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Natural killer cells: a promising immunotherapy for cancer
As a promising alternative platform for cellular immunotherapy, natural killer cells (NK) have recently gained attention as an important type of innate immune regulatory cell. NK cells can rapidly kill multiple adjacent cancer cells through non-MHC-restrictive effects. Although tumors may develop mu...
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/PMC9125849/ https://www.ncbi.nlm.nih.gov/pubmed/35606854 http://dx.doi.org/10.1186/s12967-022-03437-0 |
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author | Chu, Junfeng Gao, Fengcai Yan, Meimei Zhao, Shuang Yan, Zheng Shi, Bian Liu, Yanyan |
author_facet | Chu, Junfeng Gao, Fengcai Yan, Meimei Zhao, Shuang Yan, Zheng Shi, Bian Liu, Yanyan |
author_sort | Chu, Junfeng |
collection | PubMed |
description | As a promising alternative platform for cellular immunotherapy, natural killer cells (NK) have recently gained attention as an important type of innate immune regulatory cell. NK cells can rapidly kill multiple adjacent cancer cells through non-MHC-restrictive effects. Although tumors may develop multiple resistance mechanisms to endogenous NK cell attack, in vitro activation, expansion, and genetic modification of NK cells can greatly enhance their anti-tumor activity and give them the ability to overcome drug resistance. Some of these approaches have been translated into clinical applications, and clinical trials of NK cell infusion in patients with hematological malignancies and solid tumors have thus far yielded many encouraging clinical results. CAR-T cells have exhibited great success in treating hematological malignancies, but their drawbacks include high manufacturing costs and potentially fatal toxicity, such as cytokine release syndrome. To overcome these issues, CAR-NK cells were generated through genetic engineering and demonstrated significant clinical responses and lower adverse effects compared with CAR-T cell therapy. In this review, we summarize recent advances in NK cell immunotherapy, focusing on NK cell biology and function, the types of NK cell therapy, and clinical trials and future perspectives on NK cell therapy. |
format | Online Article Text |
id | pubmed-9125849 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91258492022-05-24 Natural killer cells: a promising immunotherapy for cancer Chu, Junfeng Gao, Fengcai Yan, Meimei Zhao, Shuang Yan, Zheng Shi, Bian Liu, Yanyan J Transl Med Review As a promising alternative platform for cellular immunotherapy, natural killer cells (NK) have recently gained attention as an important type of innate immune regulatory cell. NK cells can rapidly kill multiple adjacent cancer cells through non-MHC-restrictive effects. Although tumors may develop multiple resistance mechanisms to endogenous NK cell attack, in vitro activation, expansion, and genetic modification of NK cells can greatly enhance their anti-tumor activity and give them the ability to overcome drug resistance. Some of these approaches have been translated into clinical applications, and clinical trials of NK cell infusion in patients with hematological malignancies and solid tumors have thus far yielded many encouraging clinical results. CAR-T cells have exhibited great success in treating hematological malignancies, but their drawbacks include high manufacturing costs and potentially fatal toxicity, such as cytokine release syndrome. To overcome these issues, CAR-NK cells were generated through genetic engineering and demonstrated significant clinical responses and lower adverse effects compared with CAR-T cell therapy. In this review, we summarize recent advances in NK cell immunotherapy, focusing on NK cell biology and function, the types of NK cell therapy, and clinical trials and future perspectives on NK cell therapy. BioMed Central 2022-05-23 /pmc/articles/PMC9125849/ /pubmed/35606854 http://dx.doi.org/10.1186/s12967-022-03437-0 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 Chu, Junfeng Gao, Fengcai Yan, Meimei Zhao, Shuang Yan, Zheng Shi, Bian Liu, Yanyan Natural killer cells: a promising immunotherapy for cancer |
title | Natural killer cells: a promising immunotherapy for cancer |
title_full | Natural killer cells: a promising immunotherapy for cancer |
title_fullStr | Natural killer cells: a promising immunotherapy for cancer |
title_full_unstemmed | Natural killer cells: a promising immunotherapy for cancer |
title_short | Natural killer cells: a promising immunotherapy for cancer |
title_sort | natural killer cells: a promising immunotherapy for cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9125849/ https://www.ncbi.nlm.nih.gov/pubmed/35606854 http://dx.doi.org/10.1186/s12967-022-03437-0 |
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