首页|Progress,implications,and challenges in using humanized immune system mice in CAR-T therapy—Application evaluation and improvement

Progress,implications,and challenges in using humanized immune system mice in CAR-T therapy—Application evaluation and improvement

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In recent years,humanized immune system(HIS)mice have been gradually used as models for preclinical research in pharmacotherapies and cell therapies with major breakthroughs in tumor and other fields,better mimicking the human immune system and the tumor immune microenvironment,compared to traditional immunodeficient mice.To better promote the application of HIS mice in preclinical research,we se-lectively summarize the current prevalent and breakthrough research and evaluation of chimeric antigen receptor(CAR)-T cells in various antiviral and antitumor treat-ments.By exploring its application in preclinical research,we find that it can better reflect the actual clinical patient condition,with the advantages of providing high-efficiency detection indicators,even for progressive research and development.We believe that it has better clinical patient simulation and promotion for the updated design of CAR-T cell therapy than directly transplanted immunodeficient mice.The characteristics of the main models are proposed to improve the use defects of the existing models by reducing the limitation of antihost reaction,combining multiple models,and unifying sources and organoid substitution.Strategy study of relapse and toxicity after CAR-T treatment also provides more possibilities for application and development.

antitumorantiviralCAR-Thumanized immune system modelhumanized micepreclinical research

Hanwei Yue、Lin Bai

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NHC Key Laboratory of Human Disease Comparative Medicine,Institute of Laboratory Animal Sciences,CAMS and PUMC,Chao-yang District,Beijing,China

Chinese Academy of Medical Sciences(CAMS)Innovation Fund for Medical Sciences国家重点研发计划

2021-I2M-1-0352022YFA1103803

2024

动物模型与实验医学(英文)
中国实验动物学会,中国医学科学院医学实验动物研究所

动物模型与实验医学(英文)

ISSN:2096-5451
年,卷(期):2024.7(1)
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