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Targeting myeloid-derived suppressor cells to enhance natural killer cell-based immunotherapy

Myeloid-derived suppressor cells (MDSCs) are immune cells of the myeloid lineage that progressively accumulate in tumors and play an important role in promoting tumor growth. MDSCs interact with other immune cells present in the tumor microenvironment (TME) and utilize multiple mechanisms to promote...

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Detalles Bibliográficos
Autores principales: Joshi, Shweta, Sharabi, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189042/
https://www.ncbi.nlm.nih.gov/pubmed/35122833
http://dx.doi.org/10.1016/j.pharmthera.2022.108114
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author Joshi, Shweta
Sharabi, Andrew
author_facet Joshi, Shweta
Sharabi, Andrew
author_sort Joshi, Shweta
collection PubMed
description Myeloid-derived suppressor cells (MDSCs) are immune cells of the myeloid lineage that progressively accumulate in tumors and play an important role in promoting tumor growth. MDSCs interact with other immune cells present in the tumor microenvironment (TME) and utilize multiple mechanisms to promote immunosuppression. On the other hand, natural killer (NK) cells are cytotoxic cells of the innate immune system and work as one of the first lines of defense against tumors. However, the role of MDSCs in regulating or suppressing NK cells within the TME is poorly understood. This review discusses MDSC-associated immunosuppression, the mechanisms regulating communication between MDSCs and NK cells in the tumor microenvironment, and how MDSC may impact NK-cell-based immunotherapies. We also explore various strategies to increase NK cell cytotoxicity by blocking MDSC-mediated immunosuppression with the goal of enhancing cell based anticancer therapeutics.
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spelling pubmed-91890422023-07-01 Targeting myeloid-derived suppressor cells to enhance natural killer cell-based immunotherapy Joshi, Shweta Sharabi, Andrew Pharmacol Ther Article Myeloid-derived suppressor cells (MDSCs) are immune cells of the myeloid lineage that progressively accumulate in tumors and play an important role in promoting tumor growth. MDSCs interact with other immune cells present in the tumor microenvironment (TME) and utilize multiple mechanisms to promote immunosuppression. On the other hand, natural killer (NK) cells are cytotoxic cells of the innate immune system and work as one of the first lines of defense against tumors. However, the role of MDSCs in regulating or suppressing NK cells within the TME is poorly understood. This review discusses MDSC-associated immunosuppression, the mechanisms regulating communication between MDSCs and NK cells in the tumor microenvironment, and how MDSC may impact NK-cell-based immunotherapies. We also explore various strategies to increase NK cell cytotoxicity by blocking MDSC-mediated immunosuppression with the goal of enhancing cell based anticancer therapeutics. 2022-07 2022-02-02 /pmc/articles/PMC9189042/ /pubmed/35122833 http://dx.doi.org/10.1016/j.pharmthera.2022.108114 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Joshi, Shweta
Sharabi, Andrew
Targeting myeloid-derived suppressor cells to enhance natural killer cell-based immunotherapy
title Targeting myeloid-derived suppressor cells to enhance natural killer cell-based immunotherapy
title_full Targeting myeloid-derived suppressor cells to enhance natural killer cell-based immunotherapy
title_fullStr Targeting myeloid-derived suppressor cells to enhance natural killer cell-based immunotherapy
title_full_unstemmed Targeting myeloid-derived suppressor cells to enhance natural killer cell-based immunotherapy
title_short Targeting myeloid-derived suppressor cells to enhance natural killer cell-based immunotherapy
title_sort targeting myeloid-derived suppressor cells to enhance natural killer cell-based immunotherapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189042/
https://www.ncbi.nlm.nih.gov/pubmed/35122833
http://dx.doi.org/10.1016/j.pharmthera.2022.108114
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