Evidence map›Paper›PMID 26012567›Full record

ArticleBlood2015

Blocking TWEAK-Fn14 interaction inhibits hematopoietic stem cell transplantation-induced intestinal cell death and reduces GVHD.

Martin Chopra, Andreas Brandl, Daniela Siegmund, Anja Mottok, Viktoria Schäfer, Marlene Biehl, Sabrina Kraus, Carina A Bäuerlein, Miriam Ritz, Katharina Mattenheimer and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

23 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Fn14 and TNFR2 as regulators of cytotoxic TNFR1 signaling.Frontiers in cell and developmental biology · 2023
    Review
  5. Review
  6. Article
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  8. Article
  9. Article
  10. Article
  11. Review
  12. CD150American journal of translational research · 2019
    Article
  13. Article
  14. Frontiers in pharmacology · 2018
    Article
  15. Review
  16. Targeting Cytokines in GVHD Therapy.Journal of immunology research and therapy · 2017
    Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 3 institutions in 1 country.

Martin ChopraDepartment of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany; Center for Interdisciplinary Clinical Research, University of Würzburg, Würzburg, Germany;
Andreas BrandlDepartment of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany; Center for Interdisciplinary Clinical Research, University of Würzburg, Würzburg, Germany;
Daniela SiegmundDivision of Molecular Internal Medicine, Department of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany;
Anja MottokInstitute of Pathology, University of Würzburg and Comprehensive Cancer Center Mainfranken, Würzburg, Germany;
Viktoria SchäferDivision of Molecular Internal Medicine, Department of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany;
Marlene BiehlDepartment of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany; Center for Interdisciplinary Clinical Research, University of Würzburg, Würzburg, Germany;
Sabrina KrausDepartment of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany; Center for Interdisciplinary Clinical Research, University of Würzburg, Würzburg, Germany; Else-Kröner-Forschungskolleg Würzburg, Würzburg, Germany;
Carina A BäuerleinDepartment of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany; Center for Interdisciplinary Clinical Research, University of Würzburg, Würzburg, Germany;
Miriam RitzDepartment of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany; Center for Interdisciplinary Clinical Research, University of Würzburg, Würzburg, Germany;
Katharina MattenheimerDepartment of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany; Center for Interdisciplinary Clinical Research, University of Würzburg, Würzburg, Germany;
Stefanie SchwinnDepartment of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany; Center for Interdisciplinary Clinical Research, University of Würzburg, Würzburg, Germany;
Axel SeherDepartment of Oral and Maxillofacial Plastic Surgery, University Hospital Würzburg, Würzburg, Germany; and.
Thomas GrabingerDepartment of Biology, University of Konstanz, Konstanz, Germany.
Hermann EinseleDepartment of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany;
Andreas RosenwaldInstitute of Pathology, University of Würzburg and Comprehensive Cancer Center Mainfranken, Würzburg, Germany;
Thomas BrunnerDepartment of Biology, University of Konstanz, Konstanz, Germany.
Andreas BeilhackDepartment of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany; Center for Interdisciplinary Clinical Research, University of Würzburg, Würzburg, Germany; Else-Kröner-Forschungskolleg Würzburg, Würzburg, Germany;
Harald WajantDivision of Molecular Internal Medicine, Department of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany;
Universitätsklinikum Würzburg · DEUniversity of Würzburg · DEUniversity of Konstanz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inhibition of the tumor necrosis factor (TNF)-like weak inducer of apoptosis (TWEAK)/fibroblast growth factor-inducible 14 (Fn14) system reduces intestinal cell death and disease development in several models of colitis. In view of the crucial role of TNF and intestinal cell death in graft-versus-host disease (GVHD) and the ability of TWEAK to enhance TNF-induced cell death, we tested here the therapeutic potential of Fn14 blockade on allogeneic hematopoietic cell transplantation (allo-HCT)-induced intestinal GVHD. An Fn14-specific blocking human immunoglobulin G1 antibody variant with compromised antibody-dependent cellular cytotoxicity (ADCC) activity strongly inhibited the severity of murine allo-HCT-induced GVHD. Treatment of the allo-HCT recipients with this monoclonal antibody reduced cell death of gastrointestinal cells but neither affected organ infiltration by donor T cells nor cytokine production. Fn14 blockade also inhibited intestinal cell death in mice challenged with TNF. This suggests that the protective effect of Fn14 blockade in allo-HCT is based on the protection of intestinal cells from TNF-induced apoptosis and not due to immune suppression. Importantly, Fn14 blockade showed no negative effect on graft-versus-leukemia/lymphoma (GVL) activity. Thus, ADCC-defective Fn14-blocking antibodies are not only possible novel GVL effect-sparing therapeutics for the treatment of GVHD but might also be useful for the treatment of other inflammatory bowel diseases where TNF-induced cell death is of relevance.

Indexed as

ApoptosisTumor Necrosis Factor InhibitorsAnimalsAntibodies, Monoclonal, Murine-DerivedAntibody-Dependent Cell CytotoxicityBlotting, WesternCells, CulturedCytokine TWEAKDisease Models, AnimalFemaleFluorescent Antibody TechniqueGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansImmunoglobulin GIntestinal MucosaAntibodies, Monoclonal, Murine-DerivedCytokine TWEAKFcgr1 protein, mouseImmunoglobulin GReceptors, IgGReceptors, Tumor Necrosis FactorRituximabRNA, MessengerTNFRSF12A protein, humanTnfrsf12a protein, mouseTnfsf12 protein, mouseTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsTumor Necrosis FactorsTWEAK Receptor

Identifiers

PMID26012567
PMCPMC4536890
OpenAlexW1488403761

What OpenQuestion holds

Textmetadata
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.