Evidence map›Paper›PMID 27980780›Full record

ArticleImmunity, inflammation and disease2016

Hsp90 inhibition ameliorates CD4

Carsten Berges, Thomas Kerkau, Sandra Werner, Nelli Wolf, Nadine Winter, Thomas Hünig, Hermann Einsele, Max S Topp, Niklas Beyersdorf

Open access · goldAbstract read
In one paragraph

Article in Immunity, inflammation and disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 92% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 2 institutions in 1 country.

Carsten BergesDepartment of Internal Medicine II Division of Hematology University Hospital Würzburg Würzburg Germany.
Thomas KerkauInstitute for Virology and Immunobiology University of Würzburg Würzburg Germany.
Sandra WernerInstitute for Virology and Immunobiology University of Würzburg Würzburg Germany.
Nelli WolfInstitute for Virology and Immunobiology University of Würzburg Würzburg Germany.
Nadine WinterDepartment of Internal Medicine II Division of Hematology University Hospital Würzburg Würzburg Germany.
Thomas HünigInstitute for Virology and Immunobiology University of Würzburg Würzburg Germany.
Hermann EinseleDepartment of Internal Medicine II Division of Hematology University Hospital Würzburg Würzburg Germany.
Max S ToppDepartment of Internal Medicine II Division of Hematology University Hospital Würzburg Würzburg Germany.
Niklas BeyersdorfInstitute for Virology and Immunobiology University of Würzburg Würzburg Germany.
University of Würzburg · DEUniversitätsklinikum Würzburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionFor many patients with leukemia only allogeneic bone marrow transplantion provides a chance of cure. Co-transplanted mature donor T cells mediate the desired Graft versus Tumor (GvT) effect required to destroy residual leukemic cells. The donor T cells very often, however, also attack healthy tissue of the patient inducing acute Graft versus Host Disease (aGvHD)-a potentially life-threatening complication.

methodsTherefore, we used the well established C57BL/6 into BALB/c mouse aGvHD model to evaluate whether pharmacological inhibition of heat shock protein 90 (Hsp90) would protect the mice from aGvHD.

resultsTreatment of the BALB/c recipient mice from day 0 to +2 after allogeneic CD4

conclusionsOur data, thus, suggest that Hsp90 inhibition might constitute a novel approach to reduce aGvHD in patients without abrogating the desired GvT effect.

Indexed as

CD4-Positive T-LymphocytesAnimalsBone Marrow TransplantationGraft vs Host DiseaseHSP90 Heat-Shock ProteinsHumansMiceMice, Inbred BALB CMice, Inbred C57BLHSP90 Heat-Shock ProteinsAcute graft‐versus‐host diseaseCD4+ T cellsgraft versus tumorheat shock protein 90hematopoietic stem cell transplantationregulatory T cells

Identifiers

PMID27980780
PMCPMC5134726
OpenAlexW2530798255

What OpenQuestion holds

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LicenceCC BY
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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.