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Effects of PD-1 Signaling on Immunometabolic Reprogramming

Programmed Death-1 (PD-1; CD279) is an inhibitory receptor induced in several activated immune cells and, after engagement with its ligands PD-L1 and PD-L2, serves as a key mediator of peripheral tolerance. However, PD-1 signaling also has detrimental effects on T cell function by posing breaks on a...

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Detalles Bibliográficos
Autores principales: Boussiotis, Vassiliki A., Patsoukis, Nikolaos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975241/
https://www.ncbi.nlm.nih.gov/pubmed/35371563
http://dx.doi.org/10.20900/immunometab20220007
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author Boussiotis, Vassiliki A.
Patsoukis, Nikolaos
author_facet Boussiotis, Vassiliki A.
Patsoukis, Nikolaos
author_sort Boussiotis, Vassiliki A.
collection PubMed
description Programmed Death-1 (PD-1; CD279) is an inhibitory receptor induced in several activated immune cells and, after engagement with its ligands PD-L1 and PD-L2, serves as a key mediator of peripheral tolerance. However, PD-1 signaling also has detrimental effects on T cell function by posing breaks on antitumor and antiviral immunity. PD-1 blocking immunotherapy either alone or in combination with other therapeutic modalities has shown great promise in cancer treatment. However, it is unclear why only a small fraction of patients responds to this type of therapy. For this reason, efforts to better understand the mechanisms of PD-1 function have recently been intensified, with the goal to reveal new strategies to overcome current limitations. The signaling pathways that are inhibited by PD-1 impact key regulators of metabolism. Here, we provide an overview of the current knowledge about the effects of PD-1 on metabolic reprogramming of immune cells and their consequences on systemic metabolism.
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spelling pubmed-89752412022-04-01 Effects of PD-1 Signaling on Immunometabolic Reprogramming Boussiotis, Vassiliki A. Patsoukis, Nikolaos Immunometabolism Article Programmed Death-1 (PD-1; CD279) is an inhibitory receptor induced in several activated immune cells and, after engagement with its ligands PD-L1 and PD-L2, serves as a key mediator of peripheral tolerance. However, PD-1 signaling also has detrimental effects on T cell function by posing breaks on antitumor and antiviral immunity. PD-1 blocking immunotherapy either alone or in combination with other therapeutic modalities has shown great promise in cancer treatment. However, it is unclear why only a small fraction of patients responds to this type of therapy. For this reason, efforts to better understand the mechanisms of PD-1 function have recently been intensified, with the goal to reveal new strategies to overcome current limitations. The signaling pathways that are inhibited by PD-1 impact key regulators of metabolism. Here, we provide an overview of the current knowledge about the effects of PD-1 on metabolic reprogramming of immune cells and their consequences on systemic metabolism. 2022 2022-03-10 /pmc/articles/PMC8975241/ /pubmed/35371563 http://dx.doi.org/10.20900/immunometab20220007 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms and conditions of Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Boussiotis, Vassiliki A.
Patsoukis, Nikolaos
Effects of PD-1 Signaling on Immunometabolic Reprogramming
title Effects of PD-1 Signaling on Immunometabolic Reprogramming
title_full Effects of PD-1 Signaling on Immunometabolic Reprogramming
title_fullStr Effects of PD-1 Signaling on Immunometabolic Reprogramming
title_full_unstemmed Effects of PD-1 Signaling on Immunometabolic Reprogramming
title_short Effects of PD-1 Signaling on Immunometabolic Reprogramming
title_sort effects of pd-1 signaling on immunometabolic reprogramming
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975241/
https://www.ncbi.nlm.nih.gov/pubmed/35371563
http://dx.doi.org/10.20900/immunometab20220007
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