Evidence map›Paper›PMID 30774630›Full record

ReviewFrontiers in immunology2019

Dendritic Cell Regulation of Graft-Vs.-Host Disease: Immunostimulation and Tolerance.

Hongshuang Yu, Yuanyuan Tian, Ying Wang, Shin Mineishi, Yi Zhang

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.1field-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

37 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Graft-Versus-Host Disease Mouse Models: A Clinical-Translational Perspective.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  5. Article
  6. Article
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  9. Review
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  11. Review
  12. Review
  13. Article
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  15. Article
  16. Article
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  18. Article
  19. Cell therapies in the clinic.Bioengineering & translational medicine · 2021
    Review
  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

5 authors at 2 institutions in 1 country.

Hongshuang YuFels Institute for Cancer Research and Molecular Biology, Temple University, Philadelphia, PA, United States.
Yuanyuan TianFels Institute for Cancer Research and Molecular Biology, Temple University, Philadelphia, PA, United States.
Ying WangFels Institute for Cancer Research and Molecular Biology, Temple University, Philadelphia, PA, United States.
Shin MineishiDepartment of Medicine, Pennsylvania State University, Hershey, PA, United States.
Yi ZhangFels Institute for Cancer Research and Molecular Biology, Temple University, Philadelphia, PA, United States.
Temple University · USPennsylvania State University · US

Funding

Synthetic rescue of antigen-driven T cells and alloimmunityR01AI143256 · NIAID · TEMPLE UNIV OF THE COMMONWEALTH · PI SOBOLOFF, JONATHAN A, ZHANG, YI · 2019 to 2023
$2.9M
DOT1L, reconstitution of plasmacytoid dendritic cells and alloimmunityR01HL154757 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI ZHANG, YI · 2021 to 2024
$2.6M
Ezh2-mediated Epigenetic Effects and AlloimmunityR01HL127351 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI ZHANG, YI · 2016 to 2019
$2.4M
Delta-like ligand 4+ dendritic cells and induction of alloimmunityR01CA172106 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHANG, YI · 2013 to 2017
$1.6M
NCI NIH HHS R01 CA172106NHLBI NIH HHS R01 HL127351NHLBI NIH HHS R01 HL154757NIAID NIH HHS R01 AI143256
6 · The paper itself

Abstract

Graft-vs.-host disease (GVHD) remains a significant cause of morbidity and mortality after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Significant progresses have been made in defining the dichotomous role of dendritic cells (DCs) in the development of GVHD. Host-derived DCs are important to elicit allogeneic T cell responses, whereas certain donor-types of DCs derived from newly engrafted hematopoietic stem/progenitor cells (HSPCs) can amply this graft-vs.-host reaction. In contrast, some DCs also play non-redundant roles in mediating immune tolerance. They induce apoptotic deletion of host-reactive donor T cells while promoting expansion and function of regulatory T cells (Treg). Unfortunately, this tolerogenic effect of DCs is impaired during GVHD. Severe GVHD in patients subject to allo-HSCT is associated with significantly decreased number of circulating peripheral blood DCs during engraftment. Existing studies reveal that GVHD causes delayed reconstitution of donor DCs from engrafted HSPCs, impairs the antigen presentation function of newly generated DCs and reduces the capacity of DCs to regulate Treg. The present review will discuss the importance of DCs in alloimmunity and the mechanism underlying DC reconstitution after allo-HSCT.

Indexed as

AnimalsDendritic CellsGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansImmune ToleranceImmunizationT-Lymphocytesalloreactive T cellsdendritic cellsdiseasegraft-vs.-hostimmune toleranceimmunostimulationtranscription factors

Identifiers

PMID30774630
PMCPMC6367268
OpenAlexW2913313103

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.