Evidence map›Paper›PMID 26809474›Full record

ArticleeLife2016

MHC-compatible bone marrow stromal/stem cells trigger fibrosis by activating host T cells in a scleroderma mouse model.

Yoko Ogawa, Satoru Morikawa, Hideyuki Okano, Yo Mabuchi, Sadafumi Suzuki, Tomonori Yaguchi, Yukio Sato, Shin Mukai, Saori Yaguchi, Takaaki Inaba and 5 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Stem cell therapy in systemic sclerosis.Clinical rheumatology · 2025
    Review
  4. Observational
  5. Article
  6. Article
  7. A Novel Murine Model for Lupus-Like Ocular Chronic Graft-Versus-Host Disease.Investigative ophthalmology & visual science · 2024
    Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
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 at 2 institutions in 1 country.

Yoko OgawaDepartment of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.
Satoru MorikawaDepartment of Dentistry and Oral Surgery, Keio University School of Medicine, Tokyo, Japan.
Hideyuki OkanoDepartment of Physiology, Keio University School of Medicine, Tokyo, Japan.
Yo MabuchiDepartment of Physiology, Keio University School of Medicine, Tokyo, Japan.
Sadafumi SuzukiDepartment of Physiology, Keio University School of Medicine, Tokyo, Japan.
Tomonori YaguchiDivision of Cellular Signaling, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo, Japan.
Yukio SatoDepartment of Physiology, Keio University School of Medicine, Tokyo, Japan.
Shin MukaiDepartment of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.
Saori YaguchiDepartment of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.
Takaaki InabaDepartment of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.
Shinichiro OkamotoDivision of Hematology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
Yutaka KawakamiDivision of Cellular Signaling, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo, Japan.
Kazuo TsubotaDepartment of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.
Yumi MatsuzakiDepartment of Life Science Laboratory of Tumor Biology, Faculty of Medicine, Shimane University, Izumo, Japan.
Shigeto ShimmuraDepartment of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.
Keio University · JPShimane University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibrosis of organs is observed in systemic autoimmune disease. Using a scleroderma mouse, we show that transplantation of MHC compatible, minor antigen mismatched bone marrow stromal/stem cells (BMSCs) play a role in the pathogenesis of fibrosis. Removal of donor BMSCs rescued mice from disease. Freshly isolated PDGFRα(+) Sca-1(+) BMSCs expressed MHC class II following transplantation and activated host T cells. A decrease in FOXP3(+) CD25(+) Treg population was observed. T cells proliferated and secreted IL-6 when stimulated with mismatched BMSCs in vitro. Donor T cells were not involved in fibrosis because transplanting T cell-deficient RAG2 knock out mice bone marrow still caused disease. Once initially triggered by mismatched BMSCs, the autoimmune phenotype was not donor BMSC dependent as the phenotype was observed after effector T cells were adoptively transferred into naïve syngeneic mice. Our data suggest that minor antigen mismatched BMSCs trigger systemic fibrosis in this autoimmune scleroderma model.

Indexed as

AnimalsBone MarrowBone Marrow TransplantationDisease Models, AnimalFibrosisMiceScleroderma, DiffuseStem CellsStromal CellsT-Lymphocytesadoptive transferautoimmune response/diseaseauto-reactive T cellsdevelopmental biologydry eye diseasefibrosisimmunologymesenchymal stem cellsmousestem cells

Identifiers

PMID26809474
PMCPMC4739756
OpenAlexW2277221157

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.