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Ketone Bodies Improve Human CD8(+) Cytotoxic T-Cell Immune Response During COVID-19 Infection
Severe COVID-19 is characterized by profound CD8(+) T-cell dysfunction, which cannot be specifically treated to date. We here investigate whether metabolic CD8(+) T-cell reprogramming by ketone bodies could be a promising strategy to overcome the immunoparalysis in COVID-19 patients. This approach w...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9243504/ https://www.ncbi.nlm.nih.gov/pubmed/35783654 http://dx.doi.org/10.3389/fmed.2022.923502 |
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author | Hirschberger, Simon Gellert, Luca Effinger, David Muenchhoff, Maximilian Herrmann, Markus Briegel, Josef-Maria Zwißler, Bernhard Kreth, Simone |
author_facet | Hirschberger, Simon Gellert, Luca Effinger, David Muenchhoff, Maximilian Herrmann, Markus Briegel, Josef-Maria Zwißler, Bernhard Kreth, Simone |
author_sort | Hirschberger, Simon |
collection | PubMed |
description | Severe COVID-19 is characterized by profound CD8(+) T-cell dysfunction, which cannot be specifically treated to date. We here investigate whether metabolic CD8(+) T-cell reprogramming by ketone bodies could be a promising strategy to overcome the immunoparalysis in COVID-19 patients. This approach was triggered by our recent pioneering study, which has provided evidence that CD8(+) T-cell capacity in healthy subjects could be significantly empowered by a Ketogenic Diet. These improvements were achieved by immunometabolic rewiring toward oxidative phosphorylation. We here report similar strengthening of CD8(+) T cells obtained from severely diseased COVID-19 patients: Flow cytometry and ELISA revealed elevated cytokine expression and secretion (up to + 24%) upon ketone treatment and enhanced cell lysis capacity (+ 21%). Metabolic analyses using Seahorse technology revealed upregulated mitochondrial respiratory chain activity (+ 25%), enabling both superior energy supply (+ 44%) and higher mitochondrial reactive oxygen species signaling. These beneficial effects of ketones might represent evolutionary conserved mechanisms to strengthen human immunity. Our findings pave the road for metabolic treatment studies in COVID-19. |
format | Online Article Text |
id | pubmed-9243504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92435042022-07-01 Ketone Bodies Improve Human CD8(+) Cytotoxic T-Cell Immune Response During COVID-19 Infection Hirschberger, Simon Gellert, Luca Effinger, David Muenchhoff, Maximilian Herrmann, Markus Briegel, Josef-Maria Zwißler, Bernhard Kreth, Simone Front Med (Lausanne) Medicine Severe COVID-19 is characterized by profound CD8(+) T-cell dysfunction, which cannot be specifically treated to date. We here investigate whether metabolic CD8(+) T-cell reprogramming by ketone bodies could be a promising strategy to overcome the immunoparalysis in COVID-19 patients. This approach was triggered by our recent pioneering study, which has provided evidence that CD8(+) T-cell capacity in healthy subjects could be significantly empowered by a Ketogenic Diet. These improvements were achieved by immunometabolic rewiring toward oxidative phosphorylation. We here report similar strengthening of CD8(+) T cells obtained from severely diseased COVID-19 patients: Flow cytometry and ELISA revealed elevated cytokine expression and secretion (up to + 24%) upon ketone treatment and enhanced cell lysis capacity (+ 21%). Metabolic analyses using Seahorse technology revealed upregulated mitochondrial respiratory chain activity (+ 25%), enabling both superior energy supply (+ 44%) and higher mitochondrial reactive oxygen species signaling. These beneficial effects of ketones might represent evolutionary conserved mechanisms to strengthen human immunity. Our findings pave the road for metabolic treatment studies in COVID-19. Frontiers Media S.A. 2022-06-16 /pmc/articles/PMC9243504/ /pubmed/35783654 http://dx.doi.org/10.3389/fmed.2022.923502 Text en Copyright © 2022 Hirschberger, Gellert, Effinger, Muenchhoff, Herrmann, Briegel, Zwißler and Kreth. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Hirschberger, Simon Gellert, Luca Effinger, David Muenchhoff, Maximilian Herrmann, Markus Briegel, Josef-Maria Zwißler, Bernhard Kreth, Simone Ketone Bodies Improve Human CD8(+) Cytotoxic T-Cell Immune Response During COVID-19 Infection |
title | Ketone Bodies Improve Human CD8(+) Cytotoxic T-Cell Immune Response During COVID-19 Infection |
title_full | Ketone Bodies Improve Human CD8(+) Cytotoxic T-Cell Immune Response During COVID-19 Infection |
title_fullStr | Ketone Bodies Improve Human CD8(+) Cytotoxic T-Cell Immune Response During COVID-19 Infection |
title_full_unstemmed | Ketone Bodies Improve Human CD8(+) Cytotoxic T-Cell Immune Response During COVID-19 Infection |
title_short | Ketone Bodies Improve Human CD8(+) Cytotoxic T-Cell Immune Response During COVID-19 Infection |
title_sort | ketone bodies improve human cd8(+) cytotoxic t-cell immune response during covid-19 infection |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9243504/ https://www.ncbi.nlm.nih.gov/pubmed/35783654 http://dx.doi.org/10.3389/fmed.2022.923502 |
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