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本文引用的文献

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Targeted activation of human Vγ9Vδ2-T cells controls epstein-barr virus-induced B cell lymphoproliferative disease.靶向激活人 Vγ9Vδ2-T 细胞可控制 EBV 诱导的 B 细胞淋巴增殖性疾病。
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Adoptive transfer of EBV specific CD8+ T cell clones can transiently control EBV infection in humanized mice.EBV特异性CD8 + T细胞克隆的过继转移可暂时控制人源化小鼠中的EBV感染。
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Dengue virus infection induces broadly cross-reactive human IgM antibodies that recognize intact virions in humanized BLT-NSG mice.登革热病毒感染诱导广泛交叉反应的人 IgM 抗体,该抗体可识别人源化 BLT-NSG 小鼠中的完整病毒颗粒。
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Plasmacytoid dendritic cells suppress HIV-1 replication but contribute to HIV-1 induced immunopathogenesis in humanized mice.浆细胞样树突状细胞可抑制HIV-1复制,但在人源化小鼠中会促成HIV-1诱导的免疫病理发生。
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Modelling of human herpesvirus infections in humanized mice.人疱疹病毒感染的人源化小鼠模型。
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7
The use of BLT humanized mice to investigate the immune reconstitution of the gastrointestinal tract.使用 BLT 人源化小鼠研究胃肠道的免疫重建。
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Humanized mice as a model for aberrant responses in human T cell immunotherapy.人源化小鼠作为人类T细胞免疫治疗中异常反应的模型。
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9
Production of bone marrow, liver, thymus (BLT) humanized mice on the C57BL/6 Rag2(-/-)γc(-/-)CD47(-/-) background.在 C57BL/6 Rag2(-/-)γc(-/-)CD47(-/-)背景下生产骨髓、肝脏、胸腺(BLT)人源化小鼠。
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10
Insufficient interleukin-12 signalling favours differentiation of human CD4(+) and CD8(+) T cells into GATA-3(+) and GATA-3(+) T-bet(+) subsets in humanized mice.在人源化小鼠中,白细胞介素-12信号不足有利于人CD4(+)和CD8(+) T细胞分化为GATA-3(+)和GATA-3(+) T-bet(+)亚群。
Immunology. 2014 Oct;143(2):202-18. doi: 10.1111/imm.12304.

人源化小鼠在免疫学研究中的应用。

Application of Humanized Mice in Immunological Research.

作者信息

Tu Wenwei, Zheng Jian

机构信息

Department of Pediatrics & Adolescent Medicine, Li Ka Shing Faculty of Medicine, University of Hong Kong, Room L7-56, 7/F Laboratory Block, Faculty of Medicine Building, 21 Sassoon Road, Hong Kong, China.

出版信息

Methods Mol Biol. 2016;1371:157-76. doi: 10.1007/978-1-4939-3139-2_10.

DOI:10.1007/978-1-4939-3139-2_10
PMID:26530800
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7153430/
Abstract

During the past decade, the development of humanized mouse models and their general applications in biomedical research greatly accelerated the translation of outcomes obtained from basic research into potential diagnostic and therapeutic strategies in clinic. In this chapter, we firstly present an overview on the history and current progress of diverse humanized mouse models and then focus on those equipped with reconstituted human immune system. The update advancement in the establishment of humanized immune system mice and their applications in the studies of the development of human immune system and the pathogenesis of multiple human immune-related diseases are intensively reviewed here, while the shortcoming and perspective of these potent tools are discussed as well. As a valuable bridge across the gap between bench work and clinical trial, progressive humanized mouse models will undoubtedly continue to play an indispensable role in the wide area of biomedical research.

摘要

在过去十年中,人源化小鼠模型的发展及其在生物医学研究中的广泛应用极大地加速了从基础研究获得的成果向临床潜在诊断和治疗策略的转化。在本章中,我们首先概述各种人源化小鼠模型的历史和当前进展,然后重点介绍配备重建人免疫系统的模型。本文将深入综述人源化免疫系统小鼠建立方面的最新进展及其在人类免疫系统发育和多种人类免疫相关疾病发病机制研究中的应用,同时也将讨论这些强大工具的缺点和前景。作为跨越基础研究和临床试验之间差距的宝贵桥梁,不断进步的人源化小鼠模型无疑将继续在广泛的生物医学研究领域发挥不可或缺的作用。