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The Neuroimmune Response to Surgery – An Exploratory Study of Trauma-Induced Changes in Innate Immunity and Heart Rate Variability

Surgery triggers a systemic inflammatory response that ultimately impacts the brain and associates with long-term cognitive impairment. Adequate regulation of this immune surge is pivotal for a successful surgical recovery. We explored the temporal immune response in a surgical cohort and its associ...

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Autores principales: Hildenborg, Malin, Kåhlin, Jessica, Granath, Fredrik, Schening, Anna, Granström, Anna, Ebberyd, Anette, Klevenvall, Lena, Zetterberg, Henrik, Han, Jinming, Schlegel, Todd T., Harris, Robert, Harris, Helena Erlandsson, Eriksson, Lars I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9301672/
https://www.ncbi.nlm.nih.gov/pubmed/35874666
http://dx.doi.org/10.3389/fimmu.2022.911744
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author Hildenborg, Malin
Kåhlin, Jessica
Granath, Fredrik
Schening, Anna
Granström, Anna
Ebberyd, Anette
Klevenvall, Lena
Zetterberg, Henrik
Han, Jinming
Schlegel, Todd T.
Harris, Robert
Harris, Helena Erlandsson
Eriksson, Lars I.
author_facet Hildenborg, Malin
Kåhlin, Jessica
Granath, Fredrik
Schening, Anna
Granström, Anna
Ebberyd, Anette
Klevenvall, Lena
Zetterberg, Henrik
Han, Jinming
Schlegel, Todd T.
Harris, Robert
Harris, Helena Erlandsson
Eriksson, Lars I.
author_sort Hildenborg, Malin
collection PubMed
description Surgery triggers a systemic inflammatory response that ultimately impacts the brain and associates with long-term cognitive impairment. Adequate regulation of this immune surge is pivotal for a successful surgical recovery. We explored the temporal immune response in a surgical cohort and its associations with neuroimmune regulatory pathways and cognition, in keeping with the growing body of evidence pointing towards the brain as a regulator of peripheral inflammation. Brain-to-immune communication acts through cellular, humoral and neural pathways. In this context, the vagal nerve and the cholinergic anti-inflammatory pathway (CAP) have been shown to modify peripheral immune cell activity in both acute and chronic inflammatory conditions. However, the relevance of neuroimmune regulatory mechanisms following a surgical trauma is not yet elucidated. Twenty-five male patients undergoing elective laparoscopic abdominal surgery were included in this observational prospective study. Serial blood samples with extensive immune characterization, assessments of heart rate variability (HRV) and cognitive tests were performed before surgery and continuing up to 6 months post-surgery. Temporal immune responses revealed biphasic reaction patterns with most pronounced changes at 5 hours after skin incision and 14 days following surgery. Estimations of cardiac vagal nerve activity through HRV recordings revealed great individual variations depending on the pre-operative HRV baseline. A principal component analysis displayed distinct differences in systemic inflammatory biomarker trajectories primarily based on pre-operative HRV, with potiential consequences for long-term surgical outcomes. In conclusion, individual pre-operative HRV generates differential response patterns that associate with distinct inflammatory trajectories following surgery. Long-term surgical outcomes need to be examined further in larger studies with mixed gender cohorts.
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spelling pubmed-93016722022-07-22 The Neuroimmune Response to Surgery – An Exploratory Study of Trauma-Induced Changes in Innate Immunity and Heart Rate Variability Hildenborg, Malin Kåhlin, Jessica Granath, Fredrik Schening, Anna Granström, Anna Ebberyd, Anette Klevenvall, Lena Zetterberg, Henrik Han, Jinming Schlegel, Todd T. Harris, Robert Harris, Helena Erlandsson Eriksson, Lars I. Front Immunol Immunology Surgery triggers a systemic inflammatory response that ultimately impacts the brain and associates with long-term cognitive impairment. Adequate regulation of this immune surge is pivotal for a successful surgical recovery. We explored the temporal immune response in a surgical cohort and its associations with neuroimmune regulatory pathways and cognition, in keeping with the growing body of evidence pointing towards the brain as a regulator of peripheral inflammation. Brain-to-immune communication acts through cellular, humoral and neural pathways. In this context, the vagal nerve and the cholinergic anti-inflammatory pathway (CAP) have been shown to modify peripheral immune cell activity in both acute and chronic inflammatory conditions. However, the relevance of neuroimmune regulatory mechanisms following a surgical trauma is not yet elucidated. Twenty-five male patients undergoing elective laparoscopic abdominal surgery were included in this observational prospective study. Serial blood samples with extensive immune characterization, assessments of heart rate variability (HRV) and cognitive tests were performed before surgery and continuing up to 6 months post-surgery. Temporal immune responses revealed biphasic reaction patterns with most pronounced changes at 5 hours after skin incision and 14 days following surgery. Estimations of cardiac vagal nerve activity through HRV recordings revealed great individual variations depending on the pre-operative HRV baseline. A principal component analysis displayed distinct differences in systemic inflammatory biomarker trajectories primarily based on pre-operative HRV, with potiential consequences for long-term surgical outcomes. In conclusion, individual pre-operative HRV generates differential response patterns that associate with distinct inflammatory trajectories following surgery. Long-term surgical outcomes need to be examined further in larger studies with mixed gender cohorts. Frontiers Media S.A. 2022-07-07 /pmc/articles/PMC9301672/ /pubmed/35874666 http://dx.doi.org/10.3389/fimmu.2022.911744 Text en Copyright © 2022 Hildenborg, Kåhlin, Granath, Schening, Granström, Ebberyd, Klevenvall, Zetterberg, Han, Schlegel, Harris, Harris and Eriksson 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 Immunology
Hildenborg, Malin
Kåhlin, Jessica
Granath, Fredrik
Schening, Anna
Granström, Anna
Ebberyd, Anette
Klevenvall, Lena
Zetterberg, Henrik
Han, Jinming
Schlegel, Todd T.
Harris, Robert
Harris, Helena Erlandsson
Eriksson, Lars I.
The Neuroimmune Response to Surgery – An Exploratory Study of Trauma-Induced Changes in Innate Immunity and Heart Rate Variability
title The Neuroimmune Response to Surgery – An Exploratory Study of Trauma-Induced Changes in Innate Immunity and Heart Rate Variability
title_full The Neuroimmune Response to Surgery – An Exploratory Study of Trauma-Induced Changes in Innate Immunity and Heart Rate Variability
title_fullStr The Neuroimmune Response to Surgery – An Exploratory Study of Trauma-Induced Changes in Innate Immunity and Heart Rate Variability
title_full_unstemmed The Neuroimmune Response to Surgery – An Exploratory Study of Trauma-Induced Changes in Innate Immunity and Heart Rate Variability
title_short The Neuroimmune Response to Surgery – An Exploratory Study of Trauma-Induced Changes in Innate Immunity and Heart Rate Variability
title_sort neuroimmune response to surgery – an exploratory study of trauma-induced changes in innate immunity and heart rate variability
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9301672/
https://www.ncbi.nlm.nih.gov/pubmed/35874666
http://dx.doi.org/10.3389/fimmu.2022.911744
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