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1
Identification of the genes specifically expressed in orally tolerized T cells.鉴定在口服耐受 T 细胞中特异性表达的基因。
Cytotechnology. 2003 Nov;43(1-3):73-80. doi: 10.1023/b:cyto.0000039918.80472.0e.
2
Orally tolerized T cells can form conjugates with APCs but are defective in immunological synapse formation.经口服耐受的T细胞可与抗原呈递细胞(APC)形成结合物,但在免疫突触形成方面存在缺陷。
J Immunol. 2005 Jul 15;175(2):829-38. doi: 10.4049/jimmunol.175.2.829.
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Comprehensive analysis of DNA methylation and gene expression in orally tolerized T cells.口服耐受 T 细胞中 DNA 甲基化和基因表达的综合分析。
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In vivo tolerization of Th1 lymphocytes following a single feeding with ovalbumin: anergy in the absence of suppression.用卵清蛋白单次喂食后Th1淋巴细胞的体内耐受:无抑制情况下的无反应性
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T-cell activation occurs simultaneously in local and peripheral lymphoid tissue following oral administration of a range of doses of immunogenic or tolerogenic antigen although tolerized T cells display a defect in cell division.口服一系列剂量的免疫原性或耐受性抗原后,T细胞活化在局部和外周淋巴组织中同时发生,尽管耐受的T细胞在细胞分裂方面存在缺陷。
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本文引用的文献

1
Th2 polarization enhanced by oral administration of higher doses of antigen.口服给予更高剂量抗原增强 Th2 极化。
Cytotechnology. 2000 Jul;33(1-3):237-45. doi: 10.1023/A:1008102304740.
2
Proteome analysis reveals caspase activation in hyporesponsive CD4 T lymphocytes induced in vivo by the oral administration of antigen.
J Biol Chem. 2003 Jul 25;278(30):27836-43. doi: 10.1074/jbc.M212820200. Epub 2003 May 7.
3
GRAIL: an E3 ubiquitin ligase that inhibits cytokine gene transcription is expressed in anergic CD4+ T cells.GRAIL:一种抑制细胞因子基因转录的E3泛素连接酶,在无反应性CD4 + T细胞中表达。
Immunity. 2003 Apr;18(4):535-47. doi: 10.1016/s1074-7613(03)00084-0.
4
T cell hyporesponsiveness induced by oral administration of ovalbumin is associated with impaired NFAT nuclear translocation and p27kip1 degradation.口服卵清蛋白诱导的T细胞低反应性与NFAT核转位受损及p27kip1降解有关。
J Immunol. 2002 Nov 1;169(9):4723-31. doi: 10.4049/jimmunol.169.9.4723.
5
Molecular cloning of a novel gene encoding a membrane-associated adaptor protein (LAX) in lymphocyte signaling.淋巴细胞信号传导中一种编码膜相关衔接蛋白(LAX)的新基因的分子克隆。
J Biol Chem. 2002 Nov 29;277(48):46151-8. doi: 10.1074/jbc.M208946200. Epub 2002 Sep 30.
6
Naive CD4+ T cells exhibit distinct expression patterns of cytokines and cell surface molecules on their primary responses to varying doses of antigen.初始CD4 + T细胞在对不同剂量抗原的初次反应中表现出细胞因子和细胞表面分子的不同表达模式。
J Immunol. 2002 Apr 1;168(7):3242-50. doi: 10.4049/jimmunol.168.7.3242.
7
The cell cycle dependent mislocalisation of emerin may contribute to the Emery-Dreifuss muscular dystrophy phenotype.埃默菌素的细胞周期依赖性定位错误可能导致埃默里-德赖富斯肌营养不良症的表型。
J Cell Sci. 2002 Jan 15;115(Pt 2):341-54. doi: 10.1242/jcs.115.2.341.
8
Distribution of soluble N-ethylmaleimide fusion protein attachment proteins (SNAPs) in the rat nervous system.
Neuroscience. 2001;107(3):363-71. doi: 10.1016/s0306-4522(01)00370-0.
9
Tob is a negative regulator of activation that is expressed in anergic and quiescent T cells.Tob是一种在无反应性和静止T细胞中表达的激活负调节因子。
Nat Immunol. 2001 Dec;2(12):1174-82. doi: 10.1038/ni730.
10
Interleukin-10-secreting Peyer's patch cells are responsible for active suppression in low-dose oral tolerance.分泌白细胞介素-10的派尔集合淋巴结细胞负责低剂量口服耐受中的主动抑制。
Immunology. 2001 Aug;103(4):458-64. doi: 10.1046/j.1365-2567.2001.01265.x.

鉴定在口服耐受 T 细胞中特异性表达的基因。

Identification of the genes specifically expressed in orally tolerized T cells.

机构信息

Department of Applied Biological Chemistry, The University of Tokyo, 1-1-1, Yayoj, Bunkyoku, Tokyo, 113-8657, Japan.

出版信息

Cytotechnology. 2003 Nov;43(1-3):73-80. doi: 10.1023/b:cyto.0000039918.80472.0e.

DOI:10.1023/b:cyto.0000039918.80472.0e
PMID:19003210
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3449604/
Abstract

Oral tolerance is the systemic immunological unresponsiveness that occurs after feeding protein antigens. Its physiological role is thought to be the prevention of hypersensitivity to food antigens, and its therapeutic use to treat inflammatory diseases has been suggested. Although it has been shown that CD4(+) T cells mediate oral tolerance, the precise molecular mechanisms remain unclear. In the present study, we employed suppression subtractive hybridization and identified 10 genes specifically expressed in orally tolerized T cells. These included genes that were interesting in terms of their putative functions in the negative regulation of T cell activation, e.g. Culin 1, LAX, and Zfhx1b, as well as four genes that encoded unknown proteins. We further investigated the expression of these genes in hyporesponsive T cells induced in vitro (in vitro anergized T cells). We found that six of the 10 genes were highly expressed in these cells, and kinetic studies suggested that one was associated with the induction of anergy, while the other five were associated with the maintenance of anergy. The remaining 4 genes that were not expressed in in vitro anergized T cells are also of interest as they may play a specific role in in vivo T cell tolerance. Functional analysis of these genes should help to understand the complex mechanisms underlying the induction and maintenance of oral tolerance, and moreover, in vivo immune tolerance in general.

摘要

口服耐受是在摄入蛋白抗原后发生的系统性免疫无应答。其生理作用被认为是预防对食物抗原的过敏反应,其治疗炎症性疾病的应用也已被提出。尽管已经表明 CD4(+) T 细胞介导了口服耐受,但确切的分子机制仍不清楚。在本研究中,我们采用抑制性消减杂交技术,鉴定了 10 个在口服耐受 T 细胞中特异性表达的基因。这些基因包括在 T 细胞激活的负调控方面具有潜在功能的基因,如 Culin 1、LAX 和 Zfhx1b,以及四个编码未知蛋白的基因。我们进一步研究了这些基因在体外诱导的低反应性 T 细胞(体外失能 T 细胞)中的表达。我们发现,这 10 个基因中有 6 个在这些细胞中高表达,动力学研究表明,其中一个与失能的诱导有关,而另外五个与失能的维持有关。另外 4 个在体外失能 T 细胞中不表达的基因也很有趣,因为它们可能在体内 T 细胞耐受中发挥特定作用。对这些基因的功能分析应该有助于理解诱导和维持口服耐受的复杂机制,进而有助于理解一般的体内免疫耐受。