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用于体内免疫反应追踪的TCR转基因T细胞的优化

Optimization of TCR transgenic T cells for in vivo tracking of immune responses.

作者信息

Stock Angus T, Mueller Scott N, Kleinert Lauren M, Heath William R, Carbone Francis R, Jones Claerwen M

机构信息

Department of Microbiology and Immunology, The University of Melbourne, Parkville, Victoria, Australia.

出版信息

Immunol Cell Biol. 2007 Jul;85(5):394-6. doi: 10.1038/sj.icb.7100076. Epub 2007 Jun 5.

DOI:10.1038/sj.icb.7100076
PMID:17549072
Abstract

T-cell receptor (TCR) transgenic mice have proven useful for the study of various immune parameters. Despite this, it has been suggested that transferred T cells respond differently to their endogenous counterparts at least in terms of conversion to antigen-experienced populations bearing memory cell markers. Here, we have compared the response of TCR transgenic T cells to endogenous populations within the context of infection with herpes simplex virus. We found that adoptive transfer at numbers approaching those of the endogenous virus-specific subset results in a response with similar kinetics, magnitude and memory subset conversion. This suggests that this form of optimized T-cell transfer remains a useful means of tracking antiviral immune responses.

摘要

T细胞受体(TCR)转基因小鼠已被证明对研究各种免疫参数很有用。尽管如此,有人认为,转移的T细胞与其内源性对应物的反应不同,至少在转化为带有记忆细胞标记的抗原经验丰富群体方面是如此。在这里,我们比较了TCR转基因T细胞与单纯疱疹病毒感染背景下内源性群体的反应。我们发现,以接近内源性病毒特异性亚群数量的方式进行过继转移会导致具有相似动力学、幅度和记忆亚群转化的反应。这表明这种优化的T细胞转移形式仍然是追踪抗病毒免疫反应的有用手段。

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Optimization of TCR transgenic T cells for in vivo tracking of immune responses.用于体内免疫反应追踪的TCR转基因T细胞的优化
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Characterization of two TCR transgenic mouse lines specific for herpes simplex virus.两种针对单纯疱疹病毒的TCR转基因小鼠品系的特性分析。
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Herpesvirus-Associated Lymphadenitis Distorts Fibroblastic Reticular Cell Microarchitecture and Attenuates CD8 T Cell Responses to Neurotropic Infection in Mice Lacking the STING-IFNα/β Defense Pathways.疱疹病毒相关性淋巴结炎会扭曲成纤维网状细胞的微结构,并削弱缺乏STING-IFNα/β防御途径的小鼠中CD8 T细胞对嗜神经性感染的反应。
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The transcription factor TFEB acts as a molecular switch that regulates exogenous antigen-presentation pathways.转录因子TFEB作为一种分子开关,调节外源性抗原呈递途径。
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Rapid proliferation and differentiation impairs the development of memory CD8+ T cells in early life.
快速增殖和分化会损害生命早期记忆性 CD8+T 细胞的发育。
J Immunol. 2014 Jul 1;193(1):177-84. doi: 10.4049/jimmunol.1400553. Epub 2014 May 21.
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CD4+ T cells modulate expansion and survival but not functional properties of effector and memory CD8+ T cells induced by malaria sporozoites.CD4+ T 细胞调节疟疾疟原虫诱导的效应和记忆 CD8+ T 细胞的扩增和存活,但不调节其功能特性。
PLoS One. 2011 Jan 4;6(1):e15948. doi: 10.1371/journal.pone.0015948.
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CD8(+) T lymphocyte mobilization to virus-infected tissue requires CD4(+) T-cell help.CD8(+) T 淋巴细胞向病毒感染组织的迁移需要 CD4(+) T 细胞的辅助。
Nature. 2009 Nov 26;462(7272):510-3. doi: 10.1038/nature08511. Epub 2009 Nov 8.
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Predicting CD62L expression during the CD8+ T-cell response in vivo.预测体内 CD8+T 细胞反应过程中 CD62L 的表达。
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Memory T cells in nonlymphoid tissue that provide enhanced local immunity during infection with herpes simplex virus.非淋巴组织中的记忆性T细胞,在单纯疱疹病毒感染期间提供增强的局部免疫力。
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Endogenous naive CD8+ T cell precursor frequency regulates primary and memory responses to infection.内源性初始CD8 + T细胞前体频率调节对感染的初次和记忆反应。
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