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Absorption of Nasal and Bronchial Fluids: Precision Sampling of the Human Respiratory Mucosa and Laboratory Processing of Samples
Published on: January 21, 2018
Increased eosinophilic cationic protein in nasal fluid in hospitalized wheezy infants with RSV infection
Naoko Okamoto1, Masanori Ikeda, Masato Okuda
1Department of Pediatrics, National Hospital Organization, Fukuyama Medical Center, Hiroshima, Japan.
Insights
Nasal fluid eosinophilic cationic protein (ECP) is elevated in infants hospitalized with respiratory syncytial virus (RSV) and wheezing. This suggests ECP may indicate airway inflammation in young children with RSV infection.
Area of Science:
- Pediatrics
- Immunology
- Respiratory Medicine
Background:
- Respiratory syncytial virus (RSV) causes bronchiolitis in infants, potentially leading to asthma.
- The link between RSV bronchiolitis and later allergic sensitization needs further pathophysiological characterization.
Purpose of the Study:
- To evaluate airway inflammation in RSV bronchiolitis by comparing eosinophilic cationic protein (ECP) levels.
- To analyze ECP concentrations in nasal fluid and plasma of infants hospitalized with lower respiratory tract infections.
Main Methods:
- Collected nasal fluid and plasma from 69 infants (<2 years) hospitalized with lower respiratory tract infections.
- Measured eosinophilic cationic protein (ECP) concentrations in nasal fluid and plasma samples.
Main Results:
- Nasal fluid ECP levels were significantly higher in infants with wheezing and in those infected with RSV.
- Plasma ECP levels showed no significant difference based on wheezing or RSV infection status.
- Nasal fluid ECP concentrations correlated with peripheral blood neutrophil and eosinophil counts.
Conclusions:
- Elevated nasal fluid ECP indicates leukocyte-mediated airway inflammation in infants with RSV infection and wheezing.
- ECP in nasal fluid may originate from both neutrophils and eosinophils in the airways.
- Monitoring nasal fluid ECP can help assess leukocyte-mediated airway inflammation severity in infants.
Background:
Respiratory syncytial virus (RSV) is a major respiratory pathogen which causes bronchiolitis with dyspnea and wheezing in children less than 2 years old. RSV bronchiolitis in infancy severe enough to cause hospitalization might be a risk factor for allergic sensitization and bronchial asthma in future. However, the pathophysiology behind this development has not been clearly characterized. To evaluate the existence of airway inflammation and characteristic of RSV bronchiolitis, we analyzed and compared the concentrations of eosinophilic cationic protein (ECP) in nasal fluid and plasma.
Methods:
From 69 infants (aged <2 years) hospitalized for possible lower respiratory tract infections including RSV infection, we collected nasal fluid and plasma and determined the ECP concentrations.
Results:
ECP concentrations in nasal fluid were significantly higher in patients with wheezing and/or bronchial rales than in patients without them (1733 ± 660 ng/mL vs 680 ± 450 ng/mL, p = 0.018), and those of the respiratory syncitial virus-infected group were significantly higher than those of the uninfected group (p = 0.04). Meanwhile, there was no significant difference in plasma ECP levels between patients with wheezing and patients without wheezing, and no significant difference between RSV-infected and other pathogen-infected patients. There were significant correlations between nasal fluid ECP concentrations and both neutrophil and eosinophil counts in the peripheral blood.
Conclusions:
Nasal fluid ECP concentrations are increased in infants with lower respiratory infections including RSV infection accompanied with wheezing. ECP probably originates from neutrophils as well as eosinophils migrated into airways. The monitoring of ECP concentration in nasal fluid may be useful for evaluating leukocyte (including eosinophils and neutrophils)-mediated airway inflammation during infancy and its severity.
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