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Published on: August 7, 2017
Interleukin-18 binding protein in infants and children hospitalized with pneumonia in low-resource settings
Emily R Konrad1, Jeremy Soo1, Andrea L Conroy2
1Department of Pediatrics, University of Alberta, Edmonton, Canada.
Insights
Higher levels of Interleukin-18 binding protein (IL-18BP) in Ugandan children with pneumonia indicate increased disease severity and longer recovery times. This finding highlights IL-18BP as a potential biomarker for pediatric pneumonia outcomes.
Area of Science:
- Pediatric Infectious Diseases
- Immunology
- Biomarker Discovery
Background:
- Pneumonia is a leading infectious cause of child mortality, particularly in low- and middle-income countries.
- Interleukin-18 binding protein (IL-18BP), a natural antagonist of interleukin-18, is elevated in various inflammatory and infectious conditions.
Purpose of the Study:
- To investigate the association between admission IL-18BP levels and clinical severity in Ugandan children hospitalized with hypoxemic pneumonia.
- To explore the correlation of IL-18BP levels with indicators of disease severity and recovery time.
Main Methods:
- A prospective cohort study was conducted with 42 children admitted for hypoxemic pneumonia.
- IL-18BP levels were measured at admission and correlated with clinical signs of respiratory distress, the Pediatric Early Death Index for Africa (PEDIA-e) score, and time to clinical recovery milestones.
Main Results:
- Elevated IL-18BP levels were significantly associated with respiratory distress, including chest indrawing and nasal flaring (P < 0.05).
- IL-18BP levels showed a positive correlation with the composite clinical severity score (PEDIA-e, ρ = 0.46, P = 0.0020).
- Children with higher IL-18BP levels (>14 ng/mL) experienced significantly longer times to sit and to fever resolution (P < 0.05).
Conclusions:
- Higher admission IL-18BP levels in Ugandan children with pneumonia are linked to increased disease severity.
- IL-18BP may serve as a valuable biomarker for assessing pneumonia severity and predicting recovery duration in pediatric populations.
- Further research is warranted to explore the therapeutic implications of targeting the IL-18 pathway in severe pediatric pneumonia.
Abstract:
Pneumonia is the leading infectious cause of death in children, with especially high mortality in low- and middle-income countries. Interleukin-18 binding protein (IL-18BP) is a natural antagonist of the pro-inflammatory cytokine interleukin-18 and is elevated in numerous autoimmune conditions and infectious diseases. We conducted a prospective cohort study to determine the association between admission IL-18BP levels and clinical severity among children admitted to two hospitals in Uganda for hypoxemic pneumonia. A total of 42 children (median age of 1.2 years) were included. IL-18BP levels were higher in patients with respiratory distress, including chest indrawing (median 15 ng/mL (IQR 9.8-18) versus 4.5 ng/mL (IQR 3.8-11) without chest indrawing, P = 0.0064) and nasal flaring (median 15 ng/mL (IQR 9.7-19) versus 11 ng/mL (IQR 5.4-14) without nasal flaring, P = 0.034). IL-18BP levels were positively correlated with the composite clinical severity score, Pediatric Early Death Index for Africa (PEDIA-e, ρ = 0.46, P = 0.0020). Patients with IL-18BP > 14 ng/mL also had slower recovery times, including time to sit (median 0.69 days (IQR 0.25-1) versus 0.15 days (IQR 0.076-0.36) with IL-18BP < 14 ng/mL, P = 0.036) and time to fever resolution (median 0.63 days (IQR 0.16-2) versus 0.13 days (IQR 0-0.42), P = 0.016). In summary, higher IL-18BP levels were associated with increased disease severity and prolonged recovery times in Ugandan children with pneumonia.
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