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Very‐low‐carbohydrate diet enhances human T‐cell immunity through immunometabolic reprogramming

Very‐low‐carbohydrate diet triggers the endogenous production of ketone bodies as alternative energy substrates. There are as yet unproven assumptions that ketone bodies positively affect human immunity. We have investigated this topic in an in vitro model using primary human T cells and in an immun...

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Autores principales: Hirschberger, Simon, Strauß, Gabriele, Effinger, David, Marstaller, Xaver, Ferstl, Alicia, Müller, Martin B, Wu, Tingting, Hübner, Max, Rahmel, Tim, Mascolo, Hannah, Exner, Nicole, Heß, Julia, Kreth, Friedrich W, Unger, Kristian, Kreth, Simone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8350890/
https://www.ncbi.nlm.nih.gov/pubmed/34151532
http://dx.doi.org/10.15252/emmm.202114323
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author Hirschberger, Simon
Strauß, Gabriele
Effinger, David
Marstaller, Xaver
Ferstl, Alicia
Müller, Martin B
Wu, Tingting
Hübner, Max
Rahmel, Tim
Mascolo, Hannah
Exner, Nicole
Heß, Julia
Kreth, Friedrich W
Unger, Kristian
Kreth, Simone
author_facet Hirschberger, Simon
Strauß, Gabriele
Effinger, David
Marstaller, Xaver
Ferstl, Alicia
Müller, Martin B
Wu, Tingting
Hübner, Max
Rahmel, Tim
Mascolo, Hannah
Exner, Nicole
Heß, Julia
Kreth, Friedrich W
Unger, Kristian
Kreth, Simone
author_sort Hirschberger, Simon
collection PubMed
description Very‐low‐carbohydrate diet triggers the endogenous production of ketone bodies as alternative energy substrates. There are as yet unproven assumptions that ketone bodies positively affect human immunity. We have investigated this topic in an in vitro model using primary human T cells and in an immuno‐nutritional intervention study enrolling healthy volunteers. We show that ketone bodies profoundly impact human T‐cell responses. CD4(+), CD8(+), and regulatory T‐cell capacity were markedly enhanced, and T memory cell formation was augmented. RNAseq and functional metabolic analyses revealed a fundamental immunometabolic reprogramming in response to ketones favoring mitochondrial oxidative metabolism. This confers superior respiratory reserve, cellular energy supply, and reactive oxygen species signaling. Our data suggest a very‐low‐carbohydrate diet as a clinical tool to improve human T‐cell immunity. Rethinking the value of nutrition and dietary interventions in modern medicine is required.
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spelling pubmed-83508902021-08-15 Very‐low‐carbohydrate diet enhances human T‐cell immunity through immunometabolic reprogramming Hirschberger, Simon Strauß, Gabriele Effinger, David Marstaller, Xaver Ferstl, Alicia Müller, Martin B Wu, Tingting Hübner, Max Rahmel, Tim Mascolo, Hannah Exner, Nicole Heß, Julia Kreth, Friedrich W Unger, Kristian Kreth, Simone EMBO Mol Med Articles Very‐low‐carbohydrate diet triggers the endogenous production of ketone bodies as alternative energy substrates. There are as yet unproven assumptions that ketone bodies positively affect human immunity. We have investigated this topic in an in vitro model using primary human T cells and in an immuno‐nutritional intervention study enrolling healthy volunteers. We show that ketone bodies profoundly impact human T‐cell responses. CD4(+), CD8(+), and regulatory T‐cell capacity were markedly enhanced, and T memory cell formation was augmented. RNAseq and functional metabolic analyses revealed a fundamental immunometabolic reprogramming in response to ketones favoring mitochondrial oxidative metabolism. This confers superior respiratory reserve, cellular energy supply, and reactive oxygen species signaling. Our data suggest a very‐low‐carbohydrate diet as a clinical tool to improve human T‐cell immunity. Rethinking the value of nutrition and dietary interventions in modern medicine is required. John Wiley and Sons Inc. 2021-06-21 2021-08-09 /pmc/articles/PMC8350890/ /pubmed/34151532 http://dx.doi.org/10.15252/emmm.202114323 Text en © 2021 The Authors. Published under the terms of the CC BY 4.0 license https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Hirschberger, Simon
Strauß, Gabriele
Effinger, David
Marstaller, Xaver
Ferstl, Alicia
Müller, Martin B
Wu, Tingting
Hübner, Max
Rahmel, Tim
Mascolo, Hannah
Exner, Nicole
Heß, Julia
Kreth, Friedrich W
Unger, Kristian
Kreth, Simone
Very‐low‐carbohydrate diet enhances human T‐cell immunity through immunometabolic reprogramming
title Very‐low‐carbohydrate diet enhances human T‐cell immunity through immunometabolic reprogramming
title_full Very‐low‐carbohydrate diet enhances human T‐cell immunity through immunometabolic reprogramming
title_fullStr Very‐low‐carbohydrate diet enhances human T‐cell immunity through immunometabolic reprogramming
title_full_unstemmed Very‐low‐carbohydrate diet enhances human T‐cell immunity through immunometabolic reprogramming
title_short Very‐low‐carbohydrate diet enhances human T‐cell immunity through immunometabolic reprogramming
title_sort very‐low‐carbohydrate diet enhances human t‐cell immunity through immunometabolic reprogramming
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8350890/
https://www.ncbi.nlm.nih.gov/pubmed/34151532
http://dx.doi.org/10.15252/emmm.202114323
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