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Natural killer cell immunotherapy in glioblastoma
Glioblastoma (GBM) is one of the most difficult cancers to treat because GBM has the high therapeutic resistance. Recently, immunotherapies for GBM have been used instead of conventional treatments. Among them, Natural killer (NK) cell-based immunotherapy has the potential to treat GBM due to its pr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616998/ https://www.ncbi.nlm.nih.gov/pubmed/36305981 http://dx.doi.org/10.1007/s12672-022-00567-1 |
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author | Hosseinalizadeh, Hamed Habibi Roudkenar, Mehryar Mohammadi Roushandeh, Amaneh Kuwahara, Yoshikazu Tomita, Kazuo Sato, Tomoaki |
author_facet | Hosseinalizadeh, Hamed Habibi Roudkenar, Mehryar Mohammadi Roushandeh, Amaneh Kuwahara, Yoshikazu Tomita, Kazuo Sato, Tomoaki |
author_sort | Hosseinalizadeh, Hamed |
collection | PubMed |
description | Glioblastoma (GBM) is one of the most difficult cancers to treat because GBM has the high therapeutic resistance. Recently, immunotherapies for GBM have been used instead of conventional treatments. Among them, Natural killer (NK) cell-based immunotherapy has the potential to treat GBM due to its properties such as the absence of restriction by antigen-antibody reaction and deep penetration into the tumor microenvironment. Especially, genetically engineered NK cells, such as chimeric antigen receptor (CAR)-NK cells, dual antigen-targeting CAR NK cells, and adapter chimeric antigen receptor NK cells are considered to be an important tool for GBM immunotherapy. Therefore, this review describes the recent efforts of NK cell-based immunotherapy in GBM patients. We also describe key receptors expressing on NK cells such as killer cell immunoglobulin-like receptor, CD16, and natural killer group 2, member D (NKG2DL) receptor and discuss the function and importance of these molecules. |
format | Online Article Text |
id | pubmed-9616998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-96169982022-10-30 Natural killer cell immunotherapy in glioblastoma Hosseinalizadeh, Hamed Habibi Roudkenar, Mehryar Mohammadi Roushandeh, Amaneh Kuwahara, Yoshikazu Tomita, Kazuo Sato, Tomoaki Discov Oncol Review Glioblastoma (GBM) is one of the most difficult cancers to treat because GBM has the high therapeutic resistance. Recently, immunotherapies for GBM have been used instead of conventional treatments. Among them, Natural killer (NK) cell-based immunotherapy has the potential to treat GBM due to its properties such as the absence of restriction by antigen-antibody reaction and deep penetration into the tumor microenvironment. Especially, genetically engineered NK cells, such as chimeric antigen receptor (CAR)-NK cells, dual antigen-targeting CAR NK cells, and adapter chimeric antigen receptor NK cells are considered to be an important tool for GBM immunotherapy. Therefore, this review describes the recent efforts of NK cell-based immunotherapy in GBM patients. We also describe key receptors expressing on NK cells such as killer cell immunoglobulin-like receptor, CD16, and natural killer group 2, member D (NKG2DL) receptor and discuss the function and importance of these molecules. Springer US 2022-10-28 /pmc/articles/PMC9616998/ /pubmed/36305981 http://dx.doi.org/10.1007/s12672-022-00567-1 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/) . |
spellingShingle | Review Hosseinalizadeh, Hamed Habibi Roudkenar, Mehryar Mohammadi Roushandeh, Amaneh Kuwahara, Yoshikazu Tomita, Kazuo Sato, Tomoaki Natural killer cell immunotherapy in glioblastoma |
title | Natural killer cell immunotherapy in glioblastoma |
title_full | Natural killer cell immunotherapy in glioblastoma |
title_fullStr | Natural killer cell immunotherapy in glioblastoma |
title_full_unstemmed | Natural killer cell immunotherapy in glioblastoma |
title_short | Natural killer cell immunotherapy in glioblastoma |
title_sort | natural killer cell immunotherapy in glioblastoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616998/ https://www.ncbi.nlm.nih.gov/pubmed/36305981 http://dx.doi.org/10.1007/s12672-022-00567-1 |
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