑脊髓炎的组织病理学和临床病程。
Ann Clin Transl Neurol. 2015 Mar;2(3):295-301. doi: 10.1002/acn3.164. Epub 2015 Jan 14.
7
Pathologic heterogeneity persists in early active multiple sclerosis lesions.早期活动期多发性硬化病灶中存在病理异质性。
Ann Neurol. 2014 May;75(5):728-38. doi: 10.1002/ana.24163. Epub 2014 May 13.
8
Monofocal large inflammatory demyelinating lesion, mimicking brain glioma.单灶性大型炎性脱髓鞘病变,酷似脑胶质瘤。
Clin Neurol Neurosurg. 2009 Apr;111(3):296-9. doi: 10.1016/j.clineuro.2008.10.010. Epub 2008 Dec 5.
9
Heterogeneity of multiple sclerosis lesions: implications for the pathogenesis of demyelination.多发性硬化症病变的异质性:对脱髓鞘发病机制的影响。
Ann Neurol. 2000 Jun;47(6):707-17. doi: 10.1002/1531-8249(200006)47:6<707::aid-ana3>3.0.co;2-q.
10
Large focal tumor-like demyelinating lesions of the brain: intermediate entity between multiple sclerosis and acute disseminated encephalomyelitis? A study of 31 patients.大脑大型局灶性肿瘤样脱髓鞘病变:多发性硬化症与急性播散性脑脊髓炎之间的中间实体?31例患者的研究
Ann Neurol. 1993 Jan;33(1):18-27. doi: 10.1002/ana.410330105.