Evidence map›Paper›PMID 39798567›Full record

ArticleCell reports. Medicine2025

Intestinal Akkermansia muciniphila complements the efficacy of PD1 therapy in MAFLD-related hepatocellular carcinoma.

Xue Qian Wu, Fan Ying, Katherine Po Sin Chung, Carmen Oi Ning Leung, Rainbow Wing Hei Leung, Karl Kam Hei So, Martina Mang Leng Lei, Wing Ki Chau, Man Tong, Jun Yu and 5 more

Abstract read
In one paragraph

Article in Cell reports. Medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 3 pooled it
–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

51 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
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  4. Article
  5. Translational cancer research · 2026
    Article
  6. Journal for immunotherapy of cancer · 2026
    Article
  7. Review
  8. Article
  9. Emerging Immune-Based Therapeutic Strategies in Hepatocellular Carcinoma.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Review
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  11. Article
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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

15 authors.

Xue Qian WuDepartment of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong SAR, China.
Fan YingDepartment of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong SAR, China.
Katherine Po Sin ChungDepartment of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong SAR, China.
Carmen Oi Ning LeungDepartment of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong SAR, China.
Rainbow Wing Hei LeungDepartment of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong SAR, China.
Karl Kam Hei SoSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China.
Martina Mang Leng LeiDepartment of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong SAR, China.
Wing Ki ChauDepartment of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong SAR, China.
Man TongSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China.
Jun YuInstitute of Digestive Disease and Department of Medicine and Therapeutics, State Key Laboratory of Digestive Disease, Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China.
Dai WeiDepartment of Clinical Oncology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
William Chi Shing TaiDepartment of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong SAR, China.
Stephanie MaSchool of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China; State Key Laboratory of Liver Research, The University of Hong Kong, Hong Kong SAR, China.
Yin Ying LuComprehensive Liver Cancer Center, The Fifth Medical Center of PLA General Hospital, Beijing, China. Electronic address: luyinying1973@163.com.
Terence Kin Wah LeeDepartment of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong SAR, China; State Key Laboratory of Chemical Biology and Drug Discovery, The Hong Kong Polytechnic University, Hong Kong SAR, China; Research Institute for Future Food, The Hong Kong Polytechnic University, Hong Kong SAR, China. Electronic address: terence.kw.lee@polyu.edu.hk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint inhibitors are not effective for metabolic dysfunction-associated fatty liver disease (MAFLD)-hepatocellular carcinoma (HCC) patients, and identifying the key gut microbiota that contributes to immune resistance in these patients is crucial. Analysis using 16S rRNA sequencing reveals a decrease in Akkermansia muciniphila (Akk) during MAFLD-promoted HCC development. Administration of Akk ameliorates liver steatosis and effectively attenuates the tumor growth in orthotopic MAFLD-HCC mouse models. Akk repairs the intestinal lining, with a decrease in the serum lipopolysaccharide (LPS) and bile acid metabolites, along with decrease in the populations of monocytic myeloid-derived suppressor cells (m-MDSCs) and M2 macrophages. Akk in combination with PD1 treatment exerts maximal growth-suppressive effect in multiple MAFLD-HCC mouse models with increased infiltration and activation of T cells. Clinically, low Akk levels are correlated with PD1 resistance and poor progression-free survival. In conclusion, Akk is involved in the immune resistance of MAFLD-HCC and serves as a predictive biomarker for PD1 response in HCC.

Indexed as

AkkermansiaCarcinoma, HepatocellularLiver NeoplasmsProgrammed Cell Death 1 ReceptorAnimalsDisease Models, AnimalGastrointestinal MicrobiomeHumansImmune Checkpoint InhibitorsMaleMiceMice, Inbred C57BLImmune Checkpoint InhibitorsProgrammed Cell Death 1 ReceptorAkkermansia muciniphilagut microbiotaHCCimmune checkpoint therapiesMAFLD

Identifiers

PMID39798567
PMCPMC11866522

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.