• 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

抗原致敏的CD4 T细胞在体内的克隆扩增能力降低,这是由免疫宿主中存在的因素所导致的。

Antigen-experienced CD4 T cells display a reduced capacity for clonal expansion in vivo that is imposed by factors present in the immune host.

作者信息

Merica R, Khoruts A, Pape K A, Reinhardt R L, Jenkins M K

机构信息

Department of Microbiology and Center for Immunology, University of Minnesota, Minneapolis, MN 55455, USA.

出版信息

J Immunol. 2000 May 1;164(9):4551-7. doi: 10.4049/jimmunol.164.9.4551.

DOI:10.4049/jimmunol.164.9.4551
PMID:10779756
Abstract

It is thought that protective immunity is mediated in part by Ag-experienced T cells that respond more quickly and vigorously than naive T cells. Using adoptive transfer of OVA-specific CD4 T cells from TCR transgenic mice as a model system, we show that Ag-experienced CD4 T cells accumulate in lymph nodes more rapidly than naive T cells after in vivo challenge with Ag. However, the magnitude of clonal expansion by Ag-experienced T cells was much less than that of naive T cells, particularly at early times after primary immunization. Ag-experienced CD4 T cells quickly reverted to the slower but more robust clonal expansion behavior of naive T cells after transfer into a naive environment. Conversely, the capacity for rapid clonal expansion was acquired by naive CD4 T cells after transfer into passively immunized recipients. These results indicate that rapid in vivo response by Ag-experienced T cells is facilitated by Ag-specific Abs, whereas the limited capacity for clonal expansion is imposed by some other factor in the immune environment, perhaps residual Ag.

摘要

据认为,保护性免疫部分是由经历过抗原的T细胞介导的,这些T细胞比初始T细胞反应更快、更强烈。我们使用来自TCR转基因小鼠的OVA特异性CD4 T细胞的过继转移作为模型系统,发现在体内用抗原攻击后,经历过抗原的CD4 T细胞比初始T细胞更快地在淋巴结中积累。然而,经历过抗原的T细胞的克隆扩增幅度远小于初始T细胞,特别是在初次免疫后的早期。经历过抗原的CD4 T细胞在转移到初始环境后,很快恢复到初始T细胞较慢但更稳健的克隆扩增行为。相反,初始CD4 T细胞在转移到被动免疫的受体后获得了快速克隆扩增的能力。这些结果表明,经历过抗原的T细胞在体内的快速反应由抗原特异性抗体促进,而克隆扩增能力的限制是由免疫环境中的其他因素造成的,可能是残留抗原。

相似文献

1
Antigen-experienced CD4 T cells display a reduced capacity for clonal expansion in vivo that is imposed by factors present in the immune host.抗原致敏的CD4 T细胞在体内的克隆扩增能力降低,这是由免疫宿主中存在的因素所导致的。
J Immunol. 2000 May 1;164(9):4551-7. doi: 10.4049/jimmunol.164.9.4551.
2
In vivo behavior of peptide-specific T cells during mucosal tolerance induction: antigen introduced through the mucosa of the conjunctiva elicits prolonged antigen-specific T cell priming followed by anergy.黏膜耐受诱导过程中肽特异性T细胞的体内行为:通过结膜黏膜引入的抗原引发抗原特异性T细胞的长期启动,随后出现无反应性。
J Immunol. 2000 May 1;164(9):4543-50. doi: 10.4049/jimmunol.164.9.4543.
3
Dynamics and requirements of T cell clonal expansion in vivo at the single-cell level: effector function is linked to proliferative capacity.体内单细胞水平T细胞克隆性扩增的动力学及需求:效应功能与增殖能力相关。
J Immunol. 1999 May 1;162(9):5212-23.
4
LFA-1 on CD4+ T cells is required for optimal antigen-dependent activation in vivo.CD4+ T细胞上的淋巴细胞功能相关抗原-1(LFA-1)是体内最佳抗原依赖性激活所必需的。
J Immunol. 2004 Oct 1;173(7):4443-51. doi: 10.4049/jimmunol.173.7.4443.
5
CD4 T cells monospecific to ovalbumin produced by Escherichia coli can induce colitis upon transfer to BALB/c and SCID mice.由大肠杆菌产生的对卵清蛋白单特异性的CD4 T细胞转移至BALB/c和SCID小鼠后可诱发结肠炎。
Int Immunol. 2001 Dec;13(12):1561-70. doi: 10.1093/intimm/13.12.1561.
6
Enteric infection acts as an adjuvant for the response to a model food antigen.肠道感染可作为对一种模型食物抗原反应的佐剂。
J Immunol. 2000 Dec 1;165(11):6174-82. doi: 10.4049/jimmunol.165.11.6174.
7
Indirect minor histocompatibility antigen presentation by allograft recipient cells in the draining lymph node leads to the activation and clonal expansion of CD4+ T cells that cause obliterative airways disease.引流淋巴结中同种异体移植受者细胞呈递间接次要组织相容性抗原,导致引起闭塞性气道疾病的CD4 + T细胞活化和克隆扩增。
J Immunol. 2004 Mar 15;172(6):3469-79. doi: 10.4049/jimmunol.172.6.3469.
8
In situ analysis reveals physical interactions between CD11b+ dendritic cells and antigen-specific CD4 T cells after subcutaneous injection of antigen.原位分析显示,皮下注射抗原后,CD11b+树突状细胞与抗原特异性CD4 T细胞之间存在物理相互作用。
J Immunol. 2002 Sep 1;169(5):2247-52. doi: 10.4049/jimmunol.169.5.2247.
9
NKT cell-dependent regulation of secondary antigen-specific, conventional CD4+ T cell immune responses.NKT 细胞依赖调节次级抗原特异性、常规 CD4+T 细胞免疫应答。
J Immunol. 2010 May 15;184(10):5589-94. doi: 10.4049/jimmunol.0903121. Epub 2010 Apr 7.
10
Cutting edge: in vivo identification of TCR redistribution and polarized IL-2 production by naive CD4 T cells.
J Immunol. 2001 Apr 1;166(7):4278-81. doi: 10.4049/jimmunol.166.7.4278.

引用本文的文献

1
The effect of abatacept on T-cell activation is not long-lived .阿巴西普对T细胞活化的作用并非持久。
Discov Immunol. 2024 Jan 4;3(1):kyad029. doi: 10.1093/discim/kyad029. eCollection 2024.
2
Follicular helper T cell profiles predict response to costimulation blockade in type 1 diabetes.滤泡辅助性T细胞谱可预测1型糖尿病对共刺激阻断的反应。
Nat Immunol. 2020 Oct;21(10):1244-1255. doi: 10.1038/s41590-020-0744-z. Epub 2020 Aug 3.
3
A Chlamydia trachomatis Strain Expressing Ovalbumin Stimulates an Antigen-Specific CD4 T Cell Response in Mice.
沙眼衣原体表达卵清蛋白的菌株在小鼠中刺激抗原特异性 CD4 T 细胞应答。
Infect Immun. 2019 Jun 20;87(7). doi: 10.1128/IAI.00837-18. Print 2019 Jul.
4
T cell-intrinsic IL-1R signaling licenses effector cytokine production by memory CD4 T cells.T 细胞内固有 IL-1R 信号通路许可记忆性 CD4 T 细胞产生效应细胞因子。
Nat Commun. 2018 Aug 9;9(1):3185. doi: 10.1038/s41467-018-05489-7.
5
Regulation of CD4 T cells and their effects on immunopathological inflammation following viral infection.CD4 T细胞的调控及其在病毒感染后对免疫病理炎症的影响。
Immunology. 2017 Oct;152(2):328-343. doi: 10.1111/imm.12771. Epub 2017 Jul 14.
6
Chronic Plasmodium chabaudi Infection Generates CD4 Memory T Cells with Increased T Cell Receptor Sensitivity but Poor Secondary Expansion and Increased Apoptosis.慢性查巴迪疟原虫感染产生具有更高T细胞受体敏感性但二次扩增能力差且凋亡增加的CD4记忆T细胞。
Infect Immun. 2017 Feb 23;85(3). doi: 10.1128/IAI.00744-16. Print 2017 Mar.
7
Transfer of in vivo primed transgenic T cells supports allergic lung inflammation and FIZZ1 and Ym1 production in an IL-4Rα and STAT6 dependent manner.体内致敏的转基因 T 细胞转移支持过敏肺炎症和 FIZZ1 和 Ym1 的产生,这依赖于 IL-4Rα 和 STAT6。
BMC Immunol. 2011 Oct 20;12:60. doi: 10.1186/1471-2172-12-60.
8
Modulating numbers and phenotype of CD8+ T cells in secondary immune responses.调节二次免疫应答中 CD8+T 细胞的数量和表型。
Eur J Immunol. 2010 Jul;40(7):1916-26. doi: 10.1002/eji.201040310.
9
Bioluminescence-based visualization of CD4 T cell dynamics using a T lineage-specific luciferase transgenic model.使用T细胞谱系特异性荧光素酶转基因模型基于生物发光对CD4 T细胞动力学进行可视化。
BMC Immunol. 2009 Aug 3;10:44. doi: 10.1186/1471-2172-10-44.
10
Macrophages: regulators of sex differences in asthma?巨噬细胞:哮喘性别差异的调节者?
Am J Respir Cell Mol Biol. 2010 May;42(5):595-603. doi: 10.1165/rcmb.2009-0016OC. Epub 2009 Jul 2.