An immune system humanized mouse model targeting knockout of plk2 and a construction method and application thereof

By knocking out the PLK2 gene using the CRISPR/Cas9 system in human CD34+ hematopoietic stem cells, a humanized mouse model of the immune system with PLK2 knockout was constructed, solving the problem of low T lymphocyte reconstruction efficiency, achieving a significant increase in the proportion of human T cells, and providing a more efficient research tool.

CN122397685APending Publication Date: 2026-07-17INST OF LAB ANIMAL SCI CHINESE ACAD OF MEDICAL SCI

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
INST OF LAB ANIMAL SCI CHINESE ACAD OF MEDICAL SCI
Filing Date
2026-04-29
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

In existing humanized mouse models, T lymphocyte reconstitution efficiency is low and function is incomplete, which limits their application in T cell-dependent immunity research. Existing gene modification methods have limited effectiveness or lack specificity.

Method used

By knocking out the PLK2 gene in human CD34+ hematopoietic stem cells using the CRISPR/Cas9 gene editing system, a humanized mouse model of the immune system with targeted knockout of PLK2 was constructed, increasing the proportion of human CD3-positive T cells.

Benefits of technology

It significantly improved the reconstructed proportion of human T cells in humanized mouse models, provided a research tool that is closer to the composition and function of the human immune system, overcame the problem of low T cell reconstructed efficiency, and provided a more advantageous research platform.

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Abstract

本发明公开了一种靶向敲除PLK2的免疫系统人源化小鼠模型及其构建方法和应用,本发明属于生物医学技术领域,具体提供了一种利用CRISPR / Cas9基因编辑技术,在人CD34+造血干细胞中特异性敲除PLK2基因,并将该基因编辑细胞移植至免疫缺陷小鼠体内,最终获得人源化免疫系统的模型小鼠的方法。所构建的模型小鼠相较于传统人源化小鼠或敲除其他基因的对照模型,其体内重建的人源免疫细胞比例显著提升。该模型为研究人体免疫微环境、肿瘤免疫学及病原体感染与免疫应答提供了更优的研究工具,具有重要的应用价值。
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