Evidence map›Paper›PMID 41574027›Full record

ReviewMedComm2026

Tumor Immunotherapy and Microbiome: From Bench-to-Bedside Applications.

Anqi Lin, Minying Xiong, Aimin Jiang, Li Chen, Lihaoyun Huang, Kailai Li, Hank Z H Wong, Jian Zhang, Zaoqu Liu, Quan Cheng and 3 more

Abstract readReview
In one paragraph

Review in MedComm, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Programming the tumor microenvironment through microbiome-driven mechanisms.Frontiers in cellular and infection microbiology · 2026
    Review
  6. Review
  7. Review
  8. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Anqi LinDepartment of Oncology Zhujiang Hospital, Southern Medical University Guangzhou China.
Minying XiongDepartment of Oncology Zhujiang Hospital, Southern Medical University Guangzhou China.
Aimin JiangDepartment of Urology Changhai Hospital, Naval Medical University (Second Military Medical University) Shanghai China.
Li ChenCancer Centre and Institute of Translational Medicine, Faculty of Health Sciences University of Macau Macau SAR China.
Lihaoyun HuangDepartment of Oncology Zhujiang Hospital, Southern Medical University Guangzhou China.
Kailai LiDepartment of Oncology Zhujiang Hospital, Southern Medical University Guangzhou China.
Hank Z H WongLi Ka Shing Faculty of Medicine The University of Hong Kong Hong Kong SAR China.
Jian ZhangDepartment of Oncology Zhujiang Hospital, Southern Medical University Guangzhou China.
Zaoqu LiuInstitute of Basic Medical Sciences Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China.
Quan ChengDepartment of Neurosurgery Xiangya Hospital, Central South University Changsha China.
Bufu TangDepartment of Interventional Radiology Zhongshan Hospital, Fudan University Shanghai China.
Pengpeng ZhangDepartment of Lung Cancer Tianjin Lung Cancer Center National Clinical Research Center for Cancer Key Laboratory of Cancer Prevention and Therapy Tianjin's Clinical Research Center for Cancer Tianjin Medical University Cancer Institute and Hospital Tianjin China.ORCID https://orcid.org/0000-0003-1488-265X
Peng LuoDepartment of Oncology Zhujiang Hospital, Southern Medical University Guangzhou China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer immunotherapy has emerged as a transformative therapeutic strategy that harnesses the immune system to combat malignant tumors, overcoming critical limitations such as the nonspecific cytotoxicity of conventional chemotherapy and radiotherapy and drug resistance arising from target mutations in targeted therapies. Growing evidence demonstrates that the human microbiome plays a pivotal role in modulating immune responses and influencing the efficacy of immunotherapeutic interventions. Although the impact is increasingly recognized, the molecular mechanisms and translational potential of microbiome-based strategies remain incompletely explored. This review systematically elucidates how microorganisms from distinct anatomical sites (including bacteria, fungi, and viruses residing in the gut, oral cavity, skin, respiratory tract, and urogenital tract) and intratumoral microbes modulate the tumor immune microenvironment through metabolites, immune cell priming, and antigen mimicry. Furthermore, we discuss how specific microbial signatures predict responses to immune checkpoint inhibitors (ICIs) and CAR-T cell therapy, and highlight emerging interventional strategies, including fecal microbiome transplantation (FMT), probiotics, and engineered bacteria, that demonstrate synergistic effects with immunotherapy in preclinical and clinical settings. By integrating mechanistic insights with translational advances, this review provides a comprehensive scientific foundation for microbiome-based precision immunotherapy, aimed at improving patient survival outcomes and reducing treatment-related adverse events.

Indexed as

cancerimmune checkpoint inhibitorsimmunotherapymicrobiometumor microenvironment

Identifiers

PMID41574027
PMCPMC12820422

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.