Population-specific metabolic alterations in professional antigen-presenting cells contribute to sepsis-associated immunosuppression

Sepsis is a complex host response triggered by an infection, with the patient's immune system between hyper- and hypo-responsiveness being the main reason for the syndromes’ development and propagation. Studies conducted in peripheral blood mononuclear cells uncovered an association between an...

Full description

Saved in:
Bibliographic Details
Main Authors: Schenz, Judith (Author) , Uhle, Sandra (Author) , Nußhag, Christian (Author) , Brenner, Thorsten (Author) , Poschet, Gernot (Author) , Weigand, Markus A. (Author) , Uhle, Florian (Author)
Format: Article (Journal)
Language:English
Published: 2020
In: Shock
Year: 2020, Volume: 53, Issue: 1, Pages: 5-15
ISSN:1540-0514
DOI:10.1097/SHK.0000000000001337
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1097/SHK.0000000000001337
Verlag, lizenzpflichtig, Volltext: https://journals.lww.com/shockjournal/Abstract/2020/01000/Population_Specific_Metabolic_Alterations_in.2.aspx
Get full text
Author Notes:Judith Schenz, Sandra Tamulyte, Christian Nusshag, Thorsten Brenner, Gernot Poschet, Markus A. Weigand, Florian Uhle
Description
Summary:Sepsis is a complex host response triggered by an infection, with the patient's immune system between hyper- and hypo-responsiveness being the main reason for the syndromes’ development and propagation. Studies conducted in peripheral blood mononuclear cells uncovered an association between an impaired immunometabolism and the severity and outcome of the disease. With this prospective observational study, we aimed to evaluate the immunometabolic phenotype of monocytes and B cells and its association with the cell function. - Monocytes and B cells were isolated from patients with sepsis (n = 10; onset, days 4 and 8) and healthy volunteers (n = 10) and subsequently analyzed for metabolic changes and human leukocyte antigen-DR (HLA-DR) expression. Contemporaneously, immune checkpoints on monocytes and the ex vivo cytokine responses (interleukins 6 and 8) upon lipopolysaccharide or zymosan stimulation were analyzed. The distribution of B cell subsets was assessed, and plasma levels of immunoglobulins and tricarboxylic acid cycle intermediates were quantified. - Both monocytes and B cells exhibited decreased HLA-DR expression in patients with sepsis. Monocytes displayed a stable upregulated glycolysis while B cells augmented glycolysis and respiration over time. The monocytes’ ability to respond to stimulation was stimuli-dependently reduced but recovered over time. The B cell compartment shifted toward antibody-producing subsets and elevated immunoglobulins within the first days. - Our results provide evidence for the induction of a state of trained immunity in monocytes and an early but transient immunosuppressive phenotype accounting for peripheral sepsis-induced vulnerability to infections. B cells exhibit an unsustainable activation contributing to adaptive immunosuppression.
Item Description:Gesehen am 01.10.2020
Physical Description:Online Resource
ISSN:1540-0514
DOI:10.1097/SHK.0000000000001337