# Immune Modulation Through Long‐Term Lacticaseibacillus rhamnosus Therapy in Home Mechanically Ventilated Patients

**Authors:** Kamila Szyller, Grazyna Mlynarczyk, Beata Mlynarczyk‐Bonikowska, Janusz Sierdzinski, Joanna Styk, Michal Marusza, Wojciech Marusza

PMC · DOI: 10.1002/mbo3.70113 · MicrobiologyOpen · 2025-11-05

## TL;DR

Long-term use of Lacticaseibacillus rhamnosus GG in home ventilated patients boosts immune markers like IL-2 and IFN-γ, potentially reducing infection risk.

## Contribution

This is the first study to investigate LGG's immune-modulating effects in home mechanically ventilated patients.

## Key findings

- LGG supplementation significantly increased IL-2 levels at 3 and 6 months.
- IFN-γ and IL-4 levels also rose temporarily, suggesting immune system modulation.
- No antibiotic use was needed during the intervention period, unlike previous seasons.

## Abstract

The beneficial effects of probiotics on the immune system are well established; however, the precise mechanisms underlying their action remain incompletely understood. To date, the impact of probiotics in home mechanically ventilated (HMV) patients has not been investigated. This study evaluated the effects of oral supplementation with Lacticaseibacillus rhamnosus GG ATCC 53103 (LGG) on nasal microbiota composition and selected immune parameters in HMV patients. Thirty‐one individuals, following a 3‐month probiotic‐free washout period, received LGG at a dose of 8 × 109 CFU/day for 6 months. Nasal swabs and blood samples were collected at baseline, and after 3 and 6 months, to assess nasal microflora, Th1/Th2 balance, and levels of IL‐2, IL‐4, IL‐5, IL‐10, TNF‐α, and IFN‐γ. A statistically significant increase in IL‐2 was observed at both 3 and 6 months (p = 0.0307; p = 0.0001, respectively), along with a transient rise in IFN‐γ at 3 months (p = 0.0253) and IL‐4 at 6 months (p = 0.0297). The IFN‐γ/IL‐10 ratio also increased at 3 months (p = 0.0394). No significant changes were detected in the remaining cytokines or nasal bacterial flora. Notably, none of the participants required antibiotic therapy during the intervention period—contrasting with prior seasons, when at least one course was typically necessary. Given the critical role of IL‐2 and IFN‐γ in anti‐infective immunity, their elevation may indicate enhanced resistance to infection, while increased IL‐4 may reflect modulation of inflammation. These findings suggest that LGG supplementation, due to its safety, affordability, and immunomodulatory potential, may be a valuable adjunctive strategy to reduce infection risk and improve outcomes in HMV patients.

Antibiotic resistance crisis drives the search for innovative antibacterial solutions. Probiotics, particularly Lacticaseibacillus rhamnosus GG ATCC 53103 (LGG), show promise in preventing bacterial infections and reducing antibiotic use. LGG has well‐documented health benefits and can strengthen the immune system, especially in chronically ill patients. Probiotic supplementation in farm animals stabilizes microbiota and reduces antibiotic dependence. Home mechanical ventilation (HMV) patients face high infection risks, yet LGG's immune benefits in this group remain understudied. This study demonstrates that long‐term LGG therapy enhances immune parameters, particularly by increasing IL‐2 levels. LGG therapy is a cost‐effective and accessible option for improving immunity in HMV patients.

## Linked entities

- **Proteins:** IL2 (interleukin 2), IL4 (interleukin 4), IL5 (interleukin 5), IL10 (interleukin 10), TNF (tumor necrosis factor), IFNG (interferon gamma)

## Full-text entities

- **Genes:** IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}
- **Diseases:** infection (MESH:D007239), inflammation (MESH:D007249)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12587047/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12587047/full.md

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Source: https://tomesphere.com/paper/PMC12587047