Danger Signals Activating the Immune Response after Trauma

Sterile injury can cause a systemic inflammatory response syndrome (SIRS) that resembles the host response during sepsis. The inflammatory response following trauma comprises various systems of the human body which are cross-linked with each other within a highly complex network of inflammation. End...

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Main Authors: Stefanie Hirsiger, Hans-Peter Simmen, Clément M. L. Werner, Guido A. Wanner, Daniel Rittirsch
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2012/315941
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spelling doaj-3c14a042ec8b4c409562959f22d039ca2020-11-24T23:21:56ZengHindawi LimitedMediators of Inflammation0962-93511466-18612012-01-01201210.1155/2012/315941315941Danger Signals Activating the Immune Response after TraumaStefanie Hirsiger0Hans-Peter Simmen1Clément M. L. Werner2Guido A. Wanner3Daniel Rittirsch4Division of Trauma Surgery, Department of Surgery, University Hospital Zurich, 8091 Zurich, SwitzerlandDivision of Trauma Surgery, Department of Surgery, University Hospital Zurich, 8091 Zurich, SwitzerlandDivision of Trauma Surgery, Department of Surgery, University Hospital Zurich, 8091 Zurich, SwitzerlandDivision of Trauma Surgery, Department of Surgery, University Hospital Zurich, 8091 Zurich, SwitzerlandDivision of Trauma Surgery, Department of Surgery, University Hospital Zurich, 8091 Zurich, SwitzerlandSterile injury can cause a systemic inflammatory response syndrome (SIRS) that resembles the host response during sepsis. The inflammatory response following trauma comprises various systems of the human body which are cross-linked with each other within a highly complex network of inflammation. Endogenous danger signals (danger-associated molecular patterns; DAMPs; alarmins) as well as exogenous pathogen-associated molecular patterns (PAMPs) play a crucial role in the initiation of the immune response. With popularization of the “danger theory,” numerous DAMPs and PAMPs and their corresponding pathogen-recognition receptors have been identified. In this paper, we highlight the role of the DAMPs high-mobility group box protein 1 (HMGB1), interleukin-1α (IL-1α), and interleukin-33 (IL-33) as unique dual-function mediators as well as mitochondrial danger signals released upon cellular trauma and necrosis.http://dx.doi.org/10.1155/2012/315941
collection DOAJ
language English
format Article
sources DOAJ
author Stefanie Hirsiger
Hans-Peter Simmen
Clément M. L. Werner
Guido A. Wanner
Daniel Rittirsch
spellingShingle Stefanie Hirsiger
Hans-Peter Simmen
Clément M. L. Werner
Guido A. Wanner
Daniel Rittirsch
Danger Signals Activating the Immune Response after Trauma
Mediators of Inflammation
author_facet Stefanie Hirsiger
Hans-Peter Simmen
Clément M. L. Werner
Guido A. Wanner
Daniel Rittirsch
author_sort Stefanie Hirsiger
title Danger Signals Activating the Immune Response after Trauma
title_short Danger Signals Activating the Immune Response after Trauma
title_full Danger Signals Activating the Immune Response after Trauma
title_fullStr Danger Signals Activating the Immune Response after Trauma
title_full_unstemmed Danger Signals Activating the Immune Response after Trauma
title_sort danger signals activating the immune response after trauma
publisher Hindawi Limited
series Mediators of Inflammation
issn 0962-9351
1466-1861
publishDate 2012-01-01
description Sterile injury can cause a systemic inflammatory response syndrome (SIRS) that resembles the host response during sepsis. The inflammatory response following trauma comprises various systems of the human body which are cross-linked with each other within a highly complex network of inflammation. Endogenous danger signals (danger-associated molecular patterns; DAMPs; alarmins) as well as exogenous pathogen-associated molecular patterns (PAMPs) play a crucial role in the initiation of the immune response. With popularization of the “danger theory,” numerous DAMPs and PAMPs and their corresponding pathogen-recognition receptors have been identified. In this paper, we highlight the role of the DAMPs high-mobility group box protein 1 (HMGB1), interleukin-1α (IL-1α), and interleukin-33 (IL-33) as unique dual-function mediators as well as mitochondrial danger signals released upon cellular trauma and necrosis.
url http://dx.doi.org/10.1155/2012/315941
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