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Programmable and Multi-Targeted Cars: A New Breakthrough in Cancer Car-T Cell Therapy Publisher Pubmed



Tahmasebi S1 ; Elahi R2 ; Khosh E2 ; Esmaeilzadeh A3, 4, 5
Authors
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Authors Affiliations
  1. 1. Department of Immunology, Health Faculty, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran
  3. 3. Department of Immunology, Zanjan University of Medical Science, Zanjan, Iran
  4. 4. Cancer Gene Therapy Research Center, Zanjan University of Medical Science, Zanjan, Iran
  5. 5. Immunotherapy Research and Technology Group, Zanjan University of Medical Science, Zanjan, Iran

Source: Clinical and Translational Oncology Published:2021


Abstract

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. © 2020, Federacion de Sociedades Espanolas de Oncologia (FESEO).
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