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A Neonatal Imaging Model of Gram-Negative Bacterial Sepsis
Published on: August 12, 2020
Dendritic cells in childhood sepsis
Khalid I Elsayh1, Asmaa M Zahran, Ismail Lotfy Mohamad
1Pediatric Department, Faculty of Medicine, Assiut University, Assiut, Egypt.
Insights
Pediatric sepsis reduces dendritic cell (DC) levels and maturation. Lower DC numbers and maturation correlate with poorer sepsis prognosis, suggesting DCs as potential biomarkers.
Area of Science:
- Immunology
- Pediatric critical care
Background:
- Sepsis is a life-threatening organ dysfunction caused by a dysregulated host response to infection.
- Dendritic cells (DCs) are crucial immune regulators, orchestrating adaptive immunity.
Purpose of the Study:
- To investigate dendritic cell (DC) levels and maturation in pediatric sepsis patients.
- To determine the relationship between DC status and sepsis prognosis.
Main Methods:
- Flow cytometry was used to analyze DC subsets (plasmoid and monocytoid) and maturation markers (CD86, CD83).
- Evaluations were performed within 24 hours of ICU admission and at 28 days.
- Included 16 children with sepsis, 24 with complicated sepsis, and 40 healthy controls.
Main Results:
- Pediatric sepsis patients showed significantly lower DC levels and reduced CD86/CD83 expression compared to controls.
- Complicated sepsis cases exhibited more pronounced decreases in DC numbers and maturation markers.
- Higher baseline DC numbers and CD86/CD83 expression were observed in sepsis survivors.
Conclusions:
- Sepsis is associated with a diminished number and impaired maturation of dendritic cells.
- DC levels and maturation status may serve as valuable prognostic indicators for pediatric sepsis.
Purpose:
Our aim was to investigate the level and the maturation status of dendritic cells (DCs) in pediatric patients with sepsis and its relation to prognosis.
Materials And Methods:
The study included 16 children with sepsis, 24 children with complicated sepsis, and 40 healthy control children. The patients were investigated within 24 hours of intensive care unit admission and after 28 days. Flow cytometric detection of DCs was done.
Results:
Within 24 hours, the levels of both plasmoid DCs and monocytoid DCs and the expression of CD86 and CD83 on DCs were significantly lower in patients than in controls, and the difference was marked in patients with complicated sepsis. The amount of CD86 and CD83 per cell was significantly lower in patients with complicated sepsis. The baseline numbers of monocytoid DCs and plasmoid DCs were higher in the survival patients than in nonsurvival patients. In addition, the expression of CD86 and CD83 on the entire DCs was significantly higher in the survival patients with sepsis.
Conclusion:
Sepsis is associated with reduced level of DCs and decreases their maturation. The estimation of DCs number and maturation state may be used as prognostic makers of sepsis.
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