# Prebiotics and Synbiotics in Asthma: An Integrative Review of Human Trials and Murine Meta-Analysis

**Authors:** Louise C. Bonnard, Graham R. Sharpe, Matthew Martin, Georgina F. Dodd, Neil C. Williams

PMC · DOI: 10.3390/nu18040683 · Nutrients · 2026-02-20

## TL;DR

This study reviews how prebiotics and synbiotics may help manage asthma by reducing inflammation and improving lung function in both mice and humans.

## Contribution

The study provides an integrative review and meta-analysis of prebiotic and synbiotic effects on asthma in both human and murine trials.

## Key findings

- Prebiotics and synbiotics significantly reduced asthma-related inflammation and airway hyperresponsiveness in mice.
- Human trials showed improvements in lung function, asthma control, and reduced inflammation with prebiotic/synbiotic use.
- Synbiotics were effective in lowering type 2 cytokines and BALF cell counts in murine models.

## Abstract

Background/Objectives: The objectives of this study were to systematically review the literature on the effects of prebiotics and synbiotics on asthma control, lung function and asthma-associated inflammation from murine and human trials. Methods: A systematic review was performed following the PRISMA guidelines across multiple databases. A meta-analysis was performed on murine trials assessing asthma-associated inflammation and airway hyperresponsiveness, whilst a narrative review of human studies assessed asthma control, lung function, and inflammation. Results: Seventeen studies met the eligibility criteria for inclusion; eleven murine studies were included for meta-analysis and six human studies were for narrative review. The meta-analysis revealed significant effects of prebiotics and synbiotics on multiple markers of asthma-associated inflammation. Prebiotic intervention significantly reduced airway hyperresponsiveness (AHR) and type 2 cytokines (IL-4, IL-5, IL-13) and various cell counts, including neutrophil, macrophage, lymphocyte, eosinophil, and total bronchoalveolar (BALF). Synbiotics were also effective in reducing type 2 cytokines, including, IL-4, IL-5, IL-13, and lymphocytes, eosinophils, and total BALF cell count. A narrative review of human intervention trials of prebiotics and/or synbiotics revealed improvements in lung function, asthma control, and systemic and airway inflammation. Conclusions: This review indicates that dietary prebiotics and synbiotics may be suitable adjunct treatments to support asthma management, but further well-controlled human RCTs are required.

## Linked entities

- **Proteins:** IL4 (interleukin 4), IL5 (interleukin 5), IL13 (interleukin 13)
- **Diseases:** asthma (MONDO:0004979)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Fos (Fos proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 14281] {aka D12Rfj1, c-fos, cFos}, Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}, CCL17 (C-C motif chemokine ligand 17) [NCBI Gene 6361] {aka A-152E5.3, ABCD-2, SCYA17, TARC}, Ffar3 (free fatty acid receptor 3) [NCBI Gene 233080] {aka Gm478, Gpr41}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, Glb1 (galactosidase, beta 1) [NCBI Gene 12091] {aka Bge, Bgl, Bgl-e, Bgl-s, Bgl-t, Bgs}, Il1rl1 (interleukin 1 receptor-like 1) [NCBI Gene 17082] {aka DER4, Fit-1, Ly84, ST2L, St2, St2-rs1}, Cxcl15 (C-X-C motif chemokine ligand 15) [NCBI Gene 20309] {aka Il8, Scyb15, lungkine, weche}, Cd4 (CD4 antigen) [NCBI Gene 12504] {aka L3T4, Ly-4}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Ahr (aryl-hydrocarbon receptor) [NCBI Gene 11622] {aka Ah, Ahh, Ahre, In, bHLHe76}, IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, Ccl5 (C-C motif chemokine ligand 5) [NCBI Gene 20304] {aka MuRantes, RANTES, SISd, Scya5, TCP228}, Il5 (interleukin 5) [NCBI Gene 16191] {aka Il-5}, Zhx2 (zinc fingers and homeoboxes 2) [NCBI Gene 387609] {aka Afr-1, Afr1, Raf, mKIAA0854}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, Il4 (interleukin 4) [NCBI Gene 16189] {aka BSF-1, Il-4}, Il13 (interleukin 13) [NCBI Gene 16163] {aka Il-13}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Ffar2 (free fatty acid receptor 2) [NCBI Gene 233079] {aka GPCR43, Gpr43}, Serpinb1-ps1 (serine (or cysteine) peptidase inhibitor, clade B, member 1, pseudogene) [NCBI Gene 282665] {aka EID, ovalbumin}, Il33 (interleukin 33) [NCBI Gene 77125] {aka 9230117N10Rik, Il-33, Il1f11, NF-HEV}
- **Diseases:** HDM (MESH:D000092542), constipation (MESH:D003248), lung inflammation (MESH:D011014), allergic (MESH:D004342), atopic disease (MESH:D006969), diarrhoea (MESH:D003967), stomach-ache (MESH:D013272), vomiting (MESH:D014839), indigestion (MESH:D004415), deaths (MESH:D003643), inflammatory respiratory disease (MESH:D012140), AAI (MESH:D007249), headache (MESH:D006261), injury to (MESH:D014947), Hyperresponsiveness (MESH:D012130), GI symptoms (MESH:D012816), cough (MESH:D003371), airway eosinophilia (MESH:D004802), Asthma (MESH:D001249), dysbiosis (MESH:D064806)
- **Chemicals:** H2O (MESH:D014867), (poly)phenols (MESH:D059808), steroid (MESH:D013256), Prebiotics (MESH:D056692), luminal (MESH:D010634), nitric oxide (MESH:D009569), budesonide (MESH:D019819), SCFA (MESH:D005232), PBS (MESH:D007854), acetate (MESH:D000085), Inulin (MESH:D007444), maltodextrin (MESH:C008315), oligosaccharide (MESH:D009844), polyunsaturated fatty acids (MESH:D005231), Raffinose (MESH:D011887), M-16V (-), propionate (MESH:D011422), fructo-oligosaccharides (MESH:C116580), carbohydrate (MESH:D002241), Pectin (MESH:D010368), lactose (MESH:D007785), butyrate (MESH:D002087), glycans (MESH:D011134), nitrogen (MESH:D009584)
- **Species:** Pseudomonadota (proteobacteria, phylum) [taxon 1224], Cynara cardunculus var. scolymus (artichoke, varietas) [taxon 59895], Bifidobacterium animalis (species) [taxon 28025], Solanum tuberosum (potatoes, species) [taxon 4113], Lactobacillus acidophilus (species) [taxon 1579], gut metagenome (species) [taxon 749906], Lactiplantibacillus plantarum (species) [taxon 1590], Glycine max (soybean, species) [taxon 3847], Bifidobacterium longum subsp. infantis (subspecies) [taxon 1682], Lacticaseibacillus rhamnosus GG (strain) [taxon 568703], Lacticaseibacillus rhamnosus (species) [taxon 47715], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395]
- **Mutations:** M16V
- **Cell lines:** HMO — Homo sapiens (Human), Transformed cell line (CVCL_5G94)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12943301/full.md

## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943301/full.md

## References

60 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943301/full.md

---
Source: https://tomesphere.com/paper/PMC12943301