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Updated: Feb 12, 2026

Characterization of Human Monocyte Subsets by Whole Blood Flow Cytometry Analysis
Published on: October 17, 2018
HLA-DR Expression on Monocyte Subsets in Critically Ill Children
Navin P Boeddha1,2, Dorian Kerklaan1, Albert Dunbar2
1From the Intensive Care and Department of Pediatric Surgery.
Insights
In critically ill children, monocytic human leukocyte antigen-DR (HLA-DR) expression declines, particularly in sepsis patients. Low HLA-DR on classical monocytes indicates increased risk of nosocomial infections and mortality.
Area of Science:
- Immunology
- Pediatric Critical Care
Background:
- Sepsis, surgery, and trauma impact children's immune responses.
- Monocyte subsets and human leukocyte antigen-DR (HLA-DR) expression are key immune indicators.
Purpose of the Study:
- To longitudinally assess blood monocyte subset distribution and HLA-DR expression in critically ill children.
- To correlate these immune markers with outcomes like nosocomial infections and mortality.
Main Methods:
- Flow cytometry was used to analyze monocyte subsets and HLA-DR expression.
- Measurements were taken upon admission and on days 2, 3, and 4 in the pediatric intensive care unit (PICU).
- Comparison was made between critically ill children and healthy controls.
Main Results:
- Critically ill children showed a higher proportion of classical monocytes (CD14++CD16-) upon PICU admission compared to controls.
- HLA-DR expression was significantly decreased in all monocyte subsets, most notably on classical monocytes and in sepsis patients.
- Lower HLA-DR expression on classical monocytes at days 2 and 3 was associated with subsequent nosocomial infections and mortality.
Conclusions:
- Monocytic HLA-DR expression decreases during PICU stay, especially in sepsis.
- Reduced HLA-DR on classical monocytes serves as a potential biomarker for adverse outcomes in critically ill children.
Background:
To longitudinally study blood monocyte subset distribution and human leukocyte antigen-DR (HLA-DR) expression on monocyte subsets in children with sepsis, post-surgery and trauma in relation to nosocomial infections and mortality.
Methods:
In 37 healthy children and 37 critically ill children (12 sepsis, 11 post-surgery, 10 trauma and 4 admitted for other reasons)-participating in a randomized controlled trial on early versus late initiation of parenteral nutrition-monocyte subset distribution and HLA-DR expression on monocyte subsets were measured by flow cytometry upon admission and on days 2, 3 and 4 of pediatric intensive care unit (PICU) stay.
Results:
Upon PICU admission, critically ill children had a higher proportion of classical monocytes (CD14++CD16-) than healthy children [PICU 95% (interquartile range [IQR] 88%-98%); controls, 87% (IQR 85%-90%), P < 0.001]. HLA-DR expression was significantly decreased within all monocyte subsets and at all time points, being most manifest on classical monocytes and in patients with sepsis. Percentage of HLA-DR expressing classical monocytes [upon PICU admission 67% (IQR 44%-88%); controls 95% (IQR 92%-98%), P < 0.001], as well as the HLA-DR mean fluorescence intensity [upon PICU admission 3219 (IQR 2650-4211); controls 6545 (IQR 5558-7647), P < 0.001], decreased during PICU stay. Patients who developed nosocomial infections (n = 13) or who died (n = 6) had lower HLA-DR expression on classical monocytes at day 2 (P = 0.002) and day 3 (P = 0.04), respectively.
Conclusions:
Monocytic HLA-DR expression decreased during PICU stay and was lower compared with controls on all examined time points, especially on classical monocytes and in children admitted for sepsis. Low HLA-DR expression on classical monocytes was associated with nosocomial infections and death.
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