# Probiotic supplementation modulates the gut microbiome and improves clinical outcomes in pediatric refractory asthma

**Authors:** Zheng Liu, Wen Deng, Wenlin Xu, Linlin Ye, Zhihui Rao

PMC · DOI: 10.3389/fmicb.2026.1756436 · Frontiers in Microbiology · 2026-02-11

## TL;DR

Adding probiotics to standard treatment improves asthma control and gut health in children with severe asthma.

## Contribution

Demonstrates that multi-strain probiotics improve asthma outcomes and restore gut microbiome balance in children.

## Key findings

- Combination therapy achieved complete asthma control in 68.18% of patients versus 36.36% with conventional therapy.
- Probiotic treatment increased alpha diversity and elevated Bifidobacterium while reducing Bacteroides.

## Abstract

Refractory asthma in children remains a clinical challenge despite conventional therapies, with emerging evidence linking gut microbiome dysbiosis to persistent inflammation via the gut-lung axis. This study investigated whether multi-strain probiotic supplementation could improve asthma control and restore microbial balance when added to standard treatment.

This prospective randomized controlled trial enrolled 88 children aged 4–8 years with refractory asthma. Participants were allocated into two groups (n = 44 each): a conventional treatment group (bronchodilators and glucocorticoids) and a combination treatment group, which received conventional therapy plus a multi-strain probiotic (Bifidobacterium, Lactobacillus acidophilus, Streptococcus thermophilus) for 4 months. Primary outcomes were asthma control level, Asthma Control Test (ACT) scores, and pulmonary function (FEV₁, FVC, PEF). Secondary outcomes included gut microbiota changes, assessed by 16S rRNA gene sequencing.

Combination therapy achieved complete asthma control in 68.18% of patients versus 36.36% with conventional therapy (Z = 2.415, p < 0.05). Post-treatment ACT scores were higher in the combination group (22.45 ± 1.20 vs. 19.78 ± 1.45; p < 0.05), with superior improvements in FEV1 (2.65 ± 0.10 L vs. 2.30 ± 0.08 L; p < 0.001), FVC (3.10 ± 0.18 L vs. 2.80 ± 0.15 L; p < 0.001), and PEF (4.00 ± 0.25 L/s vs. 3.50 ± 0.20 L/s; p < 0.001). Symptoms resolved faster with combination therapy (e.g., cough: 5.60 ± 1.50 vs. 10.45 ± 2.30 days; p < 0.05). Microbiome analysis showed increased alpha diversity (e.g., Shannon index: p < 0.05) and beneficial shifts in the combination group, including higher Bifidobacterium (25.00 ± 15.31% vs. 0.98 ± 1.92%; p < 0.001) and reduced Bacteroides, with distinct beta diversity clustering (PERMANOVA p < 0.05).

Adjunctive multi-strain probiotics enhance clinical outcomes and gut microbiome health in pediatric refractory asthma, supporting microbiome-targeted therapies via the gut-lung axis. Larger, double-blind randomized controlled trials are warranted to confirm long-term benefits.

## Linked entities

- **Diseases:** asthma (MONDO:0004979)

## Full-text entities

- **Genes:** PKD1 (polycystin 1, transient receptor potential channel interacting) [NCBI Gene 5310] {aka PBP, PC1, Pc-1, TRPP1, eliosin}
- **Diseases:** eczema (MESH:D004485), respiratory disease (MESH:D012140), congenital respiratory tract malformations (MESH:D012141), inflammation (MESH:D007249), cough (MESH:D003371), Asthma (MESH:D001249), congenital heart disease (MESH:D006330), digestive system diseases (MESH:D004066), Dyspnea (MESH:D004417), dysbiosis (MESH:D064806), gastrointestinal infection (MESH:D005767), diarrhea (MESH:D003967), lung inflammation (MESH:D011014), allergic conditions (MESH:D004342), respiratory disorders (MESH:D012131), rhinitis (MESH:D012220), wheezing (MESH:D012135), chronic (MESH:D002908), vomiting (MESH:D014839), primary immunodeficiency diseases (MESH:D000081207)
- **Chemicals:** salbutamol (MESH:D000420), Sodium Phosphate (MESH:C018279), PPS (-), butyrate (MESH:D002087), agarose (MESH:D012685), mepolizumab (MESH:C434107), water (MESH:D014867), guanidine isothiocyanate (MESH:C054435), budesonide (MESH:D019819), SCFA (MESH:D005232)
- **Species:** Faecalibacterium (genus) [taxon 216851], Clostridium (genus) [taxon 1485], Bifidobacterium (genus) [taxon 1678], Homo sapiens (human, species) [taxon 9606], Prevotella (genus) [taxon 838], Bacteroides (genus) [taxon 816], Fusobacterium (genus) [taxon 848], Lactobacillus acidophilus La-14 (strain) [taxon 1314884], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Lactobacillus acidophilus (species) [taxon 1579], gut metagenome (species) [taxon 749906], Streptococcus thermophilus (species) [taxon 1308]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12932546/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932546/full.md

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Source: https://tomesphere.com/paper/PMC12932546