The UniCAR system: A modular CAR T cell approach to improve the safety of CAR T cells

被引:77
|
作者
Bachmann, Michael [1 ,2 ,3 ,4 ,5 ]
机构
[1] HZDR, Inst Radiopharmaceut Canc Res, Dresden, Germany
[2] Carl Gustav Carus Tech Univ Dresden, Univ Canc Ctr UCC Dresden, Tumor Immunol, Dresden, Germany
[3] German Canc Consortium DKTK, Partner Site Dresden, Heidelberg, Germany
[4] German Canc Res Ctr, Heidelberg, Germany
[5] Natl Ctr Tumor Dis NCT, Partner Site Dresden, Dresden, Germany
基金
美国国家卫生研究院;
关键词
Immunotherapy; Chimeric antigen receptor; T cells; UniCAR; BiTE; Bispecific antibody; CHIMERIC ANTIGEN RECEPTOR; AUTOANTIGEN LA/SS-B; TUMOR-CELLS; CANCER; IMMUNOTHERAPY; LYMPHOCYTES; ANTIBODIES; CD19; SPECIFICITY; REDIRECTION;
D O I
10.1016/j.imlet.2019.05.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The idea to eliminate tumor cells via our own immune system is more than a hundred years old. However, a real break through came first with the development of check point inhibitors, bispecific antibodies (bsAbs) and T cells genetically modified to express Chimeric Antigen Receptors (CARs). Eventhough the clinical application of T cells equipped with CARS can lead to a complete remission, unfortunately, their application can also cause severe or even life threatening side effects as their activity can no more be adjusted once given to the patient. For targeting of tumor cells expressing tumor associated antigens (TAAs) which are not limited to tumor cells but also accessible on healthy tissues CAR T cells should not be permanently in a killing mode but be equipped with some kind of a switch whereby the activity of CAR T cells can reversely be turned "on and off ". Moreover, in case of cytokine release syndrome (CRS), tumor lysis syndrome (TLS), or other deadly side effects the possibility of an emergency shut down of the CAR T cell activity should exist. Modular CAR variants such as the UniCAR system may fulfill these requirements.
引用
收藏
页码:13 / 22
页数:10
相关论文
共 50 条
  • [41] A SNIPpet of safety: a Goldilocks approach in CAR-T therapy
    Benzaoui, Mehdi
    Taylor, Naomi
    Shah, Nirali N.
    [J]. CELL RESEARCH, 2022, 32 (07) : 603 - 604
  • [42] A SNIPpet of safety: a Goldilocks approach in CAR-T therapy
    Mehdi Benzaoui
    Naomi Taylor
    Nirali N. Shah
    [J]. Cell Research, 2022, 32 : 603 - 604
  • [43] A Theranostic Approach for CAR-T Cell Therapy
    Weber, Wolfgang A.
    Varasteh, Zohreh
    Fritschle, Katja
    Morath, Volker
    [J]. CLINICAL CANCER RESEARCH, 2022, 28 (24) : 5241 - 5243
  • [44] Sending CAR T Cells after T-cell Malignancies
    Poh, Alissa
    [J]. CANCER DISCOVERY, 2020, 10 (06) : 754 - 754
  • [45] Senolytic CAR T cells
    Hannah Stower
    [J]. Nature Medicine, 2020, 26 : 1009 - 1009
  • [46] CAR T Cells for Neuroblastoma
    Yeku, Oladapo O.
    Longo, Dan L.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2023, 388 (14): : 1328 - 1331
  • [47] CAR T cells in glioblastoma
    不详
    [J]. NATURE REVIEWS DRUG DISCOVERY, 2017, 16 (09)
  • [48] A Milestone for CAR T Cells
    Tran, Eric
    Longo, Dan L.
    Urba, Walter J.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2017, 377 (26): : 2593 - 2596
  • [49] Updates in CAR T cells
    June, Carl H.
    [J]. CYTOKINE, 2017, 100 : 22 - 22
  • [50] Updates on CAR T Cells
    June, Carl H.
    Scholler, John
    Ruella, Marco
    Fraietta, Joseph
    Melenhorst, J. Jos
    Ren, Jiangtao
    Zhao, Yangbing
    [J]. CANCER IMMUNOLOGY RESEARCH, 2018, 6 (09)