Gut dysbiosis in pediatric AR-FC comorbidity is associated with disruption of the microbiota-SCFA-immune axis, and while synbiotic therapy induced taxonomic shifts and improved gastrointestinal function, strain-specific formulations are needed for comprehensive immune and intestinal restoration.
Key Findings
Results
Children with allergic rhinitis-functional constipation comorbidity exhibited reduced gut microbial alpha-diversity compared to healthy controls.
Study enrolled 57 AR-FC children aged 0-6 years and 59 age-matched healthy controls (HC)
Alpha-diversity was significantly reduced in AR-FC subjects (P = 0.003)
Gut microbiota profiling was performed using 16S rRNA gene sequencing
Functional pathways were inferred via PICRUSt2
Results
SCFA-producing bacterial taxa were significantly depleted in AR-FC children compared to healthy controls.
Faecalibacterium prausnitzii was depleted with Log2FC = -2.1 (P = 0.001)
Bacteroides stercoris was depleted with Log2FC = -1.8 (P = 0.005)
These depletions suggest disruption of the microbiota-SCFA-immune axis
The depletions were associated with potential mucosal barrier defects and a bias toward Th2 polarization
Results
Altered functional metabolic pathways were observed in AR-FC children, including upregulated proteasome activity and suppressed LPS biosynthesis.
Proteasome activity was upregulated (P = 0.01), described as potentially linked to antigen processing
LPS biosynthesis was suppressed (P = 0.02), described as suggestive of impaired innate immunity
Functional pathway alterations were inferred using PICRUSt2 analysis
Results
Synbiotic intervention enriched Faecalibacterium abundance and alleviated constipation but reduced Bifidobacterium, reflecting substrate competition.
A subset of 13 preschoolers aged 3-7 years underwent a 3-month synbiotic intervention (multi-strain probiotics combined with dietary fiber)
Paired pre- and post-treatment samples were analyzed
Faecalibacterium abundance increased by +54.8% (P < 0.05)
Bifidobacterium abundance decreased by -85.2% (P < 0.05)
The decrease in Bifidobacterium was attributed to substrate competition
Results
Synbiotic intervention induced metabolic remodeling characterized by increased sulfur assimilation and diminished beta-lactam resistance.
Sulfate reduction increased by +83.2% (P = 0.04)
Beta-lactam resistance decreased by -35.4% (P = 0.03)
These changes were observed following the 3-month synbiotic intervention in 13 preschoolers
Discussion
Gut dysbiosis in AR-FC comorbidity was associated with disruption of the microbiota-SCFA-immune axis, potentially correlating with mucosal barrier defects and Th2 polarization bias.
Depletion of SCFA-producing taxa (F. prausnitzii and B. stercoris) was linked to immune-metabolic dysregulation
The authors proposed potential correlation with mucosal barrier defects
A potential bias toward T helper 2 (Th2) polarization was suggested as a consequence of the dysbiosis
The authors highlighted the need for strain-specific formulations to achieve comprehensive immune and intestinal restoration
Yang W, Zhang X, Wu B, Ni B, Lin H, Huang C. (2025). Gut microbiota-driven dysbiosis of the SCFA-immune axis in pediatric allergic rhinitis-constipation comorbidity: mechanisms and synbiotic remodeling.. Frontiers in immunology. https://doi.org/10.3389/fimmu.2025.1639359