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Chimeric antigen receptor-engineered NK cells: new weapons of cancer immunotherapy with great potential
Chimeric antigen receptor (CAR)-engineered T (CAR-T) cells have obtained prominent achievement in the clinical immunotherapy of hematological malignant tumors, leading to a rapid development of cellular immunotherapy in cancer treatment. Scientists are also aware of the prospective advantages of CAR...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9628181/ https://www.ncbi.nlm.nih.gov/pubmed/36324149 http://dx.doi.org/10.1186/s40164-022-00341-7 |
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author | Wang, Xiao Yang, Xuejiao Yuan, Xiang Wang, Wenbo Wang, Yueying |
author_facet | Wang, Xiao Yang, Xuejiao Yuan, Xiang Wang, Wenbo Wang, Yueying |
author_sort | Wang, Xiao |
collection | PubMed |
description | Chimeric antigen receptor (CAR)-engineered T (CAR-T) cells have obtained prominent achievement in the clinical immunotherapy of hematological malignant tumors, leading to a rapid development of cellular immunotherapy in cancer treatment. Scientists are also aware of the prospective advantages of CAR engineering in cellular immunotherapy. Due to various limitations such as the serious side effects of CAR-T therapy, researchers began to investigate other immune cells for CAR modification. Natural killer (NK) cells are critical innate immune cells with the characteristic of non-specifically recognizing target cells and with the potential to become “off-the-shelf” products. In recent years, many preclinical studies on CAR-engineered NK (CAR-NK) cells have shown their remarkable efficacy in cancer therapy and their superiority over autologous CAR-T cells. In this review, we summarize the generation, mechanisms of anti-tumor activity and unique advantages of CAR-NK cells, and then analyze some challenges and recent clinical trials about CAR-NK cells therapy. We believe that CAR-NK therapy is a promising prospect for cancer immunotherapy in the future. |
format | Online Article Text |
id | pubmed-9628181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-96281812022-11-03 Chimeric antigen receptor-engineered NK cells: new weapons of cancer immunotherapy with great potential Wang, Xiao Yang, Xuejiao Yuan, Xiang Wang, Wenbo Wang, Yueying Exp Hematol Oncol Review Chimeric antigen receptor (CAR)-engineered T (CAR-T) cells have obtained prominent achievement in the clinical immunotherapy of hematological malignant tumors, leading to a rapid development of cellular immunotherapy in cancer treatment. Scientists are also aware of the prospective advantages of CAR engineering in cellular immunotherapy. Due to various limitations such as the serious side effects of CAR-T therapy, researchers began to investigate other immune cells for CAR modification. Natural killer (NK) cells are critical innate immune cells with the characteristic of non-specifically recognizing target cells and with the potential to become “off-the-shelf” products. In recent years, many preclinical studies on CAR-engineered NK (CAR-NK) cells have shown their remarkable efficacy in cancer therapy and their superiority over autologous CAR-T cells. In this review, we summarize the generation, mechanisms of anti-tumor activity and unique advantages of CAR-NK cells, and then analyze some challenges and recent clinical trials about CAR-NK cells therapy. We believe that CAR-NK therapy is a promising prospect for cancer immunotherapy in the future. BioMed Central 2022-11-02 /pmc/articles/PMC9628181/ /pubmed/36324149 http://dx.doi.org/10.1186/s40164-022-00341-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Wang, Xiao Yang, Xuejiao Yuan, Xiang Wang, Wenbo Wang, Yueying Chimeric antigen receptor-engineered NK cells: new weapons of cancer immunotherapy with great potential |
title | Chimeric antigen receptor-engineered NK cells: new weapons of cancer immunotherapy with great potential |
title_full | Chimeric antigen receptor-engineered NK cells: new weapons of cancer immunotherapy with great potential |
title_fullStr | Chimeric antigen receptor-engineered NK cells: new weapons of cancer immunotherapy with great potential |
title_full_unstemmed | Chimeric antigen receptor-engineered NK cells: new weapons of cancer immunotherapy with great potential |
title_short | Chimeric antigen receptor-engineered NK cells: new weapons of cancer immunotherapy with great potential |
title_sort | chimeric antigen receptor-engineered nk cells: new weapons of cancer immunotherapy with great potential |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9628181/ https://www.ncbi.nlm.nih.gov/pubmed/36324149 http://dx.doi.org/10.1186/s40164-022-00341-7 |
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