Evidence map›Paper›PMID 29376889›Full record

ArticleThe Journal of clinical investigation2018

BATF-dependent IL-7RhiGM-CSF+ T cells control intestinal graft-versus-host disease.

Evelyn Ullrich, Benjamin Abendroth, Johanna Rothamer, Carina Huber, Maike Büttner-Herold, Vera Buchele, Tina Vogler, Thomas Longerich, Sebastian Zundler, Simon Völkl and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.8field-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

31 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
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  9. Novel T cell/organoid culture system allowsFrontiers in immunology · 2023
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  10. Review
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  14. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 7 institutions in 2 countries.

Evelyn UllrichDepartment of Medicine 5, University Hospital Erlangen, University of Erlangen-Nuremberg, Erlangen, Germany.
Benjamin AbendrothDepartment of Medicine 1, University Hospital Erlangen, University of Erlangen-Nuremberg, Kussmaul Campus for Medical Research, Erlangen, Germany.
Johanna RothamerDepartment of Medicine 5, University Hospital Erlangen, University of Erlangen-Nuremberg, Erlangen, Germany.
Carina HuberDepartment of Medicine 1, University Hospital Erlangen, University of Erlangen-Nuremberg, Kussmaul Campus for Medical Research, Erlangen, Germany.
Maike Büttner-HeroldInstitute of Pathology, Department of Nephropathology, University Hospital Erlangen, Erlangen, Germany.
Vera BucheleDepartment of Medicine 1, University Hospital Erlangen, University of Erlangen-Nuremberg, Kussmaul Campus for Medical Research, Erlangen, Germany.
Tina VoglerDepartment of Medicine 1, University Hospital Erlangen, University of Erlangen-Nuremberg, Kussmaul Campus for Medical Research, Erlangen, Germany.
Thomas LongerichInstitute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.
Sebastian ZundlerDepartment of Medicine 1, University Hospital Erlangen, University of Erlangen-Nuremberg, Kussmaul Campus for Medical Research, Erlangen, Germany.
Simon VölklDepartment of Medicine 5, University Hospital Erlangen, University of Erlangen-Nuremberg, Erlangen, Germany.
Andreas BeilhackCenter for Interdisciplinary Clinical Research, Würzburg University, Würzburg, Germany.
Stefan Rose-JohnInstitute of Biochemistry, Christian-Albrechts-University, Kiel, Germany.
Stefan WirtzDepartment of Medicine 1, University Hospital Erlangen, University of Erlangen-Nuremberg, Kussmaul Campus for Medical Research, Erlangen, Germany.
Georg F WeberDepartment of Surgery, University Hospital Erlangen, University of Erlangen-Nuremberg, Erlangen, Germany.
Sakhila GhimireDepartment of Hematology and Oncology, University Hospital Regensburg, Regensburg, Germany.
Marina KreutzDepartment of Hematology and Oncology, University Hospital Regensburg, Regensburg, Germany.
Ernst HollerDepartment of Hematology and Oncology, University Hospital Regensburg, Regensburg, Germany.
Andreas MackensenDepartment of Medicine 5, University Hospital Erlangen, University of Erlangen-Nuremberg, Erlangen, Germany.
Markus F NeurathDepartment of Medicine 1, University Hospital Erlangen, University of Erlangen-Nuremberg, Kussmaul Campus for Medical Research, Erlangen, Germany.
Kai HildnerDepartment of Medicine 1, University Hospital Erlangen, University of Erlangen-Nuremberg, Kussmaul Campus for Medical Research, Erlangen, Germany.
Friedrich-Alexander-Universität Erlangen-Nürnberg · DEUniversity Hospital Regensburg · DEGoethe University Frankfurt · DEChristian-Albrechts-Universität zu Kiel · DEHeidelberg University · DEUniversitätsklinikum Erlangen · DEUniversity of Würzburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute graft-versus-host disease (GVHD) represents a severe, T cell-driven inflammatory complication following allogeneic hematopoietic cell transplantation (allo-HCT). GVHD often affects the intestine and is associated with a poor prognosis. Although frequently detectable, proinflammatory mechanisms exerted by intestinal tissue-infiltrating Th cell subsets remain to be fully elucidated. Here, we show that the Th17-defining transcription factor basic leucine zipper transcription factor ATF-like (BATF) was strongly regulated across human and mouse intestinal GVHD tissues. Studies in complete MHC-mismatched and minor histocompatibility-mismatched (miHA-mismatched) GVHD models revealed that BATF-expressing T cells were functionally indispensable for intestinal GVHD manifestation. Mechanistically, BATF controlled the formation of colon-infiltrating, IL-7 receptor-positive (IL-7R+), granulocyte-macrophage colony-stimulating factor-positive (GM-CSF+), donor T effector memory (Tem) cells. This T cell subset was sufficient to promote intestinal GVHD, while its occurrence was largely dependent on T cell-intrinsic BATF expression, required IL-7-IL-7R interaction, and was enhanced by GM-CSF. Thus, this study identifies BATF-dependent pathogenic GM-CSF+ effector T cells as critical promoters of intestinal inflammation in GVHD and hence putatively provides mechanistic insight into inflammatory processes previously assumed to be selectively Th17 driven.

Indexed as

AnimalsBasic-Leucine Zipper Transcription FactorsBiopsyColonFemaleGraft vs Host DiseaseGranulocyte-Macrophage Colony-Stimulating FactorHematopoietic Stem Cell TransplantationHumansInflammationInterleukin-7 Receptor alpha SubunitIntestinesMajor Histocompatibility ComplexMiceMice, Inbred BALB CMice, Inbred C57BLBasic-Leucine Zipper Transcription FactorsBATF protein, humanBatf protein, mouseGranulocyte-Macrophage Colony-Stimulating FactorIL7R protein, humanInterleukin-7 Receptor alpha SubunitBone marrow transplantationCytokinesGastroenterologyImmunologyT cells

Identifiers

PMID29376889
PMCPMC5824870
OpenAlexW2786158906

What OpenQuestion holds

Textmetadata
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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.