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

被引:0
|
作者
Hanwei Yue
Lin Bai
机构
[1] NHCKeyLaboratoryofHumanDiseaseComparativeMedicine,InstituteofLaboratoryAnimalSciences,CAMSandPUMC
关键词
D O I
暂无
中图分类号
R73-36 [治疗实验];
学科分类号
摘要
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 selectively summarize the current prevalent and breakthrough research and evaluation of chimeric antigen receptor(CAR)-T cells in various antiviral and antitumor treatments. 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.
引用
收藏
页码:3 / 11
页数:9
相关论文
共 29 条
  • [1] Progress, implications, and challenges in using humanized immune system mice in CAR-T therapy——Application evaluation and improvement
    Hanwei Yue
    Lin Bai
    Animal Models and Experimental Medicine, 2024, (01) : 3 - 11
  • [2] Progress, implications, and challenges in using humanized immune system mice in CAR-T therapy-Application evaluation and improvement
    Yue, Hanwei
    Bai, Lin
    ANIMAL MODELS AND EXPERIMENTAL MEDICINE, 2024, 7 (01) : 3 - 11
  • [3] Modelling CAR-T therapy in humanized mice
    Wu, Yongxia
    Yu, Xue-Zhong
    EBIOMEDICINE, 2019, 40 : 25 - 26
  • [4] CAR-T therapy for leukemia: progress and challenges
    Wang, Xin
    Xiao, Qing
    Wang, Zhe
    Feng, Wen-Li
    TRANSLATIONAL RESEARCH, 2017, 182 : 135 - 144
  • [5] CAR-T Therapy in GBM: Current Challenges and Avenues for Improvement
    Pant, Ayush
    Lim, Michael
    CANCERS, 2023, 15 (04)
  • [6] Humanized mice for immune system investigation: progress, promise and challenges
    Leonard D. Shultz
    Michael A. Brehm
    J. Victor Garcia-Martinez
    Dale L. Greiner
    Nature Reviews Immunology, 2012, 12 : 786 - 798
  • [7] Humanized mice for immune system investigation: progress, promise and challenges
    Shultz, Leonard D.
    Brehm, Michael A.
    Garcia-Martinez, J. Victor
    Greiner, Dale L.
    NATURE REVIEWS IMMUNOLOGY, 2012, 12 (11) : 786 - 798
  • [8] The application of CAR-T cell therapy in hematological malignancies: advantages and challenges
    Zhao, Zijun
    Chen, Yu
    Francisco, Ngiambudulu M.
    Zhang, Yuanqing
    Wu, Minhao
    ACTA PHARMACEUTICA SINICA B, 2018, 8 (04) : 539 - 551
  • [9] The application of CAR-T cell therapy in hematological malignancies: advantages and challenges
    Zijun Zhao
    Yu Chen
    Ngiambudulu M.Francisco
    Yuanqing Zhang
    Minhao Wu
    ActaPharmaceuticaSinicaB, 2018, 8 (04) : 539 - 551
  • [10] Improvement of CAR-T cell effectiveness using polyclonal Genome modifications and modulators of the innate immune system
    Perl, M.
    Knoedler, L.
    Becker, L. M.
    Shah, D.
    Schmidl, C.
    Poeck, H.
    ONCOLOGY RESEARCH AND TREATMENT, 2022, 45 (SUPPL 2) : 171 - 171