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Stress molecules in sepsis and systemic inflammatory response syndrome
Authors:Adib-Conquy Minou  Cavaillon Jean-Marc
Institution:Unit Cytokines and Inflammation, Institut Pasteur, 28 rue Dr. Roux, 75015 Paris, France.
Abstract:During sepsis, microbial derived products ("pathogen-associated molecular patterns", PAMPs) are recognized as exogenous danger signals by specific sensors of the host ("pattern recognitions receptors", PRRs). This interaction leads to the release of numerous stress proteins that are a prerequisite to fight infection, though their overzealous production can contribute to tissue damage, organ dysfunction and eventually death. In critically ill patients, translocation of PAMPs can occur from the gut, and injured tissues and cells release endogenous danger signals called "alarmins" (e.g. High mobility group box-1); that share some properties with PAMPs. Thus, numerous similarities occur during infectious and non-infectious systemic inflammation.
Keywords:ARDS  acute respiratory distress syndrome  GM-CSF  granulocyte-macrophage colony stimulating factor  HMGB-1  High mobility group box-1  HSP  heat shock protein  HDL and LDL  High and low density lipoproteins  ICAM-1  intercellular adhesion molecule-1  ICU  intensive care unit  IFNγ  gamma-interferon  IL  interleukin  LBP  LPS binding protein  LPS  lipopolysaccharide  LTA  lipoteichoic acid  MOF  multiple organ failure  PAF  platelet-activating factor  PAMPs  pathogen-associated molecular patterns  PRRs  pattern recognitions receptors  SIRS  systemic inflammatory response syndrome  TLR  toll-like receptors  TNF  tumor necrosis factor  TREM-1  triggering receptor expressed on myeloid cells-1  VCAM-1  vascular cell adhesion molecule-1
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