Evidence map›Paper›PMID 25846718›Full record

ArticleBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2015

Essential Role of Interleukin-12/23p40 in the Development of Graft-versus-Host Disease in Mice.

Yongxia Wu, David Bastian, Steven Schutt, Hung Nguyen, Jianing Fu, Jessica Heinrichs, Changqing Xia, Xue-Zhong Yu

Abstract read
In one paragraph

Article in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 27 citations in OpenAlex.

  1. Haematologica · 2018
    Trial
  2. Article
  3. MAIT cells and their implication in human oral diseases.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Cells · 2019
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. IL-17A ≠ Th17 in GvHD.Cellular & molecular immunology · 2018
    Article
  14. Article
  15. Article
  16. Review
  17. [Advances in the pathogenesis of chronic graft versus host disease].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2017
    Article
  18. Alarmins and Their Receptors as Modulators and Indicators of Alloimmune Responses.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2017
    Review
  19. Targeting Cytokines in GVHD Therapy.Journal of immunology research and therapy · 2017
    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

8 authors at 2 institutions in 2 countries.

Yongxia WuDepartment of Hematology, Xuanwu Hospital, Capital Medical University, Beijing, China; Department of Microbiology and Immunology, Medical University of South Carolina, Charleston, South Carolina.
David BastianDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, South Carolina.
Steven SchuttDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, South Carolina.
Hung NguyenDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, South Carolina.
Jianing FuDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, South Carolina.
Jessica HeinrichsDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, South Carolina.
Changqing XiaDepartment of Hematology, Xuanwu Hospital, Capital Medical University, Beijing, China; Pathology, Immunology and Laboratory Medicine, University of Florida, Gainesville, Florida.
Xue-Zhong YuDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, South Carolina; Department of Medicine, Medical University of South Carolina, Charleston, South Carolina. Electronic address: yux@musc.edu.
Medical University of South Carolina · USCapital Medical University · CN

Funding

Effects of Foxp3-Induced Regulatory T Cells on GVHD and GVT ActivityR01CA118116 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI YU, XUE-ZHONG · 2006 to 2015
$2.2M
Targeting IL-12/23 p40 Pathways for the Control of GVHDR01CA169116 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI YU, XUE-ZHONG · 2013 to 2017
$1.6M
Th1/Th17 Cell Differentiation in GVHD and GVLR01CA143812 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI YU, XUE-ZHONG · 2010 to 2013
$1.3M
Influence of Sex Steroids on HIV-1 Chemokine Coreceptor Expression in WomenK08AI080285 · NIAID · UNIVERSITY OF COLORADO DENVER · PI MEDITZ, AMIE L · 2009 to 2013
$661k
NCI NIH HHS CA118116NCI NIH HHS CA143812NCI NIH HHS CA169116NCI NIH HHS R01 CA118116NCI NIH HHS R01 CA143812NCI NIH HHS R01 CA169116NIAID NIH HHS K08 AI080285NIAID NIH HHS R01 AI080285
6 · The paper itself

Abstract

Graft-versus-host disease (GVHD), in both its acute (aGVHD) and chronic (cGVHD) forms, remains a major obstacle impeding successful allogeneic hematopoietic stem cell transplantation (allo-HSCT). T cells, in particular pathogenic T helper (Th) 1 and Th17 subsets, are a driving force for the induction of GVHD. IL-12 and IL-23 cytokines share a common p40 subunit and play a critical role in driving Th1 differentiation and in stabilizing the Th17 phenotype, respectively. In our current study, we hypothesized that p40 is an essential cytokine in the development of GVHD. By using p40-deficient mice, we found that both donor- and host-derived p40 contribute to the development of aGVHD. Neutralization of p40 with an anti-p40 mAb inhibited Th1- and Th17-polarization in vitro. Furthermore, anti-p40 treatment reduced aGVHD severity while preserving the graft-versus-leukemia (GVL) activity. Alleviation of aGVHD was associated with an increase of Th2 differentiation and a decrease of Th1 and Th17 effector T cells in the GVHD target organs. In addition, anti-p40 treatment attenuated the severity of sclerodermatous cGVHD. These results provide a strong rationale that blockade of p40 may represent a promising therapeutic strategy in preventing and treating aGVHD and cGVHD while sparing the GVL effect after allo-HSCT.

Indexed as

AnimalsAntibodies, NeutralizingBone Marrow TransplantationCell DifferentiationDisease Models, AnimalGene ExpressionGraft vs Host DiseaseGraft vs Leukemia EffectHistocompatibility TestingHumansInterleukin-12 Subunit p40Leukemia, Myeloid, AcuteLymphocyte DepletionLymphoma, B-CellMiceMice, Inbred C57BLAntibodies, NeutralizingInterleukin-12 Subunit p40Antigen-presenting cellsGraft-versus-host diseaseIL-12IL-23p40T cell differentiationT cell migrationT cells

Identifiers

PMID25846718
PMCPMC4466028
OpenAlexW2112175073

What OpenQuestion holds

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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.