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CAR-NK cells for cancer immunotherapy: from bench to bedside

Natural killer (NK) cells are unique innate immune cells and manifest rapid and potent cytotoxicity for cancer immunotherapy and pathogen removal without the requirement of prior sensitization or recognition of peptide antigens. Distinguish from the T lymphocyte-based cythotherapy with toxic side ef...

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Autores principales: Zhang, Leisheng, Meng, Yuan, Feng, Xiaoming, Han, Zhongchao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8932134/
https://www.ncbi.nlm.nih.gov/pubmed/35303962
http://dx.doi.org/10.1186/s40364-022-00364-6
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author Zhang, Leisheng
Meng, Yuan
Feng, Xiaoming
Han, Zhongchao
author_facet Zhang, Leisheng
Meng, Yuan
Feng, Xiaoming
Han, Zhongchao
author_sort Zhang, Leisheng
collection PubMed
description Natural killer (NK) cells are unique innate immune cells and manifest rapid and potent cytotoxicity for cancer immunotherapy and pathogen removal without the requirement of prior sensitization or recognition of peptide antigens. Distinguish from the T lymphocyte-based cythotherapy with toxic side effects, chimeric antigen receptor-transduced NK (CAR-NK) cells are adequate to simultaneously improve efficacy and control adverse effects including acute cytokine release syndrome (CRS), neurotoxicity and graft-versus-host disease (GVHD). Moreover, considering the inherent properties of NK cells, the CAR-NK cells are “off-the-shelf” product satisfying the clinical demand for large-scale manufacture for cancer immunotherapy attribute to the cytotoxic effect via both NK cell receptor-dependent and CAR-dependent signaling cascades. In this review, we mainly focus on the latest updates of CAR-NK cell-based tactics, together with the opportunities and challenges for cancer immunotherapies, which represent the paradigm for boosting the immune system to enhance antitumor responses and ultimately eliminate malignancies. Collectively, we summarize and highlight the auspicious improvement in CAR-NK cells and will benefit the large-scale preclinical and clinical investigations in adoptive immunotherapy.
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spelling pubmed-89321342022-03-23 CAR-NK cells for cancer immunotherapy: from bench to bedside Zhang, Leisheng Meng, Yuan Feng, Xiaoming Han, Zhongchao Biomark Res Review Natural killer (NK) cells are unique innate immune cells and manifest rapid and potent cytotoxicity for cancer immunotherapy and pathogen removal without the requirement of prior sensitization or recognition of peptide antigens. Distinguish from the T lymphocyte-based cythotherapy with toxic side effects, chimeric antigen receptor-transduced NK (CAR-NK) cells are adequate to simultaneously improve efficacy and control adverse effects including acute cytokine release syndrome (CRS), neurotoxicity and graft-versus-host disease (GVHD). Moreover, considering the inherent properties of NK cells, the CAR-NK cells are “off-the-shelf” product satisfying the clinical demand for large-scale manufacture for cancer immunotherapy attribute to the cytotoxic effect via both NK cell receptor-dependent and CAR-dependent signaling cascades. In this review, we mainly focus on the latest updates of CAR-NK cell-based tactics, together with the opportunities and challenges for cancer immunotherapies, which represent the paradigm for boosting the immune system to enhance antitumor responses and ultimately eliminate malignancies. Collectively, we summarize and highlight the auspicious improvement in CAR-NK cells and will benefit the large-scale preclinical and clinical investigations in adoptive immunotherapy. BioMed Central 2022-03-18 /pmc/articles/PMC8932134/ /pubmed/35303962 http://dx.doi.org/10.1186/s40364-022-00364-6 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
Zhang, Leisheng
Meng, Yuan
Feng, Xiaoming
Han, Zhongchao
CAR-NK cells for cancer immunotherapy: from bench to bedside
title CAR-NK cells for cancer immunotherapy: from bench to bedside
title_full CAR-NK cells for cancer immunotherapy: from bench to bedside
title_fullStr CAR-NK cells for cancer immunotherapy: from bench to bedside
title_full_unstemmed CAR-NK cells for cancer immunotherapy: from bench to bedside
title_short CAR-NK cells for cancer immunotherapy: from bench to bedside
title_sort car-nk cells for cancer immunotherapy: from bench to bedside
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8932134/
https://www.ncbi.nlm.nih.gov/pubmed/35303962
http://dx.doi.org/10.1186/s40364-022-00364-6
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