• 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

血管周组织驻留记忆 T 细胞作为多发性硬化症的治疗靶点。

Perivascular tissue resident memory T cells as therapeutic target in multiple sclerosis.

机构信息

Neuroimmunology Research Group, Netherlands Institute for Neuroscience , Amsterdam, The Netherlands.

MS Center ErasMS, Departments of Neurology and Immunology, Erasmus Medical Center , Rotterdam, The Netherlands.

出版信息

Expert Rev Neurother. 2020 Aug;20(8):835-848. doi: 10.1080/14737175.2020.1776609. Epub 2020 Jun 30.

DOI:10.1080/14737175.2020.1776609
PMID:32476499
Abstract

INTRODUCTION

Multiple sclerosis (MS) is characterized by inflammatory attacks of infiltrating leukocytes at onset but evolves into a smoldering, progressive disease within the central nervous system at its later stages. The authors discuss the contribution of white matter lesions to the pathology of advanced MS, thereby paying particular attention to the role of T cells.

AREAS COVERED

Diagnostic biopsy and autopsy studies of white matter lesions in early MS show different pathological patterns of demyelination and leukocyte infiltration. Brain autopsies from advanced MS display substantial inflammation without distinct patterns and suggest a role for perivascular CD8 tissue-resident memory T (T) cells in active and mixed active/inactive MS white matter lesions. When compared to control and normal-appearing white matter, these lesions are enriched for parenchymal CD8 T cells. In the perivascular space, cuffs containing CD8 T cells are observed also in progressive MS, and could be sites of local reactivation.

EXPERT OPINION

Recent findings point toward the perivascular space as an immunological hotspot, which could be targeted in order to suppress a contribution of T cells to ongoing white matter lesion activity in advanced progressive MS. The authors discuss approaches, which may be explored to suppress T-cell reactivation in the perivascular space.

摘要

简介

多发性硬化症(MS)的特征是在发病时浸润白细胞的炎症攻击,但在后期阶段会演变为中枢神经系统的慢性、进行性疾病。作者讨论了脑白质病变对晚期 MS 病理学的贡献,特别关注 T 细胞的作用。

涵盖领域

早期 MS 脑白质病变的诊断性活检和尸检研究显示出不同的脱髓鞘和白细胞浸润病理模式。晚期 MS 的大脑尸检显示出大量的炎症,但没有明显的模式,并提示血管周围 CD8 组织驻留记忆 T(T)细胞在活跃和混合活跃/不活跃的 MS 脑白质病变中的作用。与对照和正常外观的白质相比,这些病变富含实质 CD8 T 细胞。在血管周围空间中,也可以在进行性 MS 中观察到含有 CD8 T 细胞的袖套,这可能是局部再激活的部位。

专家意见

最近的发现指向血管周围空间作为一个免疫热点,为了抑制 T 细胞对晚期进行性 MS 中持续的白质病变活动的贡献,可以针对该空间进行靶向治疗。作者讨论了可能探索的抑制血管周围空间 T 细胞再激活的方法。

相似文献

1
Perivascular tissue resident memory T cells as therapeutic target in multiple sclerosis.血管周组织驻留记忆 T 细胞作为多发性硬化症的治疗靶点。
Expert Rev Neurother. 2020 Aug;20(8):835-848. doi: 10.1080/14737175.2020.1776609. Epub 2020 Jun 30.
2
Tissue-resident memory T cells invade the brain parenchyma in multiple sclerosis white matter lesions.组织驻留记忆 T 细胞浸润多发性硬化症白质病变的脑组织。
Brain. 2020 Jun 1;143(6):1714-1730. doi: 10.1093/brain/awaa117.
3
Pathogenic Mechanisms Associated With Different Clinical Courses of Multiple Sclerosis.与多发性硬化症不同临床病程相关的发病机制。
Front Immunol. 2019 Jan 10;9:3116. doi: 10.3389/fimmu.2018.03116. eCollection 2018.
4
White matter lesions in multiple sclerosis are enriched for CD20 CD8 tissue-resident memory T cells.多发性硬化症中的白质病变富含 CD20+CD8+组织驻留记忆 T 细胞。
Eur J Immunol. 2021 Feb;51(2):483-486. doi: 10.1002/eji.202048665. Epub 2020 Oct 14.
5
Pathological differences between white and grey matter multiple sclerosis lesions.白质和灰质多发性硬化症病变之间的病理差异。
Ann N Y Acad Sci. 2015 Sep;1351:99-113. doi: 10.1111/nyas.12841. Epub 2015 Jul 22.
6
Clinical and pathological insights into the dynamic nature of the white matter multiple sclerosis plaque.对白质多发性硬化斑块动态性质的临床与病理见解。
Ann Neurol. 2015 Nov;78(5):710-21. doi: 10.1002/ana.24497. Epub 2015 Aug 24.
7
Phenotypic and functional characterization of T cells in white matter lesions of multiple sclerosis patients.多发性硬化症患者白质病变中T细胞的表型和功能特征
Acta Neuropathol. 2017 Sep;134(3):383-401. doi: 10.1007/s00401-017-1744-4. Epub 2017 Jun 17.
8
The compartmentalized inflammatory response in the multiple sclerosis brain is composed of tissue-resident CD8+ T lymphocytes and B cells.多发性硬化症大脑中的分隔性炎症反应由组织驻留的 CD8+ T 淋巴细胞和 B 细胞组成。
Brain. 2018 Jul 1;141(7):2066-2082. doi: 10.1093/brain/awy151.
9
Tissue-resident memory T cells in the multiple sclerosis brain and their relationship to Epstein-Barr virus infected B cells.多发性硬化症大脑中的组织驻留记忆T细胞及其与爱泼斯坦-巴尔病毒感染的B细胞的关系。
J Neuroimmunol. 2023 Mar 15;376:578036. doi: 10.1016/j.jneuroim.2023.578036. Epub 2023 Jan 26.
10
Dynamic Changes in Brain Mesenchymal Perivascular Cells Associate with Multiple Sclerosis Disease Duration, Active Inflammation, and Demyelination.脑间质周细胞的动态变化与多发性硬化症的病程、活跃性炎症和脱髓鞘有关。
Stem Cells Transl Med. 2017 Oct;6(10):1840-1851. doi: 10.1002/sctm.17-0028. Epub 2017 Sep 23.

引用本文的文献

1
Gemistocytic tumor cells programmed for glial scarring characterize T cell confinement in IDH-mutant astrocytoma.为胶质瘢痕形成编程的肥胖型肿瘤细胞是IDH突变型星形细胞瘤中T细胞受限的特征。
Nat Commun. 2025 Jan 29;16(1):1156. doi: 10.1038/s41467-025-56441-5.
2
NLRX1 limits inflammatory neurodegeneration in the anterior visual pathway.NLRX1限制前视觉通路中的炎性神经变性。
J Neuroinflammation. 2025 Jan 28;22(1):21. doi: 10.1186/s12974-025-03339-0.
3
Epstein-Barr virus, vitamin D and the immune response: connections with consequences for multiple sclerosis.
爱泼斯坦-巴尔病毒、维生素D与免疫反应:与多发性硬化症后果的关联
Front Immunol. 2024 Dec 23;15:1503808. doi: 10.3389/fimmu.2024.1503808. eCollection 2024.
4
Tissue-Resident Memory T Cells in Gastrointestinal Cancers: Prognostic Significance and Therapeutic Implications.胃肠道癌症中的组织驻留记忆T细胞:预后意义与治疗启示
Biomedicines. 2024 Jun 17;12(6):1342. doi: 10.3390/biomedicines12061342.
5
Osteopontin associates with brain T-cell transcriptome and compartmentalization in donors with and without multiple sclerosis.骨桥蛋白与患有和未患有多发性硬化症的供体的脑T细胞转录组及区室化相关。
iScience. 2022 Dec 9;26(1):105785. doi: 10.1016/j.isci.2022.105785. eCollection 2023 Jan 20.
6
Autoreactive lymphocytes in multiple sclerosis: Pathogenesis and treatment target.多发性硬化症中的自身反应性淋巴细胞:发病机制和治疗靶点。
Front Immunol. 2022 Sep 23;13:996469. doi: 10.3389/fimmu.2022.996469. eCollection 2022.
7
Single-cell profiling reveals periventricular CD56 NK cell accumulation in multiple sclerosis.单细胞分析揭示多发性硬化症中脑室周围CD56自然杀伤细胞的积聚。
Elife. 2022 May 10;11:e73849. doi: 10.7554/eLife.73849.
8
A systematic review of clinical and preclinical evidences for Janus kinase inhibitors in large vessel vasculitis.对Janus激酶抑制剂治疗大血管血管炎的临床和临床前证据的系统评价。
Clin Rheumatol. 2022 Jan;41(1):33-44. doi: 10.1007/s10067-021-05973-4. Epub 2021 Nov 3.
9
Cerebral Organoids-Challenges to Establish a Brain Prototype.类脑器官——建立大脑原型的挑战。
Cells. 2021 Jul 15;10(7):1790. doi: 10.3390/cells10071790.
10
CD8+ T Cell-Mediated Mechanisms Contribute to the Progression of Neurocognitive Impairment in Both Multiple Sclerosis and Alzheimer's Disease?CD8+ T 细胞介导的机制是否会导致多发性硬化症和阿尔茨海默病的神经认知障碍进展?
Front Immunol. 2020 Nov 19;11:566225. doi: 10.3389/fimmu.2020.566225. eCollection 2020.