Community Series in Translational Insights into Mechanisms and Therapy of Organ Dysfunction in Sepsis and Trauma, volume III

52.6K

views

49

authors

20

articles

Community Series in Translational Insights into Mechanisms and Therapy of Organ Dysfunction in Sepsis and Trauma, volume III

52.6K

views

49

authors

20

articles

Editorial

11 July 2024

Editorial: Community series in translational insights into mechanisms and therapy of organ dysfunction in sepsis and trauma - volume III

Borna Relja

,

Pietro Ghezzi

,

Sina M. Coldewey

,

Valentin A. Pavlov

, 2 more and

Christoph Thiemermann

743 views

0 citations

Editors

0

Impact

Fetching...

About

Life-threatening organ dysfunction/failure in critically ill patients suffering from sepsis or trauma is caused by a dysregulated host response to infection and/or inflammation. Despite significant advances in our understanding of some of the key signaling pathways involved in the excessive inflammation associated with sepsis/trauma, the translation of our current understanding of the underlying pathophysiology into organ-protective therapeutic strategies is still very limited. Current therapeutic approaches, hence, continue to rely on source control, antibiotics and supportive care, and particularly early goal-directed therapy.The organ dysfunction/failure associated with trauma and/or sepsis is associated with excessive systemic inflammation, secondary to extensive tissue damage and ischemia reperfusion injury. The endothelial glycocalyx is one of the earliest sites involved in triggering the potentially overwhelming pro-inflammatory response induced. Alterations to its structure affect (i) endothelial permeability and (ii) the secretion and activation of sheddases, leading to the release of degradation products of the endothelial glycocalyx (endogenous damage/danger associated molecular patterns; DAMPs). In addition to pathogen-associated molecular patterns (PAMPs) released from pathogens, DAMPs trigger and amplify the systemic inflammation present in patients suffering from many forms of critical illness. Thus, the injury of the glycocalyx and the consecutive release of DAMPs jointly contribute to and drive a potentially excessive, local and systemic inflammation which lead to organ injury/dysfunction including acute kidney injury, respiratory failure and cardiomyopathy, to name but a few.In this Research Topic, we aim to shed new light on the molecular mechanisms involved in inflammation in critical illness with a focus on preclinical and translational studies targeting new organ-protective, therapeutic strategies in sepsis and trauma.This Research Topic is the third volume of the “Community Series in Translational Insights into Mechanisms and Therapy of Organ Dysfunction in Sepsis and Trauma”. Please see the first volume here, and the second volume here"

Life-threatening organ dysfunction/failure in critically ill patients suffering from sepsis or trauma is caused by a dysregulated host response to infection and/or inflammation. Despite significant advances in our understanding of some of the key signaling pathways involved in the excessive inflammation associated with sepsis/trauma, the translation of our current understanding of the underlying pathophysiology into organ-protective therapeutic strategies is still very limited. Current therapeutic approaches, hence, continue to rely on source control, antibiotics and supportive care, and particularly early goal-directed therapy.The organ dysfunction/failure associated with trauma and/or sepsis is associated with excessive systemic inflammation, secondary to extensive tissue damage and ischemia reperfusion injury. The endothelial glycocalyx is one of the earliest sites involved in triggering the potentially overwhelming pro-inflammatory response induced. Alterations to its structure affect (i) endothelial permeability and (ii) the secretion and activation of sheddases, leading to the release of degradation products of the endothelial glycocalyx (endogenous damage/danger associated molecular patterns; DAMPs). In addition to pathogen-associated molecular patterns (PAMPs) released from pathogens, DAMPs trigger and amplify the systemic inflammation present in patients suffering from many forms of critical illness. Thus, the injury of the glycocalyx and the consecutive release of DAMPs jointly contribute to and drive a potentially excessive, local and systemic inflammation which lead to organ injury/dysfunction including acute kidney injury, respiratory failure and cardiomyopathy, to name but a few.In this Research Topic, we aim to shed new light on the molecular mechanisms involved in inflammation in critical illness with a focus on preclinical and translational studies targeting new organ-protective, therapeutic strategies in sepsis and trauma.This Research Topic is the third volume of the “Community Series in Translational Insights into Mechanisms and Therapy of Organ Dysfunction in Sepsis and Trauma”. Please see the first volume here, and the second volume here"

Download ebook

Share

Editors

Impact

52,628 Total views

31,970 Article views

18,996 Article downloads

1,662 Topic views

Published In

Journal Thumbnail

Frontiers in Immunology

About Frontiers Research Topics

With their unique mixes of varied contributions from Original Research to Review Articles, Research Topics unify the most influential researchers, the latest key findings and historical advances in a hot research area! Find out more on how to host your own Frontiers Research Topic or contribute to one as an author.

Suggest a topic