• 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

T 细胞失能的分子机制。

Molecular mechanisms of T-cell anergy.

机构信息

Institute of Ecology and Genetics of Microorganisms, Ural Branch of the Russian Academy of Sciences, 614081 Perm, Russia.

出版信息

Biochemistry (Mosc). 2013 Feb;78(2):144-56. doi: 10.1134/S000629791302003X.

DOI:10.1134/S000629791302003X
PMID:23581985
Abstract

Anergy is a long-term stable state of T-lymphocyte unresponsiveness to antigenic stimulation associated with the blockade of IL-2 production and proliferation. Anergy is a pathway of peripheral tolerance formation. In this review, mechanisms underlying T-cell tolerization are considered in a classical in vitro model of clonal anergy, and these mechanisms are compared with different pathways of anergy induction in vivo. Special attention is given to regulatory T-lymphocytes because, on one hand, anergy is a specific feature of these cells, and on the other hand anergy is also a mechanism of their action on target cells - effector T-lymphocytes. The role of this phenomenon in the differentiation of regulatory T-cells and also in the development of activation-induced apoptosis in effector T-lymphocytes is discussed.

摘要

失能是 T 淋巴细胞对抗原刺激无反应的一种长期稳定状态,与白细胞介素 2 产生和增殖的阻断有关。失能是外周耐受形成的途径。在这篇综述中,我们考虑了克隆失能的经典体外模型中 T 细胞耐受形成的机制,并将这些机制与体内不同的失能诱导途径进行了比较。特别关注调节性 T 细胞,因为一方面,失能是这些细胞的一个特定特征,另一方面,失能也是它们对靶细胞 - 效应 T 细胞作用的一种机制。讨论了这种现象在调节性 T 细胞分化中的作用,以及在效应 T 细胞中激活诱导凋亡的发展中的作用。

相似文献

1
Molecular mechanisms of T-cell anergy.T 细胞失能的分子机制。
Biochemistry (Mosc). 2013 Feb;78(2):144-56. doi: 10.1134/S000629791302003X.
2
B7-blocking agents, alone or in combination with cyclosporin A, induce antigen-specific anergy of human memory T cells.B7阻断剂单独或与环孢素A联合使用,可诱导人记忆T细胞产生抗原特异性无反应性。
J Immunol. 1997 May 15;158(10):4734-40.
3
The role of ICOS in directing T cell responses: ICOS-dependent induction of T cell anergy by tolerogenic dendritic cells.诱导共刺激分子(ICOS)在指导T细胞应答中的作用:耐受性树突状细胞对T细胞无能的ICOS依赖性诱导。
J Immunol. 2009 Mar 15;182(6):3349-56. doi: 10.4049/jimmunol.0802733.
4
Dose-dependent induction of distinct anergic phenotypes: multiple levels of T cell anergy.不同无反应表型的剂量依赖性诱导:T细胞无反应的多个水平
J Immunol. 1999 Feb 15;162(4):1974-81.
5
Transcriptional basis of lymphocyte tolerance.淋巴细胞耐受性的转录基础。
Immunol Rev. 2006 Apr;210:105-19. doi: 10.1111/j.0105-2896.2006.00370.x.
6
Involvement of CTLA-4 in T-cell anergy induced by staphylococcal enterotoxin A in vitro.CTLA-4在体外葡萄球菌肠毒素A诱导的T细胞无能中的作用。
Mol Immunol. 2004 May;41(1):1-8. doi: 10.1016/j.molimm.2004.03.001.
7
Anergy of antigen-specific T lymphocytes is a potent mechanism of intravenously induced tolerance.抗原特异性T淋巴细胞失能是静脉注射诱导耐受的一种有效机制。
Immunology. 1994 Jun;82(2):294-300.
8
Antigen-experienced T cells undergo a transient phase of unresponsiveness following optimal stimulation.抗原致敏的T细胞在最佳刺激后会经历一个短暂的无反应期。
J Immunol. 1999 Dec 1;163(11):5929-36.
9
Coculture of Th cells with interleukin (IL)-7 in the absence of antigenic stimuli induced T-cell anergy reversed by IL-15.在无抗原刺激的情况下,将辅助性T细胞与白细胞介素(IL)-7 共培养会诱导T细胞无能,而IL-15可逆转这种无能状态。
Hum Immunol. 2005 Jun;66(6):677-87. doi: 10.1016/j.humimm.2005.02.006. Epub 2005 Mar 19.
10
Tolerogenic dendritic cells generated with different immunosuppressive cytokines induce antigen-specific anergy and regulatory properties in memory CD4+ T cells.不同免疫抑制细胞因子诱导生成的耐受树突状细胞在记忆性 CD4+T 细胞中诱导抗原特异性无反应性和调节特性。
J Immunol. 2010 Feb 15;184(4):1765-75. doi: 10.4049/jimmunol.0902133. Epub 2010 Jan 18.

引用本文的文献

1
A prospective clinical trial of GVHD prophylaxis with posttransplant cyclophosphamide and abatacept.一项关于移植后环磷酰胺和阿巴西普预防移植物抗宿主病的前瞻性临床试验。
Blood Adv. 2025 Aug 26;9(16):4336-4344. doi: 10.1182/bloodadvances.2024015094.
2
A Difficult Case of Calcineurin Inhibitor Neurotoxicity Post-Haploidentical HCT With a Successful Novel Solution: Cytotoxic T-Lymphocyte-Associated Protein 4-Immunoglobulin Blockade for GVHD Prophylaxis.钙调磷酸酶抑制剂同种异体造血干细胞移植后神经毒性的疑难病例:细胞毒性 T 淋巴细胞相关蛋白 4-免疫球蛋白阻断用于移植物抗宿主病预防的成功新方案。
Cell Transplant. 2024 Jan-Dec;33:9636897241265249. doi: 10.1177/09636897241265249.
3
Orai, STIM, and PMCA contribute to reduced calcium signal generation in CD8 T cells of elderly mice.
Orai、STIM 和 PMCA 导致老年小鼠 CD8 T 细胞中钙信号的产生减少。
Aging (Albany NY). 2020 Feb 12;12(4):3266-3286. doi: 10.18632/aging.102809.
4
Suboptimal stimulation by weak agonist epitope variants does not drive dysfunction of HIV-1-specific cytotoxic T lymphocyte clones.弱激动剂表位变异体的次优刺激不会导致 HIV-1 特异性细胞毒性 T 淋巴细胞克隆功能障碍。
AIDS. 2019 Aug 1;33(10):1565-1574. doi: 10.1097/QAD.0000000000002259.
5
T Cells and Regulated Cell Death: Kill or Be Killed.T 细胞与调控性细胞死亡:生死抉择。
Int Rev Cell Mol Biol. 2019;342:27-71. doi: 10.1016/bs.ircmb.2018.07.004. Epub 2018 Aug 29.
6
The Role of Natural Killer T Cells in Cancer-A Phenotypical and Functional Approach.自然杀伤 T 细胞在癌症中的作用——表型和功能方法。
Front Immunol. 2018 Feb 27;9:367. doi: 10.3389/fimmu.2018.00367. eCollection 2018.
7
Mechanisms of Tolerance Induction by Dendritic Cells .树突状细胞诱导耐受的机制。
Front Immunol. 2018 Feb 26;9:350. doi: 10.3389/fimmu.2018.00350. eCollection 2018.
8
MicroRNA-150 modulates intracellular Ca levels in naïve CD8 T cells by targeting TMEM20.MicroRNA-150 通过靶向 TMEM20 调节幼稚 CD8 T 细胞内的 Ca2+ 水平。
Sci Rep. 2017 Jun 1;7(1):2623. doi: 10.1038/s41598-017-02697-x.
9
Differential Cultivation of Induces Changes in the Immune Response to and Protective Efficacy of Whole Cell-Based Inactivated Vaccines.差异培养诱导对全细胞灭活疫苗的免疫反应和保护效力的变化。
Front Immunol. 2017 Jan 10;7:677. doi: 10.3389/fimmu.2016.00677. eCollection 2016.
10
Engineering immunity: Modulating dendritic cell subsets and lymph node response to direct immune-polarization and vaccine efficacy.工程化免疫:调节树突状细胞亚群及淋巴结反应以实现直接免疫极化和疫苗效力
J Control Release. 2015 Dec 10;219:610-621. doi: 10.1016/j.jconrel.2015.09.063. Epub 2015 Oct 20.