Bronchiectasis in children: a systematic review of cytokine profile, immune cell phenotypes and microbiota in bronchoalveolar lavage fluid

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Authors: Christian Magnus Kragh Thomsen, Simon Kromann-Thomsen, Signe Bødker Thim, Sune Rubak
Cited by: 1
References: 82

Abstract

BACKGROUND: Paediatric noncystic fibrosis bronchiectasis (NCFB) is a chronic respiratory condition characterised by airway infection, chronic inflammation, mucociliary dysfunction and structural lung damage. Emerging evidence highlights the importance of the local immune response and microbial environment in driving disease progression. OBJECTIVES: This systematic review aimed to summarise contemporary evidence on bronchoalveolar lavage (BAL)-derived cytokine levels, immune cell phenotypes and microbiota in paediatric NCFB, with a focus on their role in disease pathogenesis, phenotype classification and potential to inform targeted interventions. METHODS: The review followed PRISMA guidelines and was registered with PROSPERO (CRD42024520391). Six electronic databases were searched for studies investigating BAL cytokines, immune cells or microbiota in paediatric NCFB. Data extraction followed a pre-defined template and methodological quality was assessed using the RoB 2.0 and AXIS tools. RESULTS: and BAL-derived immunological biomarkers. Cytokine profiling demonstrated consistent elevations of pro-inflammatory mediators, notably interleukin-8, with variable associations to disease severity and pathogen-specific immune responses. Microbiota analyses, though limited, suggest that paediatric NCFB is not defined by a distinct microbial signature of the lower airways. CONCLUSION: Current evidence supports a model in which neutrophilic inflammation, driven by dysregulated cytokine responses and potentially sustained by microbial dysbiosis, is central to the pathophysiology of paediatric NCFB. Key gaps remain regarding dysbiosis, adaptive immunity and the longitudinal trajectories of immune mediators. Addressing these may support biomarker development and targeted therapies.

Fields of Study & Subjects

Cystic Fibrosis Research Advances Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis Chronic Obstructive Pulmonary Disease (COPD) Research

Publication details

Journal / source
European Respiratory Review
Publisher
European Respiratory Society (ERS)
Volume
35
Issue
179
Pages
250071–250071
Publication date
1 January 2026
Language
EN