# Effects of a combination of bifidobacteria quadruple viable bacteria tablets and quadruple therapy on inflammatory response and Helicobacter pylori eradication rate in patients with Helicobacter pylori positive gastric ulcers

**Authors:** Chunying Jiang, Jing Shi, Xinfu Zhuang, Meng Zhou, Haiyan Zhong

PMC · DOI: 10.3389/fmed.2025.1636039 · Frontiers in Medicine · 2025-09-29

## TL;DR

Adding bifidobacteria tablets to standard treatment for Helicobacter pylori improves symptoms, eradication rates, and immune function in patients with gastric ulcers.

## Contribution

This study demonstrates that combining bifidobacteria with quadruple therapy enhances treatment outcomes for Helicobacter pylori-positive gastric ulcers.

## Key findings

- The study group had a higher Helicobacter pylori eradication rate and improved clinical symptoms compared to the control group.
- Levels of inflammatory markers like IL-6, CRP, and MMP-9 were significantly reduced in the study group.
- The study group showed increased beneficial gut bacteria and improved immune function with fewer adverse reactions.

## Abstract

To explore the effects of bifidobacteria quadruple viable bacteria tablets (Bifidobacterium infantis, Lactobacillus acidophilus, Enterococcus faecalis, and Bacillus cereus) plus quadruple therapy on inflammatory response and Helicobacter pylori (Hp) eradication rate in patients with Hp-positive gastric ulcers.

One hundred patients with Hp-positive gastric ulcers admitted in our hospital from January 2022 to December 2024 were included and divided into a control group and a study group. The former accepted quadruple therapy (esomeprazole magnesium enteric-coated capsules + colloidal bismuth pectin capsule + clarithromycin tablets + amoxicillin capsule). Based on the quadruple therapy, the latter was added with bifidobacteria quadruple viable bacteria tablets. The clinical symptoms, clinical efficacy, Hp eradication rate, levels of gastrointestinal hormones and inflammatory factors, immune function, number of beneficial bacteria, and incidence of adverse reactions were compared in both groups.

Following 2 weeks of treatment, the study group had lower scores across these symptoms compared to the control group (P < 0.05). Furthermore, the study group had a higher total treatment efficacy rate and a higher Hp eradication rate compared to the control group (P < 0.05). Compared to the control group, the study group had higher levels of serum somatostatin and lower levels of motilin, gastrin, and pepsinogen I following 2 weeks of treatment (P < 0.05). Additionally, the study group had lower levels of interleukin-6 (IL-6), C-reactive protein (CRP), interleukin-8 (IL-8), and matrix metalloproteinase-9 (MMP-9) compared to the control group (P < 0.05). In comparison to the control group, the study group had higher levels of CD4 + T-cells, higher CD4 + /CD8 + ratio and lower CD8 + T-cell levels after 2 weeks of treatment (P < 0.05). Moreover, the study group had a significant increase in the abundance of beneficial gut microbiota, specifically Enterococcus faecalis, Lactobacillus acidophilus, and Bifidobacterium compared to the control group (P < 0.05). Lastly, the study group had a lower incidence of adverse reactions than the control group (P < 0.05).

Bifidobacteria quadruple viable bacteria tablets plus quadruple therapy can improve the clinical symptoms, promote the clinical therapeutic effect and Hp eradication rate, improve the levels of gastrointestinal hormones and inflammatory factors, enhance the immune function, increase levels of beneficial bacteria and diminish the incidence of adverse reactions caused by quadruple therapy in patients suffered from Hp-positive gastric ulcer.

## Linked entities

- **Chemicals:** esomeprazole magnesium (PubChem CID 130564), clarithromycin (PubChem CID 84029), amoxicillin (PubChem CID 33613)
- **Species:** Lactobacillus acidophilus (taxon 1579), Enterococcus faecalis (taxon 1351), Bacillus cereus (taxon 1396)

## Full-text entities

- **Genes:** MLN (motilin) [NCBI Gene 4295], IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, SST (somatostatin) [NCBI Gene 6750] {aka SMST, SST1}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, GAST (gastrin) [NCBI Gene 2520] {aka GAS}
- **Diseases:** inflammatory (MESH:D007249), gastric ulcer (MESH:D013276)
- **Chemicals:** clarithromycin (MESH:D017291), amoxicillin (MESH:D000658), esomeprazole (MESH:D064098), Bifidobacteria (-), magnesium (MESH:D008274)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Helicobacter pylori (species) [taxon 210], Lactobacillus acidophilus (species) [taxon 1579], Bacillus cereus (species) [taxon 1396], Enterococcus faecalis (species) [taxon 1351], Bifidobacterium longum subsp. infantis (subspecies) [taxon 1682], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12515940/full.md

## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12515940/full.md

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Source: https://tomesphere.com/paper/PMC12515940