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Metabolic regulation of NK cell function: implications for immunotherapy

Natural killer (NK) cells are innate immune lymphocytes capable of rapidly responding to tumors and infection without prior sensitization. There is increasing interest and success in harnessing NK cell function for the treatment of disease, in particular cancers. NK cell activation is dependent on i...

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Detalles Bibliográficos
Autores principales: Sohn, Hyogon, Cooper, Megan A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9869966/
https://www.ncbi.nlm.nih.gov/pubmed/36710923
http://dx.doi.org/10.1097/IN9.0000000000000020
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author Sohn, Hyogon
Cooper, Megan A.
author_facet Sohn, Hyogon
Cooper, Megan A.
author_sort Sohn, Hyogon
collection PubMed
description Natural killer (NK) cells are innate immune lymphocytes capable of rapidly responding to tumors and infection without prior sensitization. There is increasing interest and success in harnessing NK cell function for the treatment of disease, in particular cancers. NK cell activation is dependent on integration of signals through cytokine and germline-encoded activating and inhibitory receptors. The availability of metabolic fuels and pathways is required for NK effector functions including proliferation, killing, and production of interferon gamma (IFN-γ). An understanding of NK cell immunometabolism is thus essential for developing immunotherapy approaches that will allow for optimal effector functions in patients. Studies in mice and humans have demonstrated stimulation-dependent metabolic changes that are required for NK cell function. Here we review the most recent findings in NK cell immunometabolism relevant to disease models and translation to therapy of patients.
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spelling pubmed-98699662023-01-27 Metabolic regulation of NK cell function: implications for immunotherapy Sohn, Hyogon Cooper, Megan A. Immunometabolism (Cobham) Mini Review Natural killer (NK) cells are innate immune lymphocytes capable of rapidly responding to tumors and infection without prior sensitization. There is increasing interest and success in harnessing NK cell function for the treatment of disease, in particular cancers. NK cell activation is dependent on integration of signals through cytokine and germline-encoded activating and inhibitory receptors. The availability of metabolic fuels and pathways is required for NK effector functions including proliferation, killing, and production of interferon gamma (IFN-γ). An understanding of NK cell immunometabolism is thus essential for developing immunotherapy approaches that will allow for optimal effector functions in patients. Studies in mice and humans have demonstrated stimulation-dependent metabolic changes that are required for NK cell function. Here we review the most recent findings in NK cell immunometabolism relevant to disease models and translation to therapy of patients. Lippincott Williams & Wilkins 2023-01-23 /pmc/articles/PMC9869966/ /pubmed/36710923 http://dx.doi.org/10.1097/IN9.0000000000000020 Text en Copyright © 2023 The Author(s), Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This paper is published under Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Mini Review
Sohn, Hyogon
Cooper, Megan A.
Metabolic regulation of NK cell function: implications for immunotherapy
title Metabolic regulation of NK cell function: implications for immunotherapy
title_full Metabolic regulation of NK cell function: implications for immunotherapy
title_fullStr Metabolic regulation of NK cell function: implications for immunotherapy
title_full_unstemmed Metabolic regulation of NK cell function: implications for immunotherapy
title_short Metabolic regulation of NK cell function: implications for immunotherapy
title_sort metabolic regulation of nk cell function: implications for immunotherapy
topic Mini Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9869966/
https://www.ncbi.nlm.nih.gov/pubmed/36710923
http://dx.doi.org/10.1097/IN9.0000000000000020
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