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Chimeric antigen receptor engineered natural killer cells for cancer therapy

Natural killer (NK) cells, a unique component of the innate immune system, are inherent killers of stressed and transformed cells. Based on their potent capacity to kill cancer cells and good tolerance of healthy cells, NK cells have been successfully employed in adoptive cell therapy to treat cance...

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Autores principales: Zhang, Yalan, Zhou, Weilin, Yang, Jiangping, Yang, Jinrong, Wang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10413722/
https://www.ncbi.nlm.nih.gov/pubmed/37563648
http://dx.doi.org/10.1186/s40164-023-00431-0
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author Zhang, Yalan
Zhou, Weilin
Yang, Jiangping
Yang, Jinrong
Wang, Wei
author_facet Zhang, Yalan
Zhou, Weilin
Yang, Jiangping
Yang, Jinrong
Wang, Wei
author_sort Zhang, Yalan
collection PubMed
description Natural killer (NK) cells, a unique component of the innate immune system, are inherent killers of stressed and transformed cells. Based on their potent capacity to kill cancer cells and good tolerance of healthy cells, NK cells have been successfully employed in adoptive cell therapy to treat cancer patients. In recent years, the clinical success of chimeric antigen receptor (CAR)-T cells has proven the vast potential of gene-manipulated immune cells as the main force to fight cancer. Following the lessons learned from mature gene-transfer technologies and advanced strategies in CAR-T therapy, NK cells have been rapidly explored as a promising candidate for CAR-based therapy. An exponentially growing number of studies have employed multiple sources of CAR-NK cells to target a wide range of cancer-related antigens, showing remarkable outcomes and encouraging safety profiles. Clinical trials of CAR-NK cells have also shown their impressive therapeutic efficacy in the treatment of hematological tumors, but CAR-NK cell therapy for solid tumors is still in the initial stages. In this review, we present the favorable profile of NK cells as a potential platform for CAR-based engineering and then summarize the outcomes and strategies of CAR-NK therapies in up-to-date preclinical and clinical investigations. Finally, we evaluate the challenges remaining in CAR-NK therapy and describe existing strategies that can assist us in devising future prospective solutions.
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spelling pubmed-104137222023-08-11 Chimeric antigen receptor engineered natural killer cells for cancer therapy Zhang, Yalan Zhou, Weilin Yang, Jiangping Yang, Jinrong Wang, Wei Exp Hematol Oncol Review Natural killer (NK) cells, a unique component of the innate immune system, are inherent killers of stressed and transformed cells. Based on their potent capacity to kill cancer cells and good tolerance of healthy cells, NK cells have been successfully employed in adoptive cell therapy to treat cancer patients. In recent years, the clinical success of chimeric antigen receptor (CAR)-T cells has proven the vast potential of gene-manipulated immune cells as the main force to fight cancer. Following the lessons learned from mature gene-transfer technologies and advanced strategies in CAR-T therapy, NK cells have been rapidly explored as a promising candidate for CAR-based therapy. An exponentially growing number of studies have employed multiple sources of CAR-NK cells to target a wide range of cancer-related antigens, showing remarkable outcomes and encouraging safety profiles. Clinical trials of CAR-NK cells have also shown their impressive therapeutic efficacy in the treatment of hematological tumors, but CAR-NK cell therapy for solid tumors is still in the initial stages. In this review, we present the favorable profile of NK cells as a potential platform for CAR-based engineering and then summarize the outcomes and strategies of CAR-NK therapies in up-to-date preclinical and clinical investigations. Finally, we evaluate the challenges remaining in CAR-NK therapy and describe existing strategies that can assist us in devising future prospective solutions. BioMed Central 2023-08-10 /pmc/articles/PMC10413722/ /pubmed/37563648 http://dx.doi.org/10.1186/s40164-023-00431-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Zhang, Yalan
Zhou, Weilin
Yang, Jiangping
Yang, Jinrong
Wang, Wei
Chimeric antigen receptor engineered natural killer cells for cancer therapy
title Chimeric antigen receptor engineered natural killer cells for cancer therapy
title_full Chimeric antigen receptor engineered natural killer cells for cancer therapy
title_fullStr Chimeric antigen receptor engineered natural killer cells for cancer therapy
title_full_unstemmed Chimeric antigen receptor engineered natural killer cells for cancer therapy
title_short Chimeric antigen receptor engineered natural killer cells for cancer therapy
title_sort chimeric antigen receptor engineered natural killer cells for cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10413722/
https://www.ncbi.nlm.nih.gov/pubmed/37563648
http://dx.doi.org/10.1186/s40164-023-00431-0
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