Evidence map›Paper›PMID 25119573›Full record

ArticlePloS one2014

Dysfunction of bone marrow vascular niche in acute graft-versus-host disease after MHC-haploidentical bone marrow transplantation.

Yonghua Yao, Xianmin Song, Hui Cheng, Gusheng Tang, Xiaoxia Hu, Hong Zhou, Jianmin Wang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 39 citations in OpenAlex.

  1. Trial
  2. Deep insight into cytokine storm: from pathogenesis to treatment.Signal transduction and targeted therapy · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Adipose tissue-derived stem cells modulate immune functionExperimental and therapeutic medicine · 2020
    Article
  9. Inhibition of 5-lipoxygenase alleviates graft-versus-host disease.The Journal of experimental medicine · 2017
    Article
  10. Article
  11. Review
  12. 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

7 authors at 2 institutions in 1 country.

Yonghua YaoDepartment of Hematology, Institute of Hematology, Changhai Hospital, Shanghai, China.
Xianmin SongDepartment of Hematology, Institute of Hematology, Changhai Hospital, Shanghai, China.
Hui ChengDepartment of Hematology, Institute of Hematology, Changhai Hospital, Shanghai, China.
Gusheng TangDepartment of Hematology, Institute of Hematology, Changhai Hospital, Shanghai, China.
Xiaoxia HuDepartment of Hematology, Institute of Hematology, Changhai Hospital, Shanghai, China.
Hong ZhouDepartment of Hematology, Institute of Hematology, Changhai Hospital, Shanghai, China.
Jianmin WangDepartment of Hematology, Institute of Hematology, Changhai Hospital, Shanghai, China.
Changhai Hospital · CNSecond Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute graft-versus-host disease (aGvHD) is the most common complication of allogeneic hematopoietic stem cell transplantation (HSCT), which is often accompanied by impaired hematopoietic reconstitution. Sinusoidal endothelial cells (SECs) constitute bone marrow (BM) vascular niche that plays an important role in supporting self-renewal capacity and maintaining the stability of HSC pool. Here we provide evidences that vascular niche is a target of aGvHD in a major histocompatibility complex (MHC)-haploidentical matched murine HSCT model. The results demonstrated that hematopoietic cells derived from GvHD mice had the capacity to reconstitute hematopoiesis in healthy recipient mice. However, hematopoietic cells from healthy donor mice failed to reconstitute hematopoiesis in GvHD recipient mice, indicating that the BM niche was impaired by aGvHD in this model. We further demonstrated that SECs were markedly reduced in the BM of aGvHD mice. High level of Fas and caspase-3 expression and high rate of apoptosis were identified in SECs, indicating that SECs were destroyed by aGvHD in this murine HSCT model. Furthermore, high Fas ligand expression on engrafted donor CD4(+), but not CD8(+) T cells, and high level MHC-II but not MHC-I expression on SECs, suggested that SECs apoptosis was mediated by CD4(+) donor T cells through the Fas/FasL pathway.

Indexed as

AnimalsBone Marrow TransplantationCaspase 3CD4-Positive T-LymphocytesEndothelial CellsEnzyme-Linked Immunosorbent Assayfas ReceptorFlow CytometryGraft vs Host DiseaseHematopoiesisHematopoietic Stem CellsImmunohistochemistryKaplan-Meier EstimateMajor Histocompatibility ComplexMiceReal-Time Polymerase Chain ReactionCaspase 3Fas protein, mousefas Receptor

Identifiers

PMID25119573
PMCPMC4131885
OpenAlexW2024999693

What OpenQuestion holds

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LicenceCC BY
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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.