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Immunosuppressive effects of circulating bile acids in human endotoxemia and septic shock: patients with liver failure are at risk
BACKGROUND: Sepsis-induced immunosuppression is a frequent cause of opportunistic infections and death in critically ill patients. A better understanding of the underlying mechanisms is needed to develop targeted therapies. Circulating bile acids with immunosuppressive effects were recently identifi...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523742/ https://www.ncbi.nlm.nih.gov/pubmed/37759239 http://dx.doi.org/10.1186/s13054-023-04620-5 |
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author | Leonhardt, Julia Dorresteijn, Mirrin J. Neugebauer, Sophie Mihaylov, Diana Kunze, Julia Rubio, Ignacio Hohberger, Frank-Stephan Leonhardt, Silke Kiehntopf, Michael Stahl, Klaus Bode, Christian David, Sascha Wagener, Frank A. D. T. G. Pickkers, Peter Bauer, Michael |
author_facet | Leonhardt, Julia Dorresteijn, Mirrin J. Neugebauer, Sophie Mihaylov, Diana Kunze, Julia Rubio, Ignacio Hohberger, Frank-Stephan Leonhardt, Silke Kiehntopf, Michael Stahl, Klaus Bode, Christian David, Sascha Wagener, Frank A. D. T. G. Pickkers, Peter Bauer, Michael |
author_sort | Leonhardt, Julia |
collection | PubMed |
description | BACKGROUND: Sepsis-induced immunosuppression is a frequent cause of opportunistic infections and death in critically ill patients. A better understanding of the underlying mechanisms is needed to develop targeted therapies. Circulating bile acids with immunosuppressive effects were recently identified in critically ill patients. These bile acids activate the monocyte G-protein coupled receptor TGR5, thereby inducing profound innate immune dysfunction. Whether these mechanisms contribute to immunosuppression and disease severity in sepsis is unknown. The aim of this study was to determine if immunosuppressive bile acids are present in endotoxemia and septic shock and, if so, which patients are particularly at risk. METHODS: To induce experimental endotoxemia in humans, ten healthy volunteers received 2 ng/kg E. coli lipopolysaccharide (LPS). Circulating bile acids were profiled before and after LPS administration. Furthermore, 48 patients with early (shock onset within < 24 h) and severe septic shock (norepinephrine dose > 0.4 μg/kg/min) and 48 healthy age- and sex-matched controls were analyzed for circulating bile acids. To screen for immunosuppressive effects of circulating bile acids, the capability to induce TGR5 activation was computed for each individual bile acid profile by a recently published formula. RESULTS: Although experimental endotoxemia as well as septic shock led to significant increases in total bile acids compared to controls, this increase was mild in most cases. By contrast, there was a marked and significant increase in circulating bile acids in septic shock patients with severe liver failure compared to healthy controls (61.8 µmol/L vs. 2.8 µmol/L, p = 0.0016). Circulating bile acids in these patients were capable to induce immunosuppression, as indicated by a significant increase in TGR5 activation by circulating bile acids (20.4% in severe liver failure vs. 2.8% in healthy controls, p = 0.0139). CONCLUSIONS: Circulating bile acids capable of inducing immunosuppression are present in septic shock patients with severe liver failure. Future studies should examine whether modulation of bile acid metabolism can improve the clinical course and outcome of sepsis in these patients. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-10523742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105237422023-09-28 Immunosuppressive effects of circulating bile acids in human endotoxemia and septic shock: patients with liver failure are at risk Leonhardt, Julia Dorresteijn, Mirrin J. Neugebauer, Sophie Mihaylov, Diana Kunze, Julia Rubio, Ignacio Hohberger, Frank-Stephan Leonhardt, Silke Kiehntopf, Michael Stahl, Klaus Bode, Christian David, Sascha Wagener, Frank A. D. T. G. Pickkers, Peter Bauer, Michael Crit Care Research BACKGROUND: Sepsis-induced immunosuppression is a frequent cause of opportunistic infections and death in critically ill patients. A better understanding of the underlying mechanisms is needed to develop targeted therapies. Circulating bile acids with immunosuppressive effects were recently identified in critically ill patients. These bile acids activate the monocyte G-protein coupled receptor TGR5, thereby inducing profound innate immune dysfunction. Whether these mechanisms contribute to immunosuppression and disease severity in sepsis is unknown. The aim of this study was to determine if immunosuppressive bile acids are present in endotoxemia and septic shock and, if so, which patients are particularly at risk. METHODS: To induce experimental endotoxemia in humans, ten healthy volunteers received 2 ng/kg E. coli lipopolysaccharide (LPS). Circulating bile acids were profiled before and after LPS administration. Furthermore, 48 patients with early (shock onset within < 24 h) and severe septic shock (norepinephrine dose > 0.4 μg/kg/min) and 48 healthy age- and sex-matched controls were analyzed for circulating bile acids. To screen for immunosuppressive effects of circulating bile acids, the capability to induce TGR5 activation was computed for each individual bile acid profile by a recently published formula. RESULTS: Although experimental endotoxemia as well as septic shock led to significant increases in total bile acids compared to controls, this increase was mild in most cases. By contrast, there was a marked and significant increase in circulating bile acids in septic shock patients with severe liver failure compared to healthy controls (61.8 µmol/L vs. 2.8 µmol/L, p = 0.0016). Circulating bile acids in these patients were capable to induce immunosuppression, as indicated by a significant increase in TGR5 activation by circulating bile acids (20.4% in severe liver failure vs. 2.8% in healthy controls, p = 0.0139). CONCLUSIONS: Circulating bile acids capable of inducing immunosuppression are present in septic shock patients with severe liver failure. Future studies should examine whether modulation of bile acid metabolism can improve the clinical course and outcome of sepsis in these patients. GRAPHICAL ABSTRACT: [Image: see text] BioMed Central 2023-09-27 /pmc/articles/PMC10523742/ /pubmed/37759239 http://dx.doi.org/10.1186/s13054-023-04620-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Leonhardt, Julia Dorresteijn, Mirrin J. Neugebauer, Sophie Mihaylov, Diana Kunze, Julia Rubio, Ignacio Hohberger, Frank-Stephan Leonhardt, Silke Kiehntopf, Michael Stahl, Klaus Bode, Christian David, Sascha Wagener, Frank A. D. T. G. Pickkers, Peter Bauer, Michael Immunosuppressive effects of circulating bile acids in human endotoxemia and septic shock: patients with liver failure are at risk |
title | Immunosuppressive effects of circulating bile acids in human endotoxemia and septic shock: patients with liver failure are at risk |
title_full | Immunosuppressive effects of circulating bile acids in human endotoxemia and septic shock: patients with liver failure are at risk |
title_fullStr | Immunosuppressive effects of circulating bile acids in human endotoxemia and septic shock: patients with liver failure are at risk |
title_full_unstemmed | Immunosuppressive effects of circulating bile acids in human endotoxemia and septic shock: patients with liver failure are at risk |
title_short | Immunosuppressive effects of circulating bile acids in human endotoxemia and septic shock: patients with liver failure are at risk |
title_sort | immunosuppressive effects of circulating bile acids in human endotoxemia and septic shock: patients with liver failure are at risk |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523742/ https://www.ncbi.nlm.nih.gov/pubmed/37759239 http://dx.doi.org/10.1186/s13054-023-04620-5 |
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