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通过细胞因子敲入基因替换提高人血液-淋巴系统小鼠。

Improving human hemato-lymphoid-system mice by cytokine knock-in gene replacement.

机构信息

Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06520, USA.

出版信息

Trends Immunol. 2011 Jul;32(7):321-7. doi: 10.1016/j.it.2011.04.005. Epub 2011 Jun 21.

Abstract

Human hemato-lymphoid-system mice hold great promise for modeling and studying important human diseases in vivo, and to enable vaccine testing. Until now, several major limitations have restricted the utility of human hemato-lymphoid-system mice in translational research. Recently, however, significant advances have been made in improving these mice, based on the delivery of human cytokines to create a better environment for human cells in the mouse host. In this review, we discuss the various approaches with a particular focus on improving human hemato-lymphoid-system mice by human cytokine knock-in gene replacement.

摘要

人源血液-淋巴系统小鼠在体内模拟和研究重要人类疾病,并进行疫苗测试方面具有巨大的潜力。但直到现在,一些主要的局限性限制了人源血液-淋巴系统小鼠在转化研究中的应用。然而,最近,通过向小鼠宿主中递送人细胞因子以创造更有利于人类细胞的环境,在改进这些小鼠方面取得了重大进展。在这篇综述中,我们讨论了各种方法,特别关注通过人细胞因子基因敲入替换来改进人源血液-淋巴系统小鼠。

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