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本文引用的文献

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Minimal activation of memory CD8+ T cell by tissue-derived dendritic cells favors the stimulation of naive CD8+ T cells.组织来源的树突状细胞对记忆性CD8+ T细胞的激活作用微弱,这有利于对初始CD8+ T细胞的刺激。
Nat Immunol. 2007 Oct;8(10):1060-6. doi: 10.1038/ni1505. Epub 2007 Sep 2.
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Initial T cell receptor transgenic cell precursor frequency dictates critical aspects of the CD8(+) T cell response to infection.初始T细胞受体转基因细胞前体频率决定了CD8(+) T细胞对感染反应的关键方面。
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Acquisition of antigen presentasome (APS), an MHC/costimulatory complex, is a checkpoint of memory T-cell homeostasis.获得抗原呈递体(APS),一种主要组织相容性复合体/共刺激复合体,是记忆性T细胞稳态的一个检查点。
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4
Continuous recruitment of naive T cells contributes to heterogeneity of antiviral CD8 T cells during persistent infection.在持续性感染期间,幼稚T细胞的持续募集导致抗病毒CD8 T细胞的异质性。
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5
Intratumor CD4 T-cell accumulation requires stronger priming than for expansion and lymphokine secretion.肿瘤内CD4 T细胞的积累需要比其扩增和淋巴因子分泌更强的启动。
Cancer Res. 2006 May 15;66(10):5443-51. doi: 10.1158/0008-5472.CAN-05-3526.
6
CD4+ T cells that enter the draining lymph nodes after antigen injection participate in the primary response and become central-memory cells.抗原注射后进入引流淋巴结的CD4 + T细胞参与初次反应并成为中枢记忆细胞。
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7
Clonal competition inhibits the proliferation and differentiation of adoptively transferred TCR transgenic CD4 T cells in response to infection.克隆竞争抑制了过继转移的TCR转基因CD4 T细胞在感染应答中的增殖和分化。
J Immunol. 2006 Mar 1;176(5):3037-43. doi: 10.4049/jimmunol.176.5.3037.
8
CD4 T cells integrate signals delivered during successive DC encounters in vivo.CD4 T细胞整合体内连续与树突状细胞相遇期间传递的信号。
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9
Antigen-independent accumulation of activated effector/memory T lymphocytes into human and murine tumors.活化的效应/记忆T淋巴细胞在人和小鼠肿瘤中不依赖抗原的积累。
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10
The kinetic stability of MHC class II:peptide complexes is a key parameter that dictates immunodominance.MHC II类分子:肽复合物的动力学稳定性是决定免疫显性的关键参数。
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抗原特异性T细胞与T细胞相互作用调节CD4 T细胞扩增。

Antigen-specific T-T interactions regulate CD4 T-cell expansion.

作者信息

Helft Julie, Jacquet Alexandra, Joncker Nathalie T, Grandjean Isabelle, Dorothée Guillaume, Kissenpfennig Adrien, Malissen Bernard, Matzinger Polly, Lantz Olivier

机构信息

Laboratoire d'Immunologie Clinique, Inserm U653, Institut Curie, Paris.

出版信息

Blood. 2008 Aug 15;112(4):1249-58. doi: 10.1182/blood-2007-09-114389. Epub 2008 Jun 6.

DOI:10.1182/blood-2007-09-114389
PMID:18539897
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2515122/
Abstract

The regulation of CD4 T-cell numbers during an immune response should take account of the amount of antigen (Ag), the initial frequency of Ag-specific T cells, the mix of naive versus experienced cells, and (ideally) the diversity of the repertoire. Here we describe a novel mechanism of T-cell regulation that potentially deals with all of these parameters. We found that CD4 T cells establish a negative feedback loop by capturing their cognate major histocompatibility class (MHC)/peptide complexes from Ag-presenting cells and presenting them to Ag-experienced CD4 T cells, thereby inhibiting their recruitment into the response while allowing recruitment of naive T cells. The inhibition is Ag specific, begins at day 2 (long before Ag disappearance), and cannot be overcome by providing new Ag-loaded dendritic cells. In this way, CD4 T-cell proliferation is regulated in a functional relationship to the amount of Ag, while allowing naive T cells to generate repertoire variety.

摘要

免疫应答过程中CD4 T细胞数量的调节应考虑抗原(Ag)的量、Ag特异性T细胞的初始频率、幼稚细胞与记忆细胞的比例,以及(理想情况下)T细胞受体库的多样性。在此,我们描述了一种潜在涉及所有这些参数的T细胞调节新机制。我们发现,CD4 T细胞通过从抗原呈递细胞捕获其同源主要组织相容性复合体(MHC)/肽复合物,并将其呈递给已接触过Ag的CD4 T细胞,从而建立一个负反馈回路,进而抑制它们被招募进入应答反应,同时允许幼稚T细胞被招募。这种抑制是抗原特异性的,在第2天开始(远在抗原消失之前),并且不能通过提供新的负载抗原的树突状细胞来克服。通过这种方式,CD4 T细胞的增殖以与抗原量的功能关系进行调节,同时允许幼稚T细胞产生受体库多样性。