Evidence map›Paper›PMID 23980097›Full record

ArticleThe Journal of experimental medicine2013

The Nlrp3 inflammasome regulates acute graft-versus-host disease.

Dragana Jankovic, Jayanthi Ganesan, Michael Bscheider, Natalie Stickel, Felix C Weber, Greta Guarda, Marie Follo, Dietmar Pfeifer, Aubry Tardivel, Kristina Ludigs and 19 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 142 papers.

0numbers the graph read from it
0cells of the map it votes in
142citing papers in PubMed
9.5field-weighted citation impact, top 1% 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

142 citing papers in PubMed, 233 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Hyperacute Graft-Versus-Host Disease.Bone marrow transplantation · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Graft-Versus-Host Disease Mouse Models: A Clinical-Translational Perspective.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  18. Article
  19. Article
  20. Review

82 more citing papers are in PubMed but not listed here.

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

29 authors at 8 institutions in 3 countries.

Dragana JankovicDepartment of Dermatology, University Hospital, CH-8091 Zürich, Switzerland.
Jayanthi Ganesan
Michael Bscheider
Natalie Stickel
Felix C Weber
Greta Guarda
Marie Follo
Dietmar Pfeifer
Aubry Tardivel
Kristina Ludigs
Abdellatif Bouazzaoui
Katrin Kerl
Julius C Fischer
Tobias Haas
Annette Schmitt-Gräff
Anand Manoharan
Leonard Müller
Jürgen Finke
Stefan F Martin
Oliver Gorka
Christian Peschel
Jürgen Ruland
Marco Idzko
Justus Duyster
Ernst Holler
Lars E French
Hendrik Poeck
Emmanuel Contassot
Robert Zeiser
University Medical Center Freiburg · DEENT and Allergy · USTechnical University of Munich · DEUniversity Hospital of Zurich · CHUniversity of Lausanne · CHKlinikum rechts der Isar · DEUniversity of Freiburg · DEUniversity Hospital Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The success of allogeneic hematopoietic cell transplantation is limited by acute graft-versus-host disease (GvHD), a severe complication accompanied by high mortality rates. Yet, the molecular mechanisms initiating this disease remain poorly defined. In this study, we show that, after conditioning therapy, intestinal commensal bacteria and the damage-associated molecular pattern uric acid contribute to Nlrp3 inflammasome-mediated IL-1β production and that gastrointestinal decontamination and uric acid depletion reduced GvHD severity. Early blockade of IL-1β or genetic deficiency of the IL-1 receptor in dendritic cells (DCs) and T cells improved survival. The Nlrp3 inflammasome components Nlrp3 and Asc, which are required for pro-IL-1β cleavage, were critical for the full manifestation of GvHD. In transplanted mice, IL-1β originated from multiple intestinal cell compartments and exerted its effects on DCs and T cells, the latter being preferentially skewed toward Th17. Compatible with these mouse data, increased levels of active caspase-1 and IL-1β were found in circulating leukocytes and intestinal GvHD lesions of patients. Thus, the identification of a crucial role for the Nlrp3 inflammasome sheds new light on the pathogenesis of GvHD and opens a potential new avenue for the targeted therapy of this severe complication.

Indexed as

Acute DiseaseAnimalsApoptosis Regulatory ProteinsCARD Signaling Adaptor ProteinsCarrier ProteinsCaspase 1Cytoskeletal ProteinsDendritic CellsGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansInflammasomesInterleukin-17Interleukin-1betaIntestinal MucosaIntestinesApoptosis Regulatory ProteinsCARD Signaling Adaptor ProteinsCarrier ProteinsCaspase 1Cytoskeletal ProteinsInflammasomesInterleukin-17Interleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanNlrp3 protein, mousePycard protein, mouseTumor Necrosis Factors

Identifiers

PMID23980097
PMCPMC3782050
OpenAlexW2146496194

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.