T-cells "a la CAR-T(e)" - Genetically engineering T-cell response against cancer

被引:20
|
作者
Eisenberg, Vasyl [1 ]
Hoogi, Shiran [1 ]
Shamul, Astar [1 ]
Barliya, Tilda [1 ]
Cohen, Cyrille J. [1 ]
机构
[1] Bar Ilan Univ, Mina & Everard Goodman Fac Life Sci, Lab Tumor Immunol & Immunotherapy, IL-5290002 Ramat Gan, Israel
基金
以色列科学基金会;
关键词
CART cells; TCR gene transfer; Tumor Immunotherapy; CCR; NK receptors; Chimeric Receptors; CHIMERIC-ANTIGEN-RECEPTOR; CD19; CAR-T; PERIPHERAL-BLOOD LYMPHOCYTES; NATURAL-KILLER-CELLS; TUMOR-INFILTRATING LYMPHOCYTES; HUMAN RECOMBINANT ANTIBODIES; ENHANCED ANTITUMOR-ACTIVITY; TCR GENE-THERAPY; REPLICATION-COMPETENT RETROVIRUSES; COMPLEX-RESTRICTED SPECIFICITY;
D O I
10.1016/j.addr.2019.01.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The last decade will be remembered as the dawn of the immunotherapy era during which we have witnessed the approval by regulatory agencies of genetically engineered CAR T-cells and of checkpoint inhibitors for cancer treatment. Understandably, T-lymphocytes represent the essential player in these approaches. These cells can mediate impressive tumor regression in terminally-ill cancer patients. Moreover, they are amenable to genetic engineering to improve their function and specificity. In the present review, we will give an overview of the most recent developments in the field of T-cell genetic engineering including TCR-gene transfer and CAR T-cells strategies. We will also elaborate on the development of other types of genetic modifications to enhance their anti-tumor immune response such as the use of co-stimulatory chimeric receptors (CCRs) and unconventional CARs built on non-antibody molecules. Finally, we will discuss recent advances in genome editing and synthetic biology applied to T-cell engineering and comment on the next challenges ahead. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:23 / 40
页数:18
相关论文
共 50 条
  • [41] T-cell intrinsic Toll-like receptor signaling: implications for cancer immunotherapy and CAR T-cells
    Nouri, Yasmin
    Weinkove, Robert
    Perret, Rachel
    JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2021, 9 (11)
  • [42] REGULATION OF T-CELL RESPONSE TO P-AERUGINOSA POLYSACCHARIDE BY SUPPRESSOR T-CELLS ELICITED BY ANTIBACTERIAL T-CELLS
    MARKHAM, RB
    PIER, G
    POWDERLY, WG
    FASEB JOURNAL, 1988, 2 (04): : A885 - A885
  • [43] Combating challenges in CAR-T cells with engineering immunology
    Wang, Clement Yisai
    Cheung, Stephanie Po Ting
    Sugimura, Ryohichi
    FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2022, 10
  • [44] Engineering CAR-T cells with an integrated on/off switch
    Juillerat, A.
    Tkach, D.
    Busser, B.
    Temburni, S.
    Valton, J.
    Duclert, A.
    Poirot, L.
    Duchateau, P.
    HUMAN GENE THERAPY, 2018, 29 (12) : A120 - A121
  • [45] CAR-T cell therapy for T cell malignances
    Watanabe, Keisuke
    CANCER SCIENCE, 2025, 116 : 1784 - 1784
  • [46] CAR-T for the treatment of T cell malignancies
    DiPersio, John F.
    MEDICINE, 2019, 98 (26)
  • [47] CAR T Cells and T-Cell Therapies for Cancer: A Translational Science Review
    Brudno, Jennifer N.
    Maus, Marcela V.
    Hinrichs, Christian S.
    JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2024, 332 (22): : 1924 - 1935
  • [48] CAR-T cell therapy for T cell malignances
    Watanabe, Keisuke
    CANCER SCIENCE, 2024, 115 : 812 - 812
  • [49] CAR-T Cells for the Treatment of Lung Cancer
    Chocarro, Luisa
    Arasanz, Hugo
    Fernandez-Rubio, Leticia
    Blanco, Ester
    Echaide, Miriam
    Bocanegra, Ana
    Teijeira, Lucia
    Garnica, Maider
    Morilla, Idoia
    Martinez-Aguillo, Maite
    Pineiro-Hermida, Sergio
    Ramos, Pablo
    Lasarte, Juan Jose
    Vera, Ruth
    Kochan, Grazyna
    Escors, David
    LIFE-BASEL, 2022, 12 (04):
  • [50] Programming CAR-T cells to kill cancer
    Louai Labanieh
    Robbie G. Majzner
    Crystal L. Mackall
    Nature Biomedical Engineering, 2018, 2 : 377 - 391