Blood Microbiome Reveals the Impact of Lactobacillus on the Efficacy of Immunotherapy in Gastrointestinal Cancer

Ya-Shang Zheng , Wu-Hao Lin , Jun-Quan Chen , Xiao-Li Wei , Jia-Qian Huang , Yu-Hong Xu , Meng Yang , Qi-Hua Zhang , Zhi-Jun Zuo , Zhao-Ying Yang , Pan Zhang , Nga Ki HONG , Lu-Xuan Liu , Zhao-Lei Zeng , Rui-Hua Xu , Hui-Yan Luo

MedComm ›› 2025, Vol. 6 ›› Issue (8) : e70316

PDF
MedComm ›› 2025, Vol. 6 ›› Issue (8) : e70316 DOI: 10.1002/mco2.70316
ORIGINAL ARTICLE

Blood Microbiome Reveals the Impact of Lactobacillus on the Efficacy of Immunotherapy in Gastrointestinal Cancer

Author information +
History +
PDF

Abstract

Immunotherapy has revolutionized the treatment of gastrointestinal (GI) cancers, but reliable biomarkers for predicting treatment efficacy remain limited. In this study, we explored the potential of blood microbiome and specific microbial taxa as novel biomarkers for predicting the efficacy of immunotherapy combined with chemotherapy in GI cancer patients through 16S rRNA sequencing. Our findings demonstrated that lower baseline alpha diversity and specific microbial compositions, particularly lower levels of Lactobacillus, were significantly associated with longer progression-free survival (PFS) in patients receiving immunotherapy combined with chemotherapy. Furthermore, we validated the reliability of Lactobacillus abundance as a predictor of PFS and treatment response in another independent patient cohort. Additionally, patients with increased or stable levels of Lactobacillus after immunotherapy combined with chemotherapy had superior PFS. Gavage of Lactobacillus rhamnosus (L. rhamnosus) el evated its blood level and enhanced the efficacy of immunotherapy in mouse models. Our results suggest that Lactobacillus may serve as a novel biomarker for predicting the efficacy of immunotherapy combined with chemotherapy and hold the potential as a PD-1 antibody sensitizer.

Keywords

biomarker / blood microbiome / efficacy / immunotherapy / Lactobacillus

Cite this article

Download citation ▾
Ya-Shang Zheng, Wu-Hao Lin, Jun-Quan Chen, Xiao-Li Wei, Jia-Qian Huang, Yu-Hong Xu, Meng Yang, Qi-Hua Zhang, Zhi-Jun Zuo, Zhao-Ying Yang, Pan Zhang, Nga Ki HONG, Lu-Xuan Liu, Zhao-Lei Zeng, Rui-Hua Xu, Hui-Yan Luo. Blood Microbiome Reveals the Impact of Lactobacillus on the Efficacy of Immunotherapy in Gastrointestinal Cancer. MedComm, 2025, 6(8): e70316 DOI:10.1002/mco2.70316

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

F. Bray, M. Laversanne, H. Sung, et al., “Global Cancer Statistics 2022: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries,” CA: A Cancer Journal for Clinicians 74, no. 3 (2024): 229-263.

[2]

L. H. Biller and D. Schrag, “Diagnosis and Treatment of Metastatic Colorectal Cancer: A Review,” JAMA 325, no. 7 (2021): 669-685.

[3]

F. Lordick, F. Carneiro, S. Cascinu, et al., “Gastric Cancer: ESMO Clinical Practice Guideline for Diagnosis, Treatment and Follow-Up,” Annals of Oncology 33, no. 10 (2022): 1005-1020.

[4]

X. Wang, P. Wang, X. Huang, Y. Han, P. Zhang, “Biomarkers for Immunotherapy in Esophageal Cancer,” Frontiers in Immunology 14 (2023): 1117523.

[5]

Y. Doki, J. A. Ajani, K. Kato, et al., “Nivolumab Combination Therapy in Advanced Esophageal Squamous-Cell Carcinoma,” New England Journal of Medicine 386, no. 5 (2022): 449-462.

[6]

Z. X. Wang, C. Cui, J. Yao, et al., “Toripalimab Plus Chemotherapy in Treatment-Naïve, Advanced Esophageal Squamous Cell Carcinoma (JUPITER-06): A Multi-Center Phase 3 Trial,” Cancer Cell 40, no. 3 (2022): 277-288.e3.

[7]

Y. Y. Janjigian, K. Shitara, M. Moehler, et al., “First-Line Nivolumab Plus Chemotherapy Versus Chemotherapy Alone for Advanced Gastric, Gastro-Oesophageal Junction, and Oesophageal Adenocarcinoma (CheckMate 649): A Randomised, Open-Label, Phase 3 Trial,” Lancet 398, no. 10294 (2021): 27-40.

[8]

W. L. Guan, Y. He, and R. H. Xu, “Gastric Cancer Treatment: Recent Progress and Future Perspectives,” Journal of Hematology & Oncology 16, no. 1 (2023): 57.

[9]

Y. K. Kang, L. T. Chen, M. H. Ryu, et al., “Nivolumab Plus Chemotherapy Versus Placebo Plus Chemotherapy in Patients With HER2-Negative, Untreated, Unresectable Advanced or Recurrent Gastric or Gastro-Oesophageal Junction Cancer (ATTRACTION-4): A Randomised, Multicentre, Double-Blind, Placebo-Controlled, Phase 3 Trial,” Lancet Oncology 23, no. 2 (2022): 234-247.

[10]

J. Taieb, M. Svrcek, R. Cohen, et al., “Deficient Mismatch Repair/Microsatellite Unstable Colorectal Cancer: Diagnosis, Prognosis and Treatment,” European Journal of Cancer 175 (2022): 136-157.

[11]

D. C. Guven, G. Kavgaci, E. Erul, et al., “The Efficacy of Immune Checkpoint Inhibitors in Microsatellite Stable Colorectal Cancer: A Systematic Review,” Oncologist 29, no. 5 (2024): e580-e600.

[12]

D. B. Doroshow, S. Bhalla, M. B. Beasley, et al., “PD-L1 as a Biomarker of Response to Immune-Checkpoint Inhibitors,” Nature Reviews Clinical Oncology 18, no. 6 (2021): 345-362.

[13]

Z. Zhang, J. Huang, Y. Xu, and H. Luo, “Chemoimmunotherapy for Esophageal Squamous Cell Carcinoma—Summary and Discussion of Recent Clinical Trials,” MedComm—Future Medicine 2, no. 3 (2023): e56.

[14]

M. J. Overman, S. Lonardi, K. Wong, et al., “Durable Clinical Benefit With Nivolumab Plus Ipilimumab in DNA Mismatch Repair-Deficient/Microsatellite Instability-High Metastatic Colorectal Cancer,” Journal of Clinical Oncology 36, no. 8 (2018): 773-779.

[15]

A. Marabelle, M. Fakih, J. Lopez, et al., “Association of Tumour Mutational Burden With Outcomes in Patients With Advanced Solid Tumours Treated With Pembrolizumab: Prospective Biomarker Analysis of the Multicohort, Open-Label, Phase 2 KEYNOTE-158 Study,” Lancet Oncology 21, no. 10 (2020): 1353-1365.

[16]

K. Li, A. Zhang, X. Li, H. Zhang, and L. Zhao, “Advances in Clinical Immunotherapy for Gastric Cancer,” Biochimica et Biophysica Acta. Reviews on Cancer 1876, no. 2 (2021): 188615.

[17]

W. Zhao, L. Jin, P. Chen, et al., “Colorectal Cancer Immunotherapy-Recent Progress and Future Directions,” Cancer Letters 545 (2022): 215816.

[18]

B. Routy, E. Le Chatelier, L. Derosa, et al., “Gut Microbiome Influences Efficacy of PD-1-Based Immunotherapy Against Epithelial Tumors,” Science 359, no. 6371 (2018): 91-97.

[19]

Z. Peng, S. Cheng, Y. Kou, et al., “The Gut Microbiome Is Associated With Clinical Response to Anti-PD-1/PD-L1 Immunotherapy in Gastrointestinal Cancer,” Cancer Immunology Research 8, no. 10 (2020): 1251-1261.

[20]

S. Fan, W. Zhang, L. Zhou, D. Wang, and D. Tang, “Potential Role of the Intratumoral Microbiota in Colorectal Cancer Immunotherapy,” International Immunopharmacology 137 (2024): 112537.

[21]

N. Zmora, J. Suez, and E. Elinav, “You Are What You Eat: Diet, Health and the Gut Microbiota,” Nature Reviews Gastroenterology & Hepatology 16, no. 1 (2019): 35-56.

[22]

S. Pushalkar, M. Hundeyin, D. Daley, et al., “The Pancreatic Cancer Microbiome Promotes Oncogenesis by Induction of Innate and Adaptive Immune Suppression,” Cancer Discovery 8, no. 4 (2018): 403-416.

[23]

L. Zitvogel, R. Daillère, M. P. Roberti, B. Routy, and G. Kroemer, “Anticancer Effects of the Microbiome and Its Products,” Nature Reviews Microbiology 15, no. 8 (2017): 465-478.

[24]

D. Nejman, I. Livyatan, G. Fuks, et al., “The Human Tumor Microbiome Is Composed of Tumor Type-Specific Intracellular Bacteria,” Science 368, no. 6494 (2020): 973-980.

[25]

L. T. Geller, M. Barzily-Rokni, T. Danino, et al., “Potential Role of Intratumor Bacteria in Mediating Tumor Resistance to the Chemotherapeutic Drug Gemcitabine,” Science 357, no. 6356 (2017): 1156-1160.

[26]

X. Zhou, L. You, Z. Xin, et al., “Leveraging Circulating Microbiome Signatures to Predict Tumor Immune Microenvironment and Prognosis of Patients With Non-Small Cell Lung Cancer,” Journal of Translational Medicine 21, no. 1 (2023): 800.

[27]

K. J. Ouaknine, D. T. P. Helly, C. Dumenil, et al., “Role of Antibiotic Use, Plasma Citrulline and Blood Microbiome in Advanced Non-Small Cell Lung Cancer Patients Treated With Nivolumab,” Journal for ImmunoTherapy of Cancer 7, no. 1 (2019): 176.

[28]

D. Yang, X. Wang, X. Zhou, et al., “Blood Microbiota Diversity Determines Response of Advanced Colorectal Cancer to Chemotherapy Combined With Adoptive T Cell Immunotherapy,” Oncoimmunology 10, no. 1 (2021): 1976953.

[29]

X. Chong, Y. Madeti, J. Cai, et al., “Recent Developments in Immunotherapy for Gastrointestinal Tract Cancers,” Journal of Hematology & Oncology 17, no. 1 (2024): 65.

[30]

J. Huang, Y. Mao, and L. Wang, “The Crosstalk of Intratumor Bacteria and the Tumor,” Frontiers in Cellular and Infection Microbiology 13 (2023): 1273254.

[31]

B. A. Helmink, M. Khan, A. Hermann, V. Gopalakrishnan, J. A. Wargo, “The Microbiome, Cancer, and Cancer Therapy,” Nature Medicine 25, no. 3 (2019): 377-388.

[32]

S. Y. Lee, J. Jhun, J. S. Woo, et al., “Gut Microbiome-Derived Butyrate Inhibits the Immunosuppressive Factors PD-L1 and IL-10 in Tumor-Associated Macrophages in Gastric Cancer,” Gut Microbes 16, no. 1 (2024): 2300846.

[33]

H. J. Jang, J. Y. Choi, K. Kim, et al., “Relationship of the Lung Microbiome With PD-L1 Expression and Immunotherapy Response in Lung Cancer,” Respiratory Research 22, no. 1 (2021): 322.

[34]

V. Gopalakrishnan, C. N. Spencer, L. Nezi, et al., “Gut Microbiome Modulates Response to Anti-PD-1 Immunotherapy in Melanoma Patients,” Science 359, no. 6371 (2018): 97-103.

[35]

X. Yu, W. Li, Z. Li, Q. Wu, and S. Sun, “Influence of Microbiota on Tumor Immunotherapy,” International Journal of Biological Sciences 20, no. 6 (2024): 2264-2294.

[36]

D. Dora, B. Ligeti, T. Kovacs, et al., “Non-Small Cell Lung Cancer Patients Treated With Anti-PD1 Immunotherapy Show Distinct Microbial Signatures and Metabolic Pathways According to Progression-Free Survival and PD-L1 Status,” Oncoimmunology 12, no. 1 (2023): 2204746.

[37]

Z. Zhang, Y. Qiu, H. Feng, et al., “Identification of Malassezia Globosa as a Gastric Fungus Associated With PD-L1 Expression and Overall Survival of Patients With Gastric Cancer,” Journal of Immunology Research 2022 (2022): 2430759.

[38]

B. A. Friend and K. M. Shahani, “Antitumor Properties of Lactobacilli and Dairy Products Fermented by Lactobacilli,” Journal of Food Protection 47, no. 9 (1984): 717-723.

[39]

F. Xu, Q. Li, S. Wang, et al., “The Efficacy of Prevention for Colon Cancer Based on the Microbiota Therapy and the Antitumor Mechanisms With Intervention of Dietary Lactobacillus,” Microbiology Spectrum 11, no. 5 (2023): e0018923.

[40]

C. Mantegazza, P. Molinari, E. D'Auria, et al., “Probiotics and Antibiotic-Associated Diarrhea in Children: A Review and New Evidence on Lactobacillus rhamnosus GG During and After Antibiotic Treatment,” Pharmacological Research 128 (2018): 63-72.

[41]

S. K. Han, Y. J. Shin, D. Y. Lee, et al., “Lactobacillus Rhamnosus HDB1258 Modulates Gut Microbiota-Mediated Immune Response in Mice With or Without Lipopolysaccharide-Induced Systemic Inflammation,” BMC Microbiology 21, no. 1 (2021): 146.

[42]

L. F. Mager, R. Burkhard, N. Pett, et al., “Microbiome-Derived Inosine Modulates Response to Checkpoint Inhibitor Immunotherapy,” Science 369, no. 6510 (2020): 1481-1489.

[43]

Y. Wang, X. Zhang, J. Li, et al., “Sini Decoction Ameliorates Colorectal Cancer and Modulates the Composition of Gut Microbiota in Mice,” Frontiers in Pharmacology 12 (2021): 609992.

[44]

A. Abedin-Do, Z. Taherian-Esfahani, S. Ghafouri-Fard, S. Ghafouri-Fard, and E. Motevaseli, “Immunomodulatory Effects of Lactobacillus Strains: Emphasis on Their Effects on Cancer Cells,” Immunotherapy 7, no. 12 (2015): 1307-1329.

[45]

D. L. A. de Moreno, C. Matar, C. Thériault, and G. Perdigón, “Effects of Milk Fermented by Lactobacillus helveticus R389 on Immune Cells Associated to Mammary Glands in Normal and a Breast Cancer Model,” Immunobiology 210, no. 5 (2005): 349-358.

[46]

H. Chon, B. Choi, E. Lee, S. Lee, and G. Jeong, “Immunomodulatory Effects of Specific Bacterial Components of Lactobacillus plantarum KFCC11389P on the Murine Macrophage Cell Line RAW 264.7,” Journal of Applied Microbiology 107, no. 5 (2009): 1588-1597.

[47]

S. Pathmakanthan, C. K. Li, J. Cowie, and C. J. Hawkey, “Lactobacillus plantarum 299: Beneficial in Vitro Immunomodulation in Cells Extracted From Inflamed Human Colon,” Journal of Gastroenterology and Hepatology 19, no. 2 (2004): 166-173.

[48]

J. Escamilla, M. A. Lane, and V. Maitin, “Cell-Free Supernatants From Probiotic Lactobacillus casei and Lactobacillus rhamnosus GG Decrease Colon Cancer Cell Invasion In Vitro,” Nutrition and Cancer 64, no. 6 (2012): 871-878.

RIGHTS & PERMISSIONS

2025 The Author(s). MedComm published by Sichuan International Medical Exchange & Promotion Association (SCIMEA) and John Wiley & Sons Australia, Ltd.

AI Summary AI Mindmap
PDF

12

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/