Evidence map›Paper›PMID 39693612›Full record

ArticleBlood2025

Oral inflammation and microbiome dysbiosis exacerbate chronic graft-versus-host disease.

Yui Kambara, Hideaki Fujiwara, Akira Yamamoto, Kazuyoshi Gotoh, Shuma Tsuji, Mari Kunihiro, Tadashi Oyama, Toshiki Terao, Ayame Sato, Takehiro Tanaka and 11 more

Abstract read
In one paragraph

Article in Blood, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Feasibility of tooth brushing during prolonged neutropenia in adults receiving intensive induction for acute leukemia: a randomized trial.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Trial
  2. Trial
  3. Article
  4. Chronic graft-versus-host disease.Nature reviews. Disease primers · 2026
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors.

Yui KambaraDepartment of Hematology, Oncology and Respiratory Medicine, Okayama University Medical School, Okayama, Japan.ORCID 0000-0002-1968-0654
Hideaki FujiwaraDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.ORCID 0000-0002-0734-9315
Akira YamamotoDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.ORCID 0000-0001-7574-6446
Kazuyoshi GotohDepartment of Medical Laboratory Science, Okayama University Graduate School of Health Sciences, Okayama, Japan.
Shuma TsujiDepartment of Microbiology and Genetics, Okayama University Graduate School of Health Sciences, Okayama, Japan.
Mari KunihiroDepartment of Hematology, Oncology and Respiratory Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Tadashi OyamaDepartment of Hematology, Oncology and Respiratory Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.ORCID 0009-0005-6393-5027
Toshiki TeraoDepartment of Hematology, Oncology and Respiratory Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.ORCID 0000-0002-6728-3346
Ayame SatoDivision of Hospital Dentistry, Okayama University Hospital, Okayama, Japan.
Takehiro TanakaDepartment of Pathology and Oncology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Daniel PeltierDivision of Pediatric Hematology, Oncology, and Stem Cell Transplantation, Department of Pediatrics, Herman B Wells Center for Pediatric Research, Simon Cancer Center, Indiana University School of Medicine, Indianapolis, IN.ORCID 0000-0001-6069-9894
Keisuke SeikeDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Hisakazu NishimoriDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Noboru AsadaDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.ORCID 0000-0001-7322-5460
Daisuke EnnishiCenter for Comprehensive Genomic Medicine, Okayama University Hospital, Okayama, Japan.
Keiko FujiiDepartment of Clinical Laboratory, Okayama University Hospital, Okayama, Japan.ORCID 0009-0005-7614-2448
Nobuharu FujiiDivision of Blood Transfusion, Okayama University Hospital, Okayama, Japan.ORCID 0000-0002-8043-7768
Ken-Ichi MatsuokaDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.ORCID 0000-0001-7955-8266
Yoshihiko SogaDivision of Hospital Dentistry, Okayama University Hospital, Okayama, Japan.ORCID 0000-0001-5346-1474
Pavan ReddyDan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX.
Yoshinobu MaedaDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.ORCID 0000-0003-1634-5487

Funding

Long noncoding RNA-mediated regulation of T-cell alloimmunityK08HL157619 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Daniel C. Peltier · 2022 to 2026
$646k
NHLBI NIH HHS K08 HL157619
6 · The paper itself

Abstract

abstractThe oral microbiota, second in abundance to the gut, is implicated in chronic systemic diseases, but its specific role in graft-versus-host disease (GVHD) pathogenesis has been unclear. Our study finds that mucositis-induced oral dysbiosis in patients after hematopoietic cell transplantation (HCT) associated with increased chronic GVHD (cGVHD), even in patients receiving posttransplant cyclophosphamide. In murine HCT models, oral dysbiosis caused by bilateral molar ligatures exacerbated cGVHD and increased bacterial load in the oral cavity and gut, with Enterococcaceae significantly increasing in both organs. In this model, the migration of Enterococcaceae to cervical lymph nodes both before and after transplantation activated antigen-presenting cells, thereby promoting the expansion of donor-derived inflammatory T cells. Based on these results, we hypothesize that pathogenic bacteria increase in the oral cavity might not only exacerbate local inflammation but also enhance systemic inflammation throughout the HCT course. Additionally, these bacteria translocated to the gut and formed ectopic colonies, further amplifying systemic inflammation. Furthermore, interventions targeting the oral microbiome mitigated murine cGVHD. Collectively, our findings highlight the importance of oral dysbiosis in cGVHD and suggest that modulation of the oral microbiome during transplantation may be an effective approach for preventing or treating cGVHD.

Indexed as

DysbiosisGraft vs Host DiseaseHematopoietic Stem Cell TransplantationInflammationMicrobiotaMouthStomatitisAdultAnimalsChronic DiseaseFemaleGastrointestinal MicrobiomeHumansMaleMiceMice, Inbred C57BL

Identifiers

PMID39693612
PMCPMC11867138

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.