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本文引用的文献

1
Sphingosine kinase 2 restricts T cell immunopathology but permits viral persistence.鞘氨醇激酶 2 限制 T 细胞免疫病理,但允许病毒持续存在。
J Clin Invest. 2020 Dec 1;130(12):6523-6538. doi: 10.1172/JCI125297.
2
Tcf1 cells are required to maintain the inflationary T cell pool upon MCMV infection.Tcf1 细胞在 MCMV 感染后维持扩张的 T 细胞库是必需的。
Nat Commun. 2020 May 8;11(1):2295. doi: 10.1038/s41467-020-16219-3.
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TIGIT limits immune pathology during viral infections.TIGIT 限制病毒感染期间的免疫病理。
Nat Commun. 2020 Mar 9;11(1):1288. doi: 10.1038/s41467-020-15025-1.
4
TCR Repertoire Characterization for T Cells Expanded in Response to hRSV Infection in Mice Immunized with a Recombinant BCG Vaccine.针对重组卡介苗疫苗免疫的小鼠感染 hRSV 后扩增的 T 细胞的 TCR 库特征分析。
Viruses. 2020 Feb 20;12(2):233. doi: 10.3390/v12020233.
5
Defining 'T cell exhaustion'.定义“T 细胞耗竭”。
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6
Viruses Teaching Immunology: Role of LCMV Model and Human Viral Infections in Immunological Discoveries.病毒教授免疫学:LCMV 模型和人类病毒感染在免疫学发现中的作用。
Viruses. 2019 Jan 27;11(2):106. doi: 10.3390/v11020106.
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Chronic hepatitis B virus infection.慢性乙型肝炎病毒感染。
Lancet. 2018 Nov 24;392(10161):2313-2324. doi: 10.1016/S0140-6736(18)31865-8.
8
Dynamics of Tissue-Specific CD8 T Cell Responses during West Nile Virus Infection.西尼罗河病毒感染期间组织特异性 CD8 T 细胞反应的动态变化。
J Virol. 2018 Apr 27;92(10). doi: 10.1128/JVI.00014-18. Print 2018 May 15.
9
T Cells in Nonlymphoid Tissues Give Rise to Lymph-Node-Resident Memory T Cells.非淋巴组织中的 T 细胞可产生淋巴结驻留记忆 T 细胞。
Immunity. 2018 Feb 20;48(2):327-338.e5. doi: 10.1016/j.immuni.2018.01.015.
10
CRISPR-mediated TCR replacement generates superior anticancer transgenic T cells.CRISPR 介导的 TCR 替换可产生更优的抗癌转基因 T 细胞。
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TCR转基因小鼠:研究病毒免疫发病机制的宝贵工具。

TCR Transgenic Mice: A Valuable Tool for Studying Viral Immunopathogenesis Mechanisms.

作者信息

Cho Yong-Bin, Lee In-Gu, Joo Yong-Hyun, Hong So-Hee, Seo Young-Jin

机构信息

Department of Life Science, Chung-Ang University, Seoul 06974, Korea.

Department of Biotechnology, The Catholic University of Korea, Bucheon 14662, Korea.

出版信息

Int J Mol Sci. 2020 Dec 18;21(24):9690. doi: 10.3390/ijms21249690.

DOI:10.3390/ijms21249690
PMID:33353154
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7765986/
Abstract

Viral infectious diseases are a significant burden on public health and the global economy, and new viral threats emerge continuously. Since CD4 and CD8 T cell responses are essential to eliminating viruses, it is important to understand the underlying mechanisms of anti-viral T cell-mediated immunopathogenesis during viral infections. Remarkable progress in transgenic (Tg) techniques has enabled scientists to more readily understand the mechanisms of viral pathogenesis. T cell receptor (TCR) Tg mice are extremely useful in studying T cell-mediated immune responses because the majority of T cells in these mice express specific TCRs for partner antigens. In this review, we discuss the important studies utilizing TCR Tg mice to unveil underlying mechanisms of T cell-mediated immunopathogenesis during viral infections.

摘要

病毒性传染病对公共卫生和全球经济造成了重大负担,并且新的病毒威胁不断出现。由于CD4和CD8 T细胞反应对于清除病毒至关重要,因此了解病毒感染期间抗病毒T细胞介导的免疫发病机制的潜在机制非常重要。转基因(Tg)技术的显著进展使科学家能够更容易地理解病毒发病机制。T细胞受体(TCR)Tg小鼠在研究T细胞介导的免疫反应中非常有用,因为这些小鼠中的大多数T细胞表达针对伴侣抗原的特异性TCR。在这篇综述中,我们讨论了利用TCR Tg小鼠揭示病毒感染期间T细胞介导的免疫发病机制潜在机制的重要研究。