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Chimeric antigen receptor-engineered natural killer cells for cancer immunotherapy
Natural killer (NK) cells are a critical component of the innate immune system. Chimeric antigen receptors (CARs) re-direct NK cells toward tumor cells carrying corresponding antigens, creating major opportunities in the fight against cancer. CAR NK cells have the potential for use as universal CAR ...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720606/ https://www.ncbi.nlm.nih.gov/pubmed/33287875 http://dx.doi.org/10.1186/s13045-020-00998-9 |
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author | Yilmaz, Ahmet Cui, Hanwei Caligiuri, Michael A. Yu, Jianhua |
author_facet | Yilmaz, Ahmet Cui, Hanwei Caligiuri, Michael A. Yu, Jianhua |
author_sort | Yilmaz, Ahmet |
collection | PubMed |
description | Natural killer (NK) cells are a critical component of the innate immune system. Chimeric antigen receptors (CARs) re-direct NK cells toward tumor cells carrying corresponding antigens, creating major opportunities in the fight against cancer. CAR NK cells have the potential for use as universal CAR cells without the need for human leukocyte antigen matching or prior exposure to tumor-associated antigens. Exciting data from recent clinical trials have renewed interest in the field of cancer immunotherapy due to the potential of CAR NK cells in the production of “off-the-shelf” anti-cancer immunotherapeutic products. Here, we provide an up-to-date comprehensive overview of the recent advancements in key areas of CAR NK cell research and identify under-investigated research areas. We summarize improvements in CAR design and structure, advantages and disadvantages of using CAR NK cells as an alternative to CAR T cell therapy, and list sources to obtain NK cells. In addition, we provide a list of tumor-associated antigens targeted by CAR NK cells and detail challenges in expanding and transducing NK cells for CAR production. We additionally discuss barriers to effective treatment and suggest solutions to improve CAR NK cell function, proliferation, persistence, therapeutic effectiveness, and safety in solid and liquid tumors. |
format | Online Article Text |
id | pubmed-7720606 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77206062020-12-08 Chimeric antigen receptor-engineered natural killer cells for cancer immunotherapy Yilmaz, Ahmet Cui, Hanwei Caligiuri, Michael A. Yu, Jianhua J Hematol Oncol Review Natural killer (NK) cells are a critical component of the innate immune system. Chimeric antigen receptors (CARs) re-direct NK cells toward tumor cells carrying corresponding antigens, creating major opportunities in the fight against cancer. CAR NK cells have the potential for use as universal CAR cells without the need for human leukocyte antigen matching or prior exposure to tumor-associated antigens. Exciting data from recent clinical trials have renewed interest in the field of cancer immunotherapy due to the potential of CAR NK cells in the production of “off-the-shelf” anti-cancer immunotherapeutic products. Here, we provide an up-to-date comprehensive overview of the recent advancements in key areas of CAR NK cell research and identify under-investigated research areas. We summarize improvements in CAR design and structure, advantages and disadvantages of using CAR NK cells as an alternative to CAR T cell therapy, and list sources to obtain NK cells. In addition, we provide a list of tumor-associated antigens targeted by CAR NK cells and detail challenges in expanding and transducing NK cells for CAR production. We additionally discuss barriers to effective treatment and suggest solutions to improve CAR NK cell function, proliferation, persistence, therapeutic effectiveness, and safety in solid and liquid tumors. BioMed Central 2020-12-07 /pmc/articles/PMC7720606/ /pubmed/33287875 http://dx.doi.org/10.1186/s13045-020-00998-9 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Yilmaz, Ahmet Cui, Hanwei Caligiuri, Michael A. Yu, Jianhua Chimeric antigen receptor-engineered natural killer cells for cancer immunotherapy |
title | Chimeric antigen receptor-engineered natural killer cells for cancer immunotherapy |
title_full | Chimeric antigen receptor-engineered natural killer cells for cancer immunotherapy |
title_fullStr | Chimeric antigen receptor-engineered natural killer cells for cancer immunotherapy |
title_full_unstemmed | Chimeric antigen receptor-engineered natural killer cells for cancer immunotherapy |
title_short | Chimeric antigen receptor-engineered natural killer cells for cancer immunotherapy |
title_sort | chimeric antigen receptor-engineered natural killer cells for cancer immunotherapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720606/ https://www.ncbi.nlm.nih.gov/pubmed/33287875 http://dx.doi.org/10.1186/s13045-020-00998-9 |
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