Programmable and multi-targeted CARs: a new breakthrough in cancer CAR-T cell therapy

被引:0
作者
S. Tahmasebi
R. Elahi
E. Khosh
A. Esmaeilzadeh
机构
[1] Tehran University of Medical Sciences,Department of Immunology, Health Faculty
[2] Zanjan University of Medical Sciences,School of Medicine
[3] Zanjan University of Medical Science,Department of Immunology
[4] Zanjan University of Medical Science,Cancer Gene Therapy Research Center
[5] Zanjan University of Medical Science,Immunotherapy Research and Technology Group
来源
Clinical and Translational Oncology | 2021年 / 23卷
关键词
Adoptive cell therapy; Conventional CARs; Multi-targeted CARs; Programmable CARs; Cancer; Immunotherapy;
D O I
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中图分类号
学科分类号
摘要
CAR-T cell therapy, as a novel immunotherapy approach, has indicated successful results in the treatment of hematological malignancies; however, distinct results have been achieved regarding solid tumors. Tumor immunosuppressive microenvironment has been identified as the most critical barrier in CAR-T cell therapy of solid tumors. Developing novel strategies to augment the safety and efficacy of CAR-T cells could be useful to overcome the solid tumor hurdles. Similar to other cancer treatments, CAR-T cell therapy can cause some side effects, which can disturb the healthy tissues. In the current review, we will discuss the practical breakthroughs in CAR-T cell therapy using the multi-targeted and programmable CARs instead of conventional types. These superior types of CAR-T cells have been developed to increase the function and safety of T cells in a controllable manner, which would diminish the incidence of relevant side effects. Moreover, we will describe the capability of these powerful CARs in targeting multiple tumor antigens, redirecting the CAR-T cells to specific target cells, incrementing the safety of CARs, and other advantages that lead to promising outcomes in cancer CAR-T cell therapy.
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页码:1003 / 1019
页数:16
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