# Possible Crosstalk Between Small Intestinal Bacterial Overgrowth (SIBO) and Atopic Manifestations—A Short Overview

**Authors:** Michał Terlecki, Wiktoria Brzeczek, Martyna Kowalczyk, Emilia Kiełczyńska, Klaudia Kukla, Gabriela Osmulska, Krzysztof Gomułka

PMC · DOI: 10.3390/ijms27041865 · International Journal of Molecular Sciences · 2026-02-15

## TL;DR

This paper explores the possible link between small intestinal bacterial overgrowth (SIBO) and atopic conditions like asthma and allergies, suggesting SIBO may worsen symptoms through immune system changes.

## Contribution

The paper introduces the concept of a 'gut–allergy axis' and highlights SIBO's potential role in triggering allergic immune responses.

## Key findings

- SIBO prevalence is highest in bronchial asthma and food allergy patients.
- Treating SIBO improved symptoms in bronchial asthma and mast cell activation syndrome.
- SIBO may trigger Th2 immune responses and increase allergic interleukins like IL-4, IL-5, and IL-13.

## Abstract

Small intestinal bacterial overgrowth (SIBO) is an increasingly recognized condition that influences immune responses. It may be linked to atopic disorders such as bronchial asthma (BA), food allergies (FA), chronic spontaneous urticaria (CSU), and mast cell activation syndrome (MCAS). The aim of our study was to perform a structured literature search to assess the possible correlation between SIBO and the presentation of atopic disorders. The prevalence of SIBO was highest in patients with BA (60–100%) and FA (50–87.5%), followed by MCAS (30.9%) and CSU (27.9%). The diagnosis of SIBO was based on lactulose or glucose breath tests. SIBO exacerbated symptoms of atopic diseases, and treating it within BA and MCAS improved the symptoms, in contrast to CSU. The present evidence suggests a possible crosslink between SIBO and atopic manifestations. Bacterial overgrowth appears to trigger the Th2 immune response via the mucosal pathway and low-grade endotoxemia. These result in the increased synthesis of interleukins involved in allergic reactions (IL-4, IL-5, IL-13). Further studies are essential to confirm the clinical significance of this association. The “gut–allergy axis” may offer new therapeutic options and possibly improve quality of life in patients with atopy.

## Linked entities

- **Diseases:** mast cell activation syndrome (MONDO:0100004)

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, IL17RB (interleukin 17 receptor B) [NCBI Gene 55540] {aka CRL4, EVI27, IL17BR, IL17RH1}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, GATA3 (GATA binding protein 3) [NCBI Gene 2625] {aka HDR, HDRS}, FCER1A (Fc epsilon receptor Ia) [NCBI Gene 2205] {aka FCE1A, FCERIA, FcERI}, IL25 (interleukin 25) [NCBI Gene 64806] {aka IL17E}, CCL11 (C-C motif chemokine ligand 11) [NCBI Gene 6356] {aka SCYA11}, C3 (complement C3) [NCBI Gene 718] {aka AHUS5, ARMD9, ASP, C3a, C3b, CPAMD1}, CCL26 (C-C motif chemokine ligand 26) [NCBI Gene 10344] {aka IMAC, MIP-4a, MIP-4alpha, SCYA26, TSC-1}, IL9 (interleukin 9) [NCBI Gene 3578] {aka HP40, IL-9, P40}, ITGAM (integrin subunit alpha M) [NCBI Gene 3684] {aka CD11B, CR3A, HNA-4, MAC-1, MAC1A, MO1A}, IL33 (interleukin 33) [NCBI Gene 90865] {aka C9orf26, DVS27, IL1F11, NF-HEV, NFEHEV}, IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, TRBV20OR9-2 (T cell receptor beta variable 20/OR9-2 (non-functional)) [NCBI Gene 6962] {aka CDR3, TCRBV20S2, TCRBV2O, TCRBV2S2O}, TSLP (thymic stromal lymphopoietin) [NCBI Gene 85480], CRLF2 (cytokine receptor like factor 2) [NCBI Gene 64109] {aka CRL2, CRLF2Y, TSLPR}, TNFSF4 (TNF superfamily member 4) [NCBI Gene 7292] {aka CD134L, CD252, GP34, OX-40L, OX4OL, TNLG2B}, TNFRSF4 (TNF receptor superfamily member 4) [NCBI Gene 7293] {aka ACT35, CD134, IMD16, OX40, TXGP1L}
- **Diseases:** infections (MESH:D007239), HP (MESH:C537262), inflammation (MESH:D007249), Gastrointestinal symptoms (MESH:D012817), Bacterial (MESH:D001424), injury to (MESH:D014947), rhinitis (MESH:D012220), immune dysregulation (OMIM:614878), CMPA (MESH:D016269), urticaria (MESH:D014581), endotoxemia (MESH:D019446), atopic (MESH:C566404), atopic dermatitis (MESH:D003876), abdominal bloating (MESH:D000007), impaired gastrointestinal motility (MESH:D005767), allergic rhinitis (MESH:D065631), facial erythema (MESH:D004890), IBS (MESH:D053560), hyperplasia (MESH:D006965), dysbiosis (MESH:D064806), CSU (MESH:D000080223), atopy (MESH:C564133), cell (MESH:D002292), CAP (MESH:D015746), asthmatic (MESH:D013224), pruritus (MESH:D011537), atopic asthma (MESH:C565292), pain (MESH:D010146), H. pylori infection (MESH:D016481), SIBO (MESH:D001765), motility disturbances (MESH:D015154), allergic (MESH:D004342), FA (MESH:D005512), constipation (MESH:D003248), diarrhea (MESH:D003967), Atopic Disorders (MESH:D006969), MCAS (MESH:D000090267), Asthma (MESH:D001249), edema (MESH:D004487)
- **Chemicals:** GBT (-), H2 (MESH:D006859), histamine (MESH:D006632), CH4 (MESH:D008697), urea (MESH:D014508), luminal (MESH:D010634), glucose (MESH:D005947), LPS (MESH:D008070), rifaximin (MESH:D000078262), SCFA (MESH:D005232), lactulose (MESH:D007792)
- **Species:** Proteus (genus) [taxon 210425], Helicobacter pylori (species) [taxon 210], Enterobacteriaceae (enterobacteria, family) [taxon 543], Klebsiella (genus) [taxon 570], Escherichia coli (E. coli, species) [taxon 562], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** M16V

## Full text

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## Figures

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## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12940673/full.md

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Source: https://tomesphere.com/paper/PMC12940673