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Noninvasive Sampling of Mucosal Lining Fluid for the Quantification of In Vivo Upper Airway Immune-mediator Levels
Published on: August 7, 2017
Endotracheal colonization at birth is associated with a pathogen-dependent pro- and antiinflammatory cytokine
Jozef De Dooy1, Margareta Ieven, Wim Stevens
1Department of Pediatrics, Division of Neonatology, University of Antwerp, Faculty of Medicine, B-2610 Wilrijk. jd978722@planetinternet.be
Insights
Respiratory tract colonization in preterm infants triggers a dose-dependent cytokine and C-reactive protein (CRP) response. This inflammation is linked to both pathogens and commensal flora, highlighting infection risks in neonates.
Area of Science:
- Neonatal Medicine
- Microbiology
- Immunology
Background:
- Perinatal respiratory tract colonization in ventilated preterm infants is common.
- The relationship between respiratory colonization and inflammatory mediators like cytokines and C-reactive protein (CRP) is not fully understood.
Purpose of the Study:
- To investigate the association between endotracheal colonization and airway cytokine profiles.
- To examine the correlation between colonization and C-reactive protein (CRP) levels in umbilical cord blood.
Main Methods:
- Prospective cohort study of 141 ventilated preterm infants.
- Analysis of endotracheal aspirates for microbial colonization.
- Measurement of airway cytokines (IL-1β, IL-6, IL-8, TNF-α, IL-10, IL-12p70) and umbilical cord blood CRP.
Main Results:
- 26% of infants were colonized, with pathogens, commensals, and Mycoplasmataceae identified.
- Colonized infants showed increased pro-inflammatory (IL-1β, IL-6, IL-8, TNF-α) and anti-inflammatory (IL-10) cytokines in a dose-dependent manner.
- Gram-negative organism colonization elicited the strongest cytokine response. Commensal flora induced similar inflammatory responses as traditional pathogens. Umbilical cord blood CRP was elevated in colonized infants, particularly with Gram-negative organisms.
Conclusions:
- Endotracheal microorganisms in ventilated preterm infants induce a pathogen-specific, dose-dependent airway cytokine response.
- Systemic CRP levels are also associated with colonization, suggesting a link between respiratory microbes and neonatal inflammation.
Abstract:
The possible association between mediators of inflammation such as cytokines and perinatal colonization of the respiratory tract remains unclear. This prospective cohort study evaluated endotracheal colonization in 141 ventilated preterm infants at birth. The relation with cytokine response in the airways and C-reactive protein (CRP) in umbilical blood was investigated. Of the 141 preterm infants enrolled in this study, 37 (26%) were colonized. In addition to traditional pathogens (61%), commensal species (26%) and Mycoplasmataceae (13%) were isolated. Both the pro-inflammatory cytokines IL-1 beta, IL-6, IL-8, and tumor necrosis factor (TNF)-alpha as well as the antiinflammatory IL-10 are increased in colonized patients in a dose-dependent manner, with the strongest response in neonates colonized with Gram-negative organisms. There was no antimicrobial IL-12p70 response in colonized infants. Commensal flora is associated with the same inflammatory response as traditional pathogens. Although the umbilical cord blood CRP level was significantly higher in neonates with endotracheal colonization, it was highest in those colonized with Gram-negative organisms but still close to normal limits. Microorganisms in the endotracheal fluid of ventilated preterm infants are associated with a pathogen-specific and dose-dependent cytokine response in the airways and systemic CRP response.
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