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Published on: April 13, 2010
Prospective assessment of protracted bacterial bronchitis: airway inflammation and innate immune activation
Julie M Marchant1,2, Peter G Gibson3, Terry V Grissell3
1Department of Respiratory Medicine, Royal Children's Hospital, Brisbane, Australia.
Insights
Protracted bacterial bronchitis (PBB) in children causes chronic moist cough. PBB involves significant airway neutrophilic inflammation and elevated inflammatory mediators, indicating innate immune activation.
Area of Science:
- Pediatric Pulmonology
- Infectious Diseases
- Immunology
Background:
- Protracted bacterial bronchitis (PBB) is a frequent cause of chronic moist cough in children.
- PBB is characterized by cough resolution with antibiotics and absence of alternative diagnoses.
- Understanding the airway inflammation in PBB is crucial for effective management.
Purpose of the Study:
- To detail the clinical presentation of PBB.
- To compare airway cellularity and inflammation promoters in children with PBB versus other chronic cough causes and controls.
- To investigate toll-like receptors (TLR)-2 and TLR-4 in PBB.
Main Methods:
- A cross-sectional study involving 100 children (PBB, other cough, controls) undergoing flexible bronchoscopy.
- Bronchoalveolar lavage (BAL) analysis included cytology, microbiology, IL-8, active MMP-9, and TLR-2/TLR-4 mRNA expression.
- Comparison of inflammatory markers between PBB patients and control groups.
Main Results:
- Children with PBB exhibited marked airway neutrophilia.
- Significantly elevated levels of IL-8 and active MMP-9 were observed in PBB patients compared to controls.
- Increased TLR-2 and TLR-4 mRNA expression was found in children with PBB.
Conclusions:
- PBB is characterized by intense neutrophilic airway inflammation.
- Elevated inflammatory mediators and innate immune activation are key features of PBB.
- These findings highlight the specific inflammatory profile of PBB in pediatric patients.
Abstract:
Protracted bacterial bronchitis (PBB) is a common cause of paediatric chronic moist cough. PBB is defined as the presence of isolated chronic moist cough which resolves with antibiotic therapy within 2 weeks and an absence of pointers suggesting alternative diagnoses. Our aim was to describe the clinical profile and examine the airway cellularity and likely promoters of neutrophilic inflammation in the bronchoalveolar lavage (BAL) of children with PBB compared with chronic cough due to other causes and controls. We explored the innate immune signaling receptors, toll-like receptors (TLR)-2 and TLR-4, as well as relevant effector molecules. A cross-sectional comparison was made of 100 children median age 2.58 years (with either PBB, coughing due to another cause or no cough controls) who underwent flexible bronchoscopy with lavage. BAL was evaluated for airway cytology, microbiology, inflammatory mediators interleukin 8 (IL-8) and active matrix metalloproteinase 9 (MMP-9) and TLR-2 and TLR-4 messenger RNA (mRNA) expression. Children with PBB had marked airway neutrophilia and increased median cytokine levels when compared to those with cough that resolved naturally and no cough controls: IL-8 0.67 versus 0.07 and 0.06 ng/ml (P < 0.005) and active MMP-9 7.25 versus 1.35 and 0.38 ng/ml (P < 0.005). The values for TLR-2 and TLR-4 mRNA expression were significantly elevated in children with PBB when compared to the control group. PBB is a paediatric condition which presents with chronic moist cough and its airway profile is characterized by intense neutrophilic airway inflammation with marked inflammatory mediator response and evidence of innate immune activation.
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