Microphysiological Systems for Cancer Immunotherapy Research and Development

被引:3
|
作者
Peng, Yansong [1 ]
Lee, Esak [1 ]
机构
[1] Cornell Univ, Nancy E & Peter C Meinig Sch Biomed Engn, Ithaca, NY 14853 USA
来源
ADVANCED BIOLOGY | 2024年 / 8卷 / 08期
关键词
engineered T cell therapy; immune checkpoint blockade; immunotherapy; microphysiological system; tumor immune microenvironment; CAR-T-CELLS; CHIP; MODELS; FIBROBLASTS; HALLMARKS; BLOCKADE; MICROENVIRONMENT; MICROFLUIDICS; REVEALS; FUTURE;
D O I
10.1002/adbi.202300077
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Cancer immunotherapy focuses on the use of patients' adaptive immune systems to combat cancer. In the past decade, FDA has approved many immunotherapy products for cancer patients who suffer from primary tumors, tumor relapse, and metastases. However, these immunotherapies still show resistance in many patients and often lead to inconsistent responses in patients due to variations in tumor genetic mutations and tumor immune microenvironment. Microfluidics-based organ-on-a-chip technologies or microphysiological systems have opened new ways that can provide relatively fast screening for personalized immunotherapy and help researchers and clinicians understand tumor-immune interactions in a patient-specific manner. They also have the potential to overcome the limitations of traditional drug screening and testing, given the models provide a more realistic 3D microenvironment with better controllability, reproducibility, and physiological relevance. This review focuses on the cutting-edge microphysiological organ-on-a-chip devices developed in recent years for studying cancer immunity and testing cancer immunotherapeutic agents, as well as some of the largest challenges of translating this technology to clinical applications in immunotherapy and personalized medicine.
引用
收藏
页数:15
相关论文
共 50 条
  • [1] Application of microphysiological systems in biopharmaceutical research and development
    Peterson, Norman C.
    Mahalingaiah, Prathap Kumar
    Fullerton, Aaron
    Di Piazza, Matteo
    [J]. LAB ON A CHIP, 2020, 20 (04) : 697 - 708
  • [2] Microphysiological systems for solid tumor immunotherapy: opportunities and challenges
    Abizanda-Campo, Sara
    Virumbrales-Munoz, Maria
    Humayun, Mouhita
    Marmol, Ines
    Beebe, David J.
    Ochoa, Ignacio
    Olivan, Sara
    Ayuso, Jose M.
    [J]. MICROSYSTEMS & NANOENGINEERING, 2023, 9 (01)
  • [3] Microphysiological systems for solid tumor immunotherapy: opportunities and challenges
    Sara Abizanda-Campo
    María Virumbrales-Muñoz
    Mouhita Humayun
    Ines Marmol
    David J. Beebe
    Ignacio Ochoa
    Sara Oliván
    Jose M. Ayuso
    [J]. Microsystems & Nanoengineering, 9
  • [4] Microphysiological systems for human aging research
    Park, Seungman
    Laskow, Thomas C.
    Chen, Jingchun
    Guha, Prasun
    Dawn, Buddhadeb
    Kim, Deok-Ho
    [J]. AGING CELL, 2024, 23 (03)
  • [5] Human microphysiological systems for drug development
    Roth, Adrian
    [J]. SCIENCE, 2021, 373 (6561) : 1304 - 1306
  • [6] Research and Development of Microphysiological Systems in Japan Supported by the AMED-MPS Project
    Ishida, Seiichi
    [J]. FRONTIERS IN TOXICOLOGY, 2021, 3
  • [7] The use of microphysiological systems to model metastatic cancer
    Jackson, Caitlin E.
    Green, Nicola H.
    English, William R.
    Claeyssens, Frederik
    [J]. BIOFABRICATION, 2024, 16 (03)
  • [8] Cancer immunology research toward development of personalized immunotherapy
    Kawakami, Yutaka
    [J]. CANCER SCIENCE, 2021, 112 : 241 - 241
  • [9] Microphysiological systems
    Hickman, James J.
    Huh, Dongeun
    Kamm, Roger D.
    [J]. APL BIOENGINEERING, 2019, 3 (04)
  • [10] Microphysiological Systems: Stakeholder Challenges to Adoption in Drug Development
    Hargrove-Grimes, Passley
    Low, Lucie A.
    Tagle, Danilo A.
    [J]. CELLS TISSUES ORGANS, 2022, 211 (03) : 269 - 281