Evidence map›Paper›PMID 35180303›Full record

ArticleCancer discovery2022

Dietary Lactobacillus-Derived Exopolysaccharide Enhances Immune-Checkpoint Blockade Therapy.

Hirotaka Kawanabe-Matsuda, Kazuyoshi Takeda, Marie Nakamura, Seiya Makino, Takahiro Karasaki, Kazuhiro Kakimi, Megumi Nishimukai, Tatsukuni Ohno, Jumpei Omi, Kuniyuki Kano and 7 more

Open access · greenAbstract read
In one paragraph

Article in Cancer discovery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed, 1 pooled it
11.2field-weighted citation impact, top 1% of its field
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

94 citing papers in PubMed, 1 synthesis or guideline pooled it, 136 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. Review

34 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 9 institutions in 4 countries.

Hirotaka Kawanabe-MatsudaDepartment of Biofunctional Microbiota, Graduate School of Medicine, Juntendo University, Tokyo, Japan.ORCID 0000-0001-5432-3807
Kazuyoshi TakedaDepartment of Biofunctional Microbiota, Graduate School of Medicine, Juntendo University, Tokyo, Japan.ORCID 0000-0002-5539-310X
Marie NakamuraResearch Team, Co-Creation Center, Meiji Holdings Co., Ltd., Hachioji, Japan.
Seiya MakinoDepartment of Biofunctional Microbiota, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Takahiro KarasakiDepartment of Immunotherapeutics, The University of Tokyo Hospital, Tokyo, Japan.ORCID 0000-0001-6863-2360
Kazuhiro KakimiDepartment of Immunotherapeutics, The University of Tokyo Hospital, Tokyo, Japan.ORCID 0000-0003-2631-3040
Megumi NishimukaiDepartment of Animal Science, Faculty of Agriculture, Iwate University, Morioka, Japan.ORCID 0000-0001-6545-2436
Tatsukuni OhnoDepartment of Biofunctional Microbiota, Graduate School of Medicine, Juntendo University, Tokyo, Japan.ORCID 0000-0002-9331-082X
Jumpei OmiDepartment of Health Chemistry, Graduate School of Pharmaceutical Science, The University of Tokyo, Tokyo, Japan.
Kuniyuki KanoDepartment of Health Chemistry, Graduate School of Pharmaceutical Science, The University of Tokyo, Tokyo, Japan.ORCID 0000-0002-4539-5750
Akiharu UwamizuDepartment of Health Chemistry, Graduate School of Pharmaceutical Science, The University of Tokyo, Tokyo, Japan.ORCID 0000-0003-3300-7324
Hideo YagitaDepartment of Immunology, School of Medicine, Juntendo University, Tokyo, Japan.
Ivo Gomperts BonecaInstitut Pasteur, Unit of Biology and Genetics of Bacterial Cell Wall, Paris, France. INSERM, Équipe Avenir, Paris, France.ORCID 0000-0001-8122-509X
Gérard EberlMicroenvironment and Immunity Unit, Institut Pasteur, Paris, France.
Junken AokiDepartment of Health Chemistry, Graduate School of Pharmaceutical Science, The University of Tokyo, Tokyo, Japan.ORCID 0000-0001-9435-1896
Mark J SmythImmunology in Cancer and Infection Laboratory, QIMR Berghofer Medical Research Institute, Herston, Queensland, Australia.
Ko OkumuraDepartment of Biofunctional Microbiota, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Juntendo University · JPTohoku University · JPUniversity of Tokyo Hospital · JPInserm · FRInstitut Pasteur · FRIwate University · JPOji Holdings (Japan) · JPQIMR Berghofer Medical Research Institute · AUTokyo Dental College · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microbes and their byproducts have been reported to regulate host health and immune functions. Here we demonstrated that microbial exopolysaccharide produced by Lactobacillus delbrueckii subsp. bulgaricus OLL1073R-1 (EPS-R1) induced CCR6+ CD8+ T cells of mice and humans. In mice, ingestion of EPS-R1 augmented antitumor effects of anti-CTLA-4 or anti-PD-1 monoclonal antibody against CCL20-expressing tumors, in which infiltrating CCR6+ CD8+ T cells were increased and produced IFNγ accompanied by a substantial immune response gene expression signature maintaining T-cell functions. Of note, the antitumor adjuvant effect of EPS-R1 was also observed in germ-free mice. Furthermore, the induction of CCR6 expression was mediated through the phosphorylated structure in EPS-R1 and a lysophosphatidic acid receptor on CD8+ T cells. Overall, we find that dietary EPS-R1 consumption induces CCR6+ CD8+ T cells in Peyer's patches, favoring a tumor microenvironment that augments the therapeutic effect of immune-checkpoint blockade depending on CCL20 production by tumors. SIGNIFICANCE: Gut microbiota- and probiotic-derived metabolites are attractive agents to augment the efficacy of immunotherapies. Here we demonstrated that dietary consumption of Lactobacillus-derived exopolysaccharide induced CCR6+ CD8+ T cells in Peyer's patches and improved the tumor microenvironment to augment the therapeutic effects of immune-checkpoint blockade against CCL20-producing tumors. See related commentary by Di Luccia and Colonna, p. 1189. This article is highlighted in the In This Issue feature, p. 1171.

Indexed as

LactobacillusNeoplasmsCD8-Positive T-LymphocytesHumansImmune Checkpoint InhibitorsTumor MicroenvironmentImmune Checkpoint Inhibitors

Identifiers

PMID35180303
PMCPMC9662940
OpenAlexW4212790658

What Socratic 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 Socratic graph.