HHE Sponsored supplement: Sepsis | Page 11

pathophysiology Pathophysiology of sepsis The pathophysiology of sepsis is extremely complex and mechanisms of multiple organ system dysfunction and immune system alterations are reviewed here Francisco Valenzuela Sánchez Department of Critical Care Medicine, University Hospital SAS of Jerez, Jerez de la Frontera, Cadiz, Spain Blanca Valenzuela Méndez Gynecology and Obstetrics Departament, Universitary Hospital Germans Trias i Pujol; Department of Medicine, Universitat Autónoma de Barcelona, Barcelona, Spain Juan Francisco Rodríguez Gutiérrez Hematology Department, University Hospital SAS of Jerez, Jerez de la Frontera, Cadiz, Spain Jordi Rello MD PhD CIBERES, Barcelona. Vall d´Hebron Institut of Research (VHIR), Universitat Autónoma de Barcelona, Barcelona, Spain Sepsis is an uncontrolled inflammatory response induced by infection. 1 The innate immune system is the first line of defence against an infectious insult, which conditions the adaptive response with the objective of neutralising the aggressor(s). At the same time, a compensatory anti-inflammatory response and the process of repairing tissue damage is generated. 2 If this inflammatory response goes beyond the local level, it becomes a systemic reaction, with potentially catastrophic results. Added to this are the characteristics of the micro-organisms and of the host, which also affect the manifestation of sepsis. 3 Due to mechanisms that have not been fully clarified, a series of cellular alterations occur that lead to organ failure and that constitute the basis of the organ dysfunction, the basis of the current concept of sepsis in the Sepsis-3 consensus conference. 4 Alteration of the immune function in sepsis Innate immunity The innate immune system is the first line of defence against pathogens and comprises physical and chemical barriers, cells and circulating effector proteins. In inflammatory activation, damage-associated molecular patterns (DAMPs), of both micro-organisms (PAMPs) and endogenous products from damaged tissues (alarmines), are recognised through host molecules called pattern recognition receptors (Figure 1), the most notable members of which are the Toll-like receptors (TLR). 1–3 The binding of a TLR to a specific ligand results in activation of a series of adaptor proteins present in the cell cytoplasm (Table 1). 5–7 Activation of NK-κB Following this, nuclear factor kappa-light-chain- enhancer of activated B cells (NF-κB) binds to various promoters to activate the transcription figure 1 Sequence of inflammatory activation due to bacterial infection and its evolution into acute organ injury Neutrophil chemotaxis Host cell Apoptosis DAMPs N-formyl peptides Mitochondrial DNA FPR1 TLR9 p38 MAPK Neutrophil PAMPs Bacterial DNA N-formyl peptides Acute injury TLR9 FPR1 Bacteria Neutrophil chemotaxis 11 HHE 2018 | hospitalhealthcare.com