Evidence map›Paper›PMID 40597177›Full record

ArticleBMC medicine2025

Faecalibacterium prausnitzii promotes anti-PD-L1 efficacy in natural killer/T-cell lymphoma by enhancing antitumor immunity.

Zhuangzhuang Shi, Wenxing Jiang, Hongwen Li, Yue Zhang, Weili Xue, Yingjun Wang, Mingzhi Zhang, Zhaoming Li

Abstract read
In one paragraph

Article in BMC medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Frontiers in microbiology · 2026
    Article
  10. Review
  11. Article
  12. Article
  13. 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

8 authors.

Zhuangzhuang ShiDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, Henan, China. zhuangzhuang_shi@126.com.
Wenxing JiangDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, Henan, China.
Hongwen LiLymphoma Diagnosis and Treatment Centre of Henan Province, Zhengzhou, 450052, Henan, China.
Yue ZhangDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, Henan, China.
Weili XueDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, Henan, China.
Yingjun WangDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, Henan, China.
Mingzhi ZhangDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, Henan, China. mingzhi_zhang1@163.com.
Zhaoming LiDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, Henan, China. fcclizm@zzu.edu.cn.

Funding

Funding for Scientific Research and Innovation Team of The First Affiliated Hospital of Zhengzhou University QNCXTD2023012Henan Province Youth Health Science and Technology Innovation Project LJRC2023014Joint Construction Project of Medical Science and Technology of Henan Province LHGJ20220386National Natural Science Foundation of China 82070209National Natural Science Foundation of China 82170183National Natural Science Foundation of China 82200206Natural Science Foundation of Henan Province 242300421019
6 · The paper itself

Abstract

backgroundNatural killer/T-cell lymphoma (NKTCL) is a highly aggressive subtype of lymphoma characterized by a poor prognosis. While immune checkpoint blockade (ICB) therapy has emerged as an effective treatment modality for various cancers, its efficacy among individuals is inconsistent and remains suboptimal for the majority of NKTCL patients. Faecalibacterium prausnitzii, recognized as a next-generation probiotic with immunomodulatory capabilities, has not yet been fully explored for its potential to influence the outcomes of ICB therapy.

methodsWe established syngeneic tumor-bearing mouse models of NKTCL and treated the mice with an anti-PD-L1 monoclonal antibody (mAb) and F. prausnitzii. Metabolomics analysis was performed to quantify butyrate concentrations in fecal, plasma, and tumor samples from the mice. Furthermore, we used flow cytometry, multiplex immunohistochemistry, and enzyme-linked immunosorbent assays to assess the effects of butyrate supplementation on antitumor immune responses in mice receiving anti-PD-L1 therapy. Additionally, an antibiotic-pretreated mouse model was utilized to further investigate the influence of F. prausnitzii on the efficacy of ICB therapy.

resultsThe combination of F. prausnitzii and an anti-PD-L1 mAb effectively inhibited tumor growth, primarily through the action of its metabolite butyrate. Notably, F. prausnitzii-derived butyrate played a crucial role in enhancing the efficacy of ICB therapy by augmenting antitumor immune responses, as evidenced by reduced PD-L1 expression and increased levels of cytotoxic CD8+ T cells within the tumor microenvironment. Moreover, prior administration of antibiotics significantly compromised the efficacy of the anti-PD-L1 mAb. However, supplementation with F. prausnitzii mitigated the negative effects of antibiotics and restored the altered gut microbiota in tumor-bearing mice.

conclusionsThis study highlights the potential of F. prausnitzii in augmenting ICB therapy and presents a novel gut probiotic-centered therapeutic strategy for the treatment of NKTCL.

Indexed as

B7-H1 AntigenFaecalibacterium prausnitziiImmune Checkpoint InhibitorsLymphoma, T-CellProbioticsAnimalsAntibodies, MonoclonalButyratesCell Line, TumorDisease Models, AnimalFemaleGastrointestinal MicrobiomeMiceMice, Inbred C57BLAntibodies, MonoclonalB7-H1 AntigenButyratesImmune Checkpoint InhibitorsButyrateFaecalibacterium prausnitziiGut microbiotaImmunotherapyNatural killer/T-cell lymphoma

Identifiers

PMID40597177
PMCPMC12220487

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.