Related Experiment Video
Updated: Aug 7, 2026

Visualizing Lung Cellular Adaptations during Combined Ozone and LPS Induced Murine Acute Lung Injury
Published on: March 21, 2021
Age-related leukocyte and cytokine patterns in community-acquired bronchopneumonia
Ami Ballin1, Alla Osadchy, Alla Osdachi
1Department of Pediatrics, Wolfson Medical Center, Holon, Israel. ballin@wolfson.health.gov.il
Insights
Community-acquired bronchopneumonia shows higher leukocyte counts in children than adults. Inflammatory cytokine levels were similar, but immune responses appear age-dependent.
Area of Science:
- Pediatric and adult infectious diseases
- Immunology
- Hematology
Background:
- Community-acquired bronchopneumonia (CABP) often presents with extreme leukocytosis in children, unlike adults.
- Limited data exists on serum inflammatory cytokine differences between pediatric and adult CABP patients.
Purpose of the Study:
- To compare leukocyte counts and serum inflammatory cytokine levels in pediatric and adult patients diagnosed with CABP.
Main Methods:
- Prospective evaluation of pediatric and adult patients admitted for CABP based on clinical and chest X-ray findings.
- Analysis of complete blood counts and serum concentrations of granulocyte colony-stimulating factor (G-CSF), interleukins (IL-6, IL-8, IL-10), interferon-gamma, tumor necrosis factor, matrix metalloproteinase-9 (MMP-9), and intercellular adhesion molecule-1.
Main Results:
- Mean leukocyte counts were significantly higher in children (21,018/mm3) than adults (12,628/mm3).
- Age was inversely correlated with leukocyte and platelet counts in the pediatric group.
- While overall cytokine levels did not differ significantly, age correlated positively with MMP-9, IL-8, and G-CSF.
Conclusions:
- The immune response in community-acquired bronchopneumonia exhibits age-dependent characteristics.
- Leukocyte count differences in CABP between children and adults may be influenced by age-related immune responses.
Background:
Community-acquired bronchopneumonia in children is frequently accompanied by extreme leukocytosis, whereas in adults with the same diagnosis a high leukocyte count is uncommon. Data regarding differences in the serum levels of inflammatory cytokines between children and adults are limited.
Objectives:
To compare leukocyte counts and blood levels of various inflammatory cytokines in children and adults diagnosed with community-acquired bronchopneumonia.
Methods:
We prospectively evaluated all pediatric and adult patients admitted for bronchopneumonia based on clinical and chest X-ray findings. Blood was drawn for complete blood count and serum concentration of the following cytokines: granulocyte colony-stimulating factor, interleukins-6, 8 and 10, interferon-gamma, tumor necrosis factor, as well as matrix metalloproteinase-9 and intercellular adhesion molecule-1.
Results:
There were 31 children and 32 adults. The patients in both groups had similar parameters of infection severity. None of them required admission to the Intensive Care Unit. Mean (+/- SD) leukocyte counts in the pediatric and adult groups were 21,018/mm3 (+/- 10,420) and 12,628/mm3 (+/- 6735) respectively (P = 0.02). Age was inversely correlated with leukocytes in the pediatric group (P = 0.0001). A significant inverse correlation was also found between age and platelet counts. Although cytokine levels in both groups were not significantly different, age was directly correlated with MMP-9 (P= 0.03), IL-8 (P= 0.03) and G-CSF (P= 0.014).
Conclusions:
The immune response in community-acquired bronchopneumonia is, at least partly, age-dependent.
Related Concept Videos
Atypical Pneumonia
Chronic Obstructive Pulmonary Disease III: Chronic Bronchitis Features
Pneumonia I: Introduction
Pneumonia I: Introduction
Risk Factors
Various factors influence the likelihood of developing pneumonia. Age plays a crucial role, with infants, children under two, and individuals over 65 at increased risk due to their...
Pneumonia II: Pathophysiology
Chronic Obstructive Pulmonary Disease-II: Pathophysiology
Chronic Inflammation

