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Car-Nk Cell: A New Paradigm in Tumor Immunotherapy Publisher



Marofi F1 ; Alawad AS2 ; Sulaiman Rahman H3, 4 ; Markov A5, 6 ; Abdelbasset WK7, 8 ; Ivanovna Enina Y9 ; Mahmoodi M10 ; Hassanzadeh A11 ; Yazdanifar M12 ; Stanley Chartrand M13 ; Jarahian M14
Authors
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Authors Affiliations
  1. 1. Immunology Research Center (IRC), Tabriz University of Medical Sciences, Tabriz, Iran
  2. 2. College of Medicine, University of Babylon, Babylon, Iraq
  3. 3. College of Medicine, University of Sulaimani, Sulaymaniyah, Iraq
  4. 4. Department of Medical Laboratory Sciences, Komar University of Science and Technology, Sulaymaniyah, Iraq
  5. 5. Tyumen State Medical University, Tyumen, Russian Federation
  6. 6. Tyumen Industrial University, Tyumen, Russian Federation
  7. 7. Department of Health and Rehabilitation Sciences, College of Applied Medical Sciences, Prince Sattam bin Abdulaziz University, Al Kharj, Saudi Arabia
  8. 8. Department of Physical Therapy, Kasr Al-Aini Hospital, Cairo University, Giza, Egypt
  9. 9. Sechenov First Moscow State Medical University, Moscow, Russian Federation
  10. 10. Department of Biology, School of Basic Science, Science and Research Branch, Islamic Azad University, Tehran, Iran
  11. 11. Department of Applied Cell Sciences, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran
  12. 12. Stem Cell Transplantation and Regenerative Medicine, Department of Pediatrics, Stanford University School of Medicine, Palo Alto, CA, United States
  13. 13. DigiCare Behavioral Research, Casa Grande, AZ, United States
  14. 14. German Cancer Research Center, Toxicology and Chemotherapy Unit (G401), Heidelberg, Germany

Source: Frontiers in Oncology Published:2021


Abstract

The tumor microenvironment (TME) is greatly multifaceted and immune escape is an imperative attribute of tumors fostering tumor progression and metastasis. Based on reports, the restricted achievement attained by T cell immunotherapy reflects the prominence of emerging other innovative immunotherapeutics, in particular, natural killer (NK) cells-based treatments. Human NK cells act as the foremost innate immune effector cells against tumors and are vastly heterogeneous in the TME. Currently, there exists a rapidly evolving interest in the progress of chimeric antigen receptor (CAR)-engineered NK cells for tumor immunotherapy. CAR-NK cells superiorities over CAR-T cells in terms of better safety (e.g., absence or minimal cytokine release syndrome (CRS) and graft-versus-host disease (GVHD), engaging various mechanisms for stimulating cytotoxic function, and high feasibility for ‘off-the-shelf’ manufacturing. These effector cells could be modified to target various antigens, improve proliferation and persistence in vivo, upturn infiltration into tumors, and defeat resistant TME, which in turn, result in a desired anti-tumor response. More importantly, CAR-NK cells represent antigen receptors against tumor-associated antigens (TAAs), thereby redirecting the effector NK cells and supporting tumor-related immunosurveillance. In the current review, we focus on recent progress in the therapeutic competence of CAR-NK cells in solid tumors and offer a concise summary of the present hurdles affecting therapeutic outcomes of CAR-NK cell-based tumor immunotherapies. © Copyright © 2021 Marofi, Al-Awad, Sulaiman Rahman, Markov, Abdelbasset, Ivanovna Enina, Mahmoodi, Hassanzadeh, Yazdanifar, Stanley Chartrand and Jarahian.
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