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CAR‐NK cell in cancer immunotherapy; A promising frontier

Chimeric antigen receptors (CARs) have a unique facet of synthetic biology and offer a paradigm shift in personalized medicine as they can use and redirect the patient's immune cells to attack cancer cells. CAR‐natural killer (NK) cells combine the targeted specificity of antigens with the subs...

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Autores principales: Marofi, Faroogh, Abdul‐Rasheed, Omar F., Rahman, Heshu Sulaiman, Budi, Hendrik Setia, Jalil, Abduladheem Turki, Yumashev, Alexei Valerievich, Hassanzadeh, Ali, Yazdanifar, Mahboubeh, Motavalli, Roza, Chartrand, Max Stanley, Ahmadi, Majid, Cid‐Arreguid, Angel, Jarahian, Mostafa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8409419/
https://www.ncbi.nlm.nih.gov/pubmed/34050690
http://dx.doi.org/10.1111/cas.14993
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author Marofi, Faroogh
Abdul‐Rasheed, Omar F.
Rahman, Heshu Sulaiman
Budi, Hendrik Setia
Jalil, Abduladheem Turki
Yumashev, Alexei Valerievich
Hassanzadeh, Ali
Yazdanifar, Mahboubeh
Motavalli, Roza
Chartrand, Max Stanley
Ahmadi, Majid
Cid‐Arreguid, Angel
Jarahian, Mostafa
author_facet Marofi, Faroogh
Abdul‐Rasheed, Omar F.
Rahman, Heshu Sulaiman
Budi, Hendrik Setia
Jalil, Abduladheem Turki
Yumashev, Alexei Valerievich
Hassanzadeh, Ali
Yazdanifar, Mahboubeh
Motavalli, Roza
Chartrand, Max Stanley
Ahmadi, Majid
Cid‐Arreguid, Angel
Jarahian, Mostafa
author_sort Marofi, Faroogh
collection PubMed
description Chimeric antigen receptors (CARs) have a unique facet of synthetic biology and offer a paradigm shift in personalized medicine as they can use and redirect the patient's immune cells to attack cancer cells. CAR‐natural killer (NK) cells combine the targeted specificity of antigens with the subsequent intracellular signaling ability of the receptors to increase their anti‐cancer functions. Importantly, CAR‐NK cells can be utilized as universal cell‐based therapy without requiring human leukocyte antigen (HLA) matching or earlier contact with tumor‐associated antigens (TAAs). Indeed, CAR‐NK cells can be adapted to recognize various antigens, hold higher proliferation capacity, and in vivo persistence, show improved infiltration into the tumors, and the ability to overcome the resistant tumor microenvironment leading to sustained cytotoxicity against tumors. Accumulating evidence from recent in vivo studies rendering CAR‐NK cell anti‐cancer competencies renewed the attention in the context of cancer immunotherapy, as these redirected effector cells can be used in the development of the “off‐the‐shelf” anti‐cancer immunotherapeutic products. In the current review, we focus on the therapeutic efficacy of CAR‐NK cell therapies for treating various human malignancies, including hematological malignancies and solid tumors, and will discuss the recent findings in this regard, with a special focus on animal studies.
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spelling pubmed-84094192021-09-03 CAR‐NK cell in cancer immunotherapy; A promising frontier Marofi, Faroogh Abdul‐Rasheed, Omar F. Rahman, Heshu Sulaiman Budi, Hendrik Setia Jalil, Abduladheem Turki Yumashev, Alexei Valerievich Hassanzadeh, Ali Yazdanifar, Mahboubeh Motavalli, Roza Chartrand, Max Stanley Ahmadi, Majid Cid‐Arreguid, Angel Jarahian, Mostafa Cancer Sci Review Articles Chimeric antigen receptors (CARs) have a unique facet of synthetic biology and offer a paradigm shift in personalized medicine as they can use and redirect the patient's immune cells to attack cancer cells. CAR‐natural killer (NK) cells combine the targeted specificity of antigens with the subsequent intracellular signaling ability of the receptors to increase their anti‐cancer functions. Importantly, CAR‐NK cells can be utilized as universal cell‐based therapy without requiring human leukocyte antigen (HLA) matching or earlier contact with tumor‐associated antigens (TAAs). Indeed, CAR‐NK cells can be adapted to recognize various antigens, hold higher proliferation capacity, and in vivo persistence, show improved infiltration into the tumors, and the ability to overcome the resistant tumor microenvironment leading to sustained cytotoxicity against tumors. Accumulating evidence from recent in vivo studies rendering CAR‐NK cell anti‐cancer competencies renewed the attention in the context of cancer immunotherapy, as these redirected effector cells can be used in the development of the “off‐the‐shelf” anti‐cancer immunotherapeutic products. In the current review, we focus on the therapeutic efficacy of CAR‐NK cell therapies for treating various human malignancies, including hematological malignancies and solid tumors, and will discuss the recent findings in this regard, with a special focus on animal studies. John Wiley and Sons Inc. 2021-07-07 2021-09 /pmc/articles/PMC8409419/ /pubmed/34050690 http://dx.doi.org/10.1111/cas.14993 Text en © 2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Review Articles
Marofi, Faroogh
Abdul‐Rasheed, Omar F.
Rahman, Heshu Sulaiman
Budi, Hendrik Setia
Jalil, Abduladheem Turki
Yumashev, Alexei Valerievich
Hassanzadeh, Ali
Yazdanifar, Mahboubeh
Motavalli, Roza
Chartrand, Max Stanley
Ahmadi, Majid
Cid‐Arreguid, Angel
Jarahian, Mostafa
CAR‐NK cell in cancer immunotherapy; A promising frontier
title CAR‐NK cell in cancer immunotherapy; A promising frontier
title_full CAR‐NK cell in cancer immunotherapy; A promising frontier
title_fullStr CAR‐NK cell in cancer immunotherapy; A promising frontier
title_full_unstemmed CAR‐NK cell in cancer immunotherapy; A promising frontier
title_short CAR‐NK cell in cancer immunotherapy; A promising frontier
title_sort car‐nk cell in cancer immunotherapy; a promising frontier
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8409419/
https://www.ncbi.nlm.nih.gov/pubmed/34050690
http://dx.doi.org/10.1111/cas.14993
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