Evidence map›Paper›PMID 39078050›Full record

ArticleGut microbes

MS-20 enhances the gut microbiota-associated antitumor effects of anti-PD1 antibody.

Pei-Jung Lee, Chien-Min Hung, Ai-Jen Yang, Cheng-Yu Hou, Hung-Wen Chou, Yi-Chung Chang, Wen-Cheng Chu, Wen-Yen Huang, Wen-Chih Kuo, Chia-Chun Yang and 9 more

Abstract read
In one paragraph

Article in Gut microbes. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. [Fecal Microbiota Transplantation: A Promising Avenue for Lung Cancer Therapy].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2025
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  11. Metabolic Checkpoints in CD8International journal of biological sciences · 2026
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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

19 authors.

Pei-Jung LeePharmaceutical Research & Development, Microbio Co, Ltd, Taipei, Taiwan.
Chien-Min HungPharmaceutical Research & Development, Microbio Co, Ltd, Taipei, Taiwan.
Ai-Jen YangPharmaceutical Research & Development, Microbio Co, Ltd, Taipei, Taiwan.
Cheng-Yu HouPharmaceutical Research & Development, Microbio Co, Ltd, Taipei, Taiwan.
Hung-Wen ChouAnimal Center for Drug Screening, Oneness Biotech Co, Ltd, Taipei, Taiwan.
Yi-Chung ChangNucleic Acid Drug Division, Microbio (Shanghai) Biotech Company, Shanghai, China.
Wen-Cheng ChuPharmaceutical Research & Development, Microbio Co, Ltd, Taipei, Taiwan.
Wen-Yen HuangPharmaceutical Research & Development, Microbio Co, Ltd, Taipei, Taiwan.
Wen-Chih KuoPharmaceutical Research & Development, Microbio Co, Ltd, Taipei, Taiwan.
Chia-Chun YangNucleic Acid Drug Division, Microbio (Shanghai) Biotech Company, Shanghai, China.
Kuo-I LinGenomics Research Center, Academia Sinica, Taipei, Taiwan.
Kuo-Hsuan HungGenomics Research Center, Academia Sinica, Taipei, Taiwan.
Li-Chun ChangDivision of Gastroenterology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Kang-Yun LeeDivision of Pulmonary Medicine, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan.
Han-Pin KuoPulmonary Medicine Research Center, Taipei Medical University, Taipei, Taiwan.
Kung-Ming LuGeneral manager's office, Microbio Co., Ltd., Taipei, Taiwan.
Hsin-Chih LaiGeneral manager's office, Revivebio Co, Ltd, Taipei, Taiwan.ORCID 0000-0002-0605-5040
Ming-Liang KuoGeneral manager's office, Microbio Co., Ltd., Taipei, Taiwan.
Wan-Jiun ChenPharmaceutical Research & Development, Microbio Co, Ltd, Taipei, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer immunotherapy has been regarded as a promising strategy for cancer therapy by blocking immune checkpoints and evoking immunity to fight cancer, but its efficacy seems to be heterogeneous among patients. Manipulating the gut microbiota is a potential strategy for enhancing the efficacy of immunotherapy. Here, we report that MS-20, also known as "Symbiota®", a postbiotic that comprises abundant microbial metabolites generated from a soybean-based medium fermented with multiple strains of probiotics and yeast, inhibited colon and lung cancer growth in combination with an anti-programmed cell death 1 (PD1) antibody in xenograft mouse models. Mechanistically, MS-20 remodeled the immunological tumor microenvironment by increasing effector CD8

Indexed as

CD8-Positive T-LymphocytesGastrointestinal MicrobiomeProgrammed Cell Death 1 ReceptorTumor MicroenvironmentAnimalsCell Line, TumorColonic NeoplasmsFecal Microbiota TransplantationFemaleHumansImmune Checkpoint InhibitorsImmunotherapyLung NeoplasmsMiceMice, Inbred BALB CProbioticsImmune Checkpoint InhibitorsProgrammed Cell Death 1 Receptorcancer immunotherapycolorectal cancerGut microbiota

Identifiers

PMID39078050
PMCPMC11290773

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Registered trials

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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.