Skip to content
DraconiticResearch
Search Sources API
197,785 studies31 sourcesUpdated 54 min ago
Peer-reviewedCC BY 4.0Frontiers in Immunology

Jiangshui-derived Lactobacillus plantarum GR-4 enhances the therapeutic efficacy of PD-1/PD-L1 inhibitors against gastric cancer

5 affiliations
  1. 1Department of Oncology, The Second Hospital & Clinical Medical School, Lanzhou University
  2. 2Departments of Orthopedics, The Second Hospital & Clinical Medical School, Lanzhou University
  3. 3Centre for Grassland Microbiome, State Key Laboratory of Herbage Improvement and Grassland Agro-ecosystems, College of Pastoral Agricultural Science and Technology, Lanzhou University
  4. 4Ministry of Education Key Laboratory of Cell Activities and Stress Adaptations, School of Life Sciences, Lanzhou University
  5. 5The Second Hospital & Clinical Medical School, Lanzhou University

Abstract

Objective: To investigate whether the Jiangshui-derived probiotic Lactobacillus plantarum GR-4 can enhance gastric cancer sensitivity to PD-1 inhibitors and reshape the tumor immune microenvironment.

Methods: A mouse gastric cancer model was established. Mice received oral GR-4 monotherapy, PD-1 blocking antibody monotherapy, or combined GR-4 and PD-1 antibody treatment. In vivo antitumor efficacy was evaluated by measuring tumor weight. We assessed CD8 ⁺ T-cell infiltration, cytokines related to T-cell activation and differentiation, and the expression of the activation marker CD69 on CD3 ⁺ /CD8 ⁺ T cells within tumor tissues. 16S rRNA sequencing of gut microbiota and fecal metabolomic analysis were performed to explore the regulatory effects of GR-4 on gut microbiota composition and metabolic profiles. In vitro , human gastric cancer BGC-823 cells were treated with GR-4 combined with PD-1 intervention, and transcriptome sequencing was applied to further validate the underlying molecular regulatory mechanisms.

Results: In vivo results demonstrated that combined GR-4 and PD-1 antibody treatment exerted prominent synergistic antitumor activity, effectively suppressing tumor growth while markedly mitigating PD-1-associated body weight loss (p < 0.01). Further assays revealed that GR-4 synergistically elevated tumor-infiltrating CD3 ⁺ /CD8 ⁺ T-cell levels and upregulated CD69 expression on these cells, thereby remodelling the tumor immune microenvironment. Additionally, GR-4, whether administered alone or combined with PD-1 antibody, optimized gut microbiota structure, increased the abundance of probiotic genera including Ligilactobacillus and Bacteroides , reversed intestinal metabolic disturbances, and raised the levels of short-chain fatty-acid-related metabolites such as ethoxyacetic acid and 2,5-dihydroxybenzoic acid. Transcriptomic sequencing showed significant enrichment of the PD-1 checkpoint pathway in the GR-4 group versus Ctrl (p=0.01), whereas no significant enrichment was observed between the PD-1 inhibitor group and GR-4/PD-1 inhibitor group (p=0.14).

Conclusion: This study is the first to confirm that Lactobacillus plantarum GR-4 synergizes with PD-1 inhibitors to restrain gastric cancer progression via T-cell activation and elevated intratumoral T-cell infiltration. These findings provide novel theoretical evidence and a potential combinatorial immunotherapeutic strategy for gastric cancer.

Related

  1. Chickpea flour (Cicer arietinum L) improves viability of potentially probiotics Lactobacillus plantarum S180.7 and Lactobacillus plantarum SBR64.7 in milk-based formulations
    Larissa Dos Santos Freitas, Sandra Fernandes Arruda, Maria Carolina Mesquita +2
    PLOS OnePeer-reviewedCC BYFull textEnzymology & metabolismMicrobiologyPLOSEurope PMCPMC
  2. A multi-omics characterization of the gut microbiota of weaned piglets in response to Lactobacillus plantarum supplementation.
    Nae-Ho Park, Byeonghwi Lim, Chiwoong Lim +9
    Journal of animal science and technologyPeer-reviewedCC BY-NCFull textZoology & animal behaviourEurope PMC
  3. Anti-inflammatory effects of vitamin K2 and Lactobacillus plantarum in a mouse model of colorectal cancer
    Magdalena Strus, Aleksandra Wójcik, Alicja M. Gruszka +13
    BMC BiologyPeer-reviewedCC BY 4.0Molecular biology & gene regulationGeneral biologyCrossref
  4. Co-inoculation with Lactiplantibacillus plantarum and Bacillus amyloliquefaciens enhances the fermentation quality and in vitro ruminal digestibility of whole-plant millet silage
    Shanshan He, Shiteng Pei, Liangkang Lv +6
    Scientific ReportsPeer-reviewedCC BY-NC-ND 4.0Full textPlant biologyCrossref
  5. Widening the BRCAness therapeutic window for its synthetic lethality effects with PARP inhibitors
    Anthony Fernandez, Yuvika Salman, Roxanne Castillo +2
    Communications BiologyPeer-reviewedCC BY-NC-ND 4.0Full textGeneral biologyNatureCrossrefEurope PMCPMC
BibTeX
@article{wang2026jiangshuiderived,
  title = {{Jiangshui-derived Lactobacillus plantarum GR-4 enhances the therapeutic efficacy of PD-1/PD-L1 inhibitors against gastric cancer}},
  author = {Na Wang and Kai Wang and Huawen Han and Jingwen Fan and Feixue Song and Hao Chen and Xiangkai Li},
  journal = {Frontiers in Immunology},
  year = {2026},
  month = oct,
  doi = {10.3389/fimmu.2026.1987320},
  url = {https://www.frontiersin.org/articles/10.3389/fimmu.2026.1987320/full},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Jiangshui-derived Lactobacillus plantarum GR-4 enhances the therapeutic efficacy of PD-1/PD-L1 inhibitors against gastric cancer
AU  - Na Wang
AU  - Kai Wang
AU  - Huawen Han
AU  - Jingwen Fan
AU  - Feixue Song
AU  - Hao Chen
AU  - Xiangkai Li
PY  - 2026
DA  - 2026/10/29
JO  - Frontiers in Immunology
DO  - 10.3389/fimmu.2026.1987320
UR  - https://www.frontiersin.org/articles/10.3389/fimmu.2026.1987320/full
AB  - Objective: To investigate whether the Jiangshui-derived probiotic Lactobacillus plantarum GR-4 can enhance gastric cancer sensitivity to PD-1 inhibitors and reshape the tumor immune microenvironment.  Methods: A mouse gastric cancer model was established. Mice received oral GR-4 monotherapy, PD-1 blocking antibody monotherapy, or combined GR-4 and PD-1 antibody treatment. In vivo antitumor efficacy was evaluated by measuring tumor weight. We assessed CD8 ⁺ T-cell infiltration, cytokines related to T-cell activation and differentiation, and the expression of the activation marker CD69 on CD3 ⁺ /CD8 ⁺ T cells within tumor tissues. 16S rRNA sequencing of gut microbiota and fecal metabolomic analysis were performed to explore the regulatory effects of GR-4 on gut microbiota composition and metabolic profiles. In vitro , human gastric cancer BGC-823 cells were treated with GR-4 combined with PD-1 intervention, and transcriptome sequencing was applied to further validate the underlying molecular regulatory mechanisms.  Results: In vivo results demonstrated that combined GR-4 and PD-1 antibody treatment exerted prominent synergistic antitumor activity, effectively suppressing tumor growth while markedly mitigating PD-1-associated body weight loss (p < 0.01). Further assays revealed that GR-4 synergistically elevated tumor-infiltrating CD3 ⁺ /CD8 ⁺ T-cell levels and upregulated CD69 expression on these cells, thereby remodelling the tumor immune microenvironment. Additionally, GR-4, whether administered alone or combined with PD-1 antibody, optimized gut microbiota structure, increased the abundance of probiotic genera including Ligilactobacillus and Bacteroides , reversed intestinal metabolic disturbances, and raised the levels of short-chain fatty-acid-related metabolites such as ethoxyacetic acid and 2,5-dihydroxybenzoic acid. Transcriptomic sequencing showed significant enrichment of the PD-1 checkpoint pathway in the GR-4 group versus Ctrl (p=0.01), whereas no significant enrichment was observed between the PD-1 inhibitor group and GR-4/PD-1 inhibitor group (p=0.14).  Conclusion: This study is the first to confirm that Lactobacillus plantarum GR-4 synergizes with PD-1 inhibitors to restrain gastric cancer progression via T-cell activation and elevated intratumoral T-cell infiltration. These findings provide novel theoretical evidence and a potential combinatorial immunotherapeutic strategy for gastric cancer.
SN  - 1664-3224
ER  -