| Literature DB >> 30887636 |
Guillaume Monneret1,2, Morgane Gossez1,2, Nima Aghaeepour3, Brice Gaudilliere3, Fabienne Venet1,2.
Abstract
On May 2017, the World Health Organization (WHO) recognized sepsis as a global health priority by adopting a resolution to improve the prevention, diagnosis, and management of this deadly disease. While it has long been known that sepsis deeply perturbs immune homeostasis by inducing a tremendous systemic inflammatory response, pivotal observations based on clinical flow cytometry indicate that sepsis indeed initiates a more complex immune response that varies over time, with the concomitant occurrence of both pro- and anti-inflammatory mechanisms. As a resultant, some septic patients enter a stage of protracted immunosuppression. This paved the way for immunostimulation approaches in sepsis. Clinical flow cytometry permitted this evolution by drawing a new picture of pathophysiology and reshaping immune trajectories in patients. Additional information from cytometry by time of flight mass cytometry and other high-dimensional flow cytometry platform should rapidly enrich our understanding of this complex disease. This review reports on landmarks of clinical flow cytometry in sepsis and how this single-cell analysis technique permitted to breach the wall of decades of unfruitful anti-inflammatory-based clinical trials in sepsis.Entities:
Keywords: HLA-DR; IL-7; PD-1; flow cytometry; monocyte; sepsis; time of flight mass spectrometry
Year: 2019 PMID: 30887636 PMCID: PMC6461502 DOI: 10.1002/cyto.a.23749
Source DB: PubMed Journal: Cytometry A ISSN: 1552-4922 Impact factor: 4.355