Septic Shock Clinical Trial
Official title:
Use of Fc Mannose-Binding Lectin to Detect and Monitor the Presence of Pathogen-Associated Molecular Patterns During Septic Shock
Use Mannose Binding Lectin (MBL) as a biomarker to measure levels of Pathogen- Associated Molecular Patterns (PAMP) during septic shock. This will allow evaluating interest of this biomarker to monitor and manage a septic shock. Consecutive patients admitted for sepsis in Intensive Care Unit Department will be included. This biomarker will be compared to all the parameters monitored usually for these patients in standard care.
Septic shock still represent a major cause of admission in intensive care unit, incidence of
severe sepsis is increasing, even in western countries, due to aging populations and
comorbidities. Definition of septic shock was revised in 2016 by a task force, which
emphasizes the need for future iterations. Indeed, there are no simple clinical or biological
criteria ton diagnose septic patients with high risk of shock, or to prognose its severity.
C-reactive protein (CRP) and procalcitonin (PCT) are the wider biomarkers used to monitor
septic patients. But they do not correlate with sepsis severity and moreover do not
distinguish unequivocally between infection and noninfected systemic inflammatory response
syndrome (SIRS). Each microorganism has number of PAMPs, cell wall components
(lipopolysaccharide endotoxin, peptidoglycan, outer membrane vesicles), flagella, mannan…
High levels of these pathogen fragments are released in the bloodstream during sepsis. They
trigger release of inflammatory cytokines that drive the sepsis cascade. Mannose binding
lectin plays a pivotal role in innate immunity, binding with surface sugars of wide range of
pathogens and their fragments. Thus MBL promotes opsonophagocytosis and activates the
lectin-complement pathway. Fc-MBL, an engineered version of MBL has been developed to capture
microorganism and treat sepsis. An ELISA, using Fc-MBL was developed to measure PAMPs in
whole blood during sepsis. This assay will use Fc-MBL ELISA to quantify PAMPs during septic
shock, to improve diagnostic and monitoring. But also, identifying patients with high levels
of PAMPs for dialysis-like sepsis therapies.
PAMP's level will be compared to clinical, biological, microbiological and therapeutic
outcomes. Its sensitivity will be evaluated by its kinetic among a septic shock (defined with
Sepsis-3 criteria) and by correlation with CRP (C-Reactive Protein) and PCT (Procalcitonin).
Its specificity will be evaluated by comparing its levels during septic and non-septic
shocks.
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