• 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

使用髓鞘反应性CD4 + T细胞诱导被动性实验性自身免疫性脑脊髓炎

Induction of passive EAE using myelin-reactive CD4+ T cells.

作者信息

McPherson Rhoanne C, Cambrook Helen E, O'Connor Richard A, Anderton Stephen M

机构信息

MRC Centre for Inflammation Research and Centre for Multiple Sclerosis Research, Queen's Medical Research Institute, University of Edinburgh, 47 Little France Crescent, Edinburgh, EH16 4TJ, UK.

出版信息

Methods Mol Biol. 2014;1193:187-98. doi: 10.1007/978-1-4939-1212-4_17.

DOI:10.1007/978-1-4939-1212-4_17
PMID:25151007
Abstract

Experimental autoimmune encephalomyelitis (EAE) is an autoimmune disease of the central nervous system (CNS) often used as a model for the early inflammatory stages of multiple sclerosis and also as a model of organ-specific autoimmune disease.This protocol describes the induction of passive EAE in mice, either using T cells isolated from mice primed with myelin antigens, or through the use of naïve TCR transgenic T cells activated in vitro in the presence of myelin-derived antigens.

摘要

实验性自身免疫性脑脊髓炎(EAE)是一种中枢神经系统(CNS)的自身免疫性疾病,常被用作多发性硬化症早期炎症阶段的模型,也作为器官特异性自身免疫性疾病的模型。本方案描述了在小鼠中诱导被动性EAE的方法,既可以使用从用髓鞘抗原致敏的小鼠中分离的T细胞,也可以通过使用在髓鞘衍生抗原存在下体外激活的幼稚TCR转基因T细胞来实现。

相似文献

1
Induction of passive EAE using myelin-reactive CD4+ T cells.使用髓鞘反应性CD4 + T细胞诱导被动性实验性自身免疫性脑脊髓炎
Methods Mol Biol. 2014;1193:187-98. doi: 10.1007/978-1-4939-1212-4_17.
2
Host T cells are the main producers of IL-17 within the central nervous system during initiation of experimental autoimmune encephalomyelitis induced by adoptive transfer of Th1 cell lines.在通过Th1细胞系的过继转移诱导实验性自身免疫性脑脊髓炎起始阶段,宿主T细胞是中枢神经系统内白细胞介素-17的主要产生者。
J Immunol. 2008 Jun 15;180(12):8066-72. doi: 10.4049/jimmunol.180.12.8066.
3
Repertoire requirements of CD4+ T cells that prevent spontaneous autoimmune encephalomyelitis.预防自发性自身免疫性脑脊髓炎的CD4 + T细胞的 repertoire 要求。 (注:“repertoire”在这里可能有特定专业含义,比如免疫细胞的某种特性组合等,具体准确含义需结合专业背景进一步确定)
J Immunol. 2000 May 15;164(10):5499-507. doi: 10.4049/jimmunol.164.10.5499.
4
CD62L is required on effector cells for local interactions in the CNS to cause myelin damage in experimental allergic encephalomyelitis.在实验性变应性脑脊髓炎中,效应细胞上的CD62L对于中枢神经系统中的局部相互作用导致髓鞘损伤是必需的。
Immunity. 2001 Mar;14(3):291-302. doi: 10.1016/s1074-7613(01)00110-8.
5
Passive induction of experimental allergic encephalomyelitis.实验性变应性脑脊髓炎的被动诱导
Nat Protoc. 2006;1(4):1952-60. doi: 10.1038/nprot.2006.284.
6
Naive T lymphocytes traffic to inflamed central nervous system, but require antigen recognition for activation.初始T淋巴细胞迁移至炎症性中枢神经系统,但需要抗原识别才能被激活。
Eur J Immunol. 2000 Apr;30(4):1002-9. doi: 10.1002/(SICI)1521-4141(200004)30:4<1002::AID-IMMU1002>3.0.CO;2-2.
7
The influence of T cell Ig mucin-3 signaling on central nervous system autoimmune disease is determined by the effector function of the pathogenic T cells.T 细胞 Ig 黏液素-3 信号对中枢神经系统自身免疫性疾病的影响取决于致病性 T 细胞的效应功能。
J Immunol. 2013 May 15;190(10):4991-9. doi: 10.4049/jimmunol.1300083. Epub 2013 Apr 5.
8
Priming of myelin-specific T cells in the absence of dendritic cells results in accelerated development of Experimental Autoimmune Encephalomyelitis.在没有树突状细胞的情况下对髓鞘特异性 T 细胞进行激发会导致实验性自身免疫性脑脊髓炎的加速发展。
PLoS One. 2021 Apr 23;16(4):e0250340. doi: 10.1371/journal.pone.0250340. eCollection 2021.
9
Endogenous T Cell Receptor Rearrangement Represses Aggressive Central Nervous System Autoimmunity in a TcR-Transgenic Model on the Non-Obese Diabetic Background.内源性 T 细胞受体重排抑制非肥胖型糖尿病背景下 TcR 转基因模型中的中枢神经系统自身免疫的侵袭性。
Front Immunol. 2020 Jan 15;10:3115. doi: 10.3389/fimmu.2019.03115. eCollection 2019.
10
CD43 modulates severity and onset of experimental autoimmune encephalomyelitis.CD43调节实验性自身免疫性脑脊髓炎的严重程度和发病情况。
J Immunol. 2003 Dec 15;171(12):6527-33. doi: 10.4049/jimmunol.171.12.6527.

引用本文的文献

1
Trans-Endothelial Migration of Memory T Cells Is Impaired in Alemtuzumab-Treated Multiple Sclerosis Patients.在接受阿仑单抗治疗的多发性硬化症患者中,记忆T细胞的跨内皮迁移受损。
J Clin Med. 2022 Oct 24;11(21):6266. doi: 10.3390/jcm11216266.
2
Current Perspectives: Evidence to Date on BTK Inhibitors in the Management of Multiple Sclerosis.当前观点:BTK 抑制剂在多发性硬化症治疗中的现有证据。
Drug Des Devel Ther. 2022 Oct 6;16:3473-3490. doi: 10.2147/DDDT.S348129. eCollection 2022.
3
The role of the adaptive immune system and T cell dysfunction in neurodegenerative diseases.
适应性免疫系统和 T 细胞功能障碍在神经退行性疾病中的作用。
J Neuroinflammation. 2022 Oct 8;19(1):251. doi: 10.1186/s12974-022-02605-9.
4
The antimicrobial peptide cathelicidin drives development of experimental autoimmune encephalomyelitis in mice by affecting Th17 differentiation.抗菌肽 cathelicidin 通过影响 Th17 分化来驱动实验性自身免疫性脑脊髓炎在小鼠中的发展。
PLoS Biol. 2022 Aug 26;20(8):e3001554. doi: 10.1371/journal.pbio.3001554. eCollection 2022 Aug.
5
B Cells in Neuroinflammation: New Perspectives and Mechanistic Insights.神经炎症中的 B 细胞:新视角和机制见解。
Cells. 2021 Jun 26;10(7):1605. doi: 10.3390/cells10071605.
6
A LAT-Based Signaling Complex in the Immunological Synapse as Determined with Live Cell Imaging Is Less Stable in T Cells with Regulatory Capability.利用活细胞成像技术确定的免疫突触中基于 LAT 的信号复合物在具有调节能力的 T 细胞中不太稳定。
Cells. 2021 Feb 17;10(2):418. doi: 10.3390/cells10020418.
7
Tryptamine Attenuates Experimental Multiple Sclerosis Through Activation of Aryl Hydrocarbon Receptor.色胺通过激活芳烃受体减轻实验性多发性硬化症。
Front Pharmacol. 2021 Jan 25;11:619265. doi: 10.3389/fphar.2020.619265. eCollection 2020.
8
LPS-matured CD11c+ bone marrow-derived dendritic cells can initiate autoimmune pathology with minimal injection site inflammation.脂多糖成熟的CD11c⁺骨髓来源的树突状细胞能够在注射部位炎症极轻微的情况下引发自身免疫病理反应。
Lab Anim. 2017 Jun;51(3):292-300. doi: 10.1177/0023677216663584. Epub 2016 Aug 3.