Evidence map›Paper›PMID 35464417›Full record

ArticleFrontiers in immunology2022

The Mycotoxin Beauvericin Exhibits Immunostimulatory Effects on Dendritic Cells

Xiaoli Yang, Shafaqat Ali, Manman Zhao, Lisa Richter, Vanessa Schäfer, Julian Schliehe-Diecks, Marian Frank, Jing Qi, Pia-Katharina Larsen, Jennifer Skerra and 12 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. The mycotoxin Beauvericin is an uncompetitive inhibitor of Cathepsin B.Protein science : a publication of the Protein Society · 2025
    Article
  4. Review
  5. Evaluation of Beauvericin's activity and mode of action against all life stages ofFrontiers in cellular and infection microbiology · 2025
    Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. 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

22 authors at 7 institutions in 2 countries.

Xiaoli YangInstitute of Medical Microbiology and Hospital Hygiene, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Shafaqat AliInstitute of Medical Microbiology and Hospital Hygiene, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Manman ZhaoInstitutes of Brain Science, State Key Laboratory of Medical Neurobiology, Fudan University, Shanghai, China.
Lisa RichterInstitute of Medical Microbiology and Hospital Hygiene, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Vanessa SchäferInstitute of Medical Microbiology and Hospital Hygiene, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Julian Schliehe-DiecksDepartment of Pediatric Oncology, Hematology and Clinical Immunology, Medical Faculty, Heinrich-Heine University Düsseldorf, Düsseldorf, Germany.
Marian FrankInstitute of Pharmaceutical Biology and Biotechnology, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Jing QiInstitute for Transplantation Diagnostics and Cell Therapeutics, Medical Faculty, Heinrich-Heine University Düsseldorf, Düsseldorf, Germany.
Pia-Katharina LarsenInstitute for Experimental Infection Research, TWINCORE, Centre for Experimental and Clinical Infection Research, Helmholtz Centre for Infection Research and the Hannover Medical School, Hannover, Germany.
Jennifer SkerraInstitute for Experimental Infection Research, TWINCORE, Centre for Experimental and Clinical Infection Research, Helmholtz Centre for Infection Research and the Hannover Medical School, Hannover, Germany.
Heba IslamInstitute of Medical Microbiology, University Hospital of Essen, University of Duisburg-Essen, Essen, Germany.
Thorsten WachtmeisterBiological and Medical Research Center (BMFZ), Medical Faculty, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Christina AlterInstitute of Molecular Cardiology, Medical Faculty, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Anfei HuangInstitute for Systems Immunology, Julius-Maximilians-Universität of Würzburg (JMU), Würzburg, Germany.
Sanil BhatiaDepartment of Pediatric Oncology, Hematology and Clinical Immunology, Medical Faculty, Heinrich-Heine University Düsseldorf, Düsseldorf, Germany.
Karl KöhrerBiological and Medical Research Center (BMFZ), Medical Faculty, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Carsten KirschningInstitute of Medical Microbiology, University Hospital of Essen, University of Duisburg-Essen, Essen, Germany.
Heike WeighardtImmunology and Environment, Life & Medical Sciences (LIMES) Institute, University of Bonn, Bonn, Germany.
Ulrich KalinkeInstitute for Experimental Infection Research, TWINCORE, Centre for Experimental and Clinical Infection Research, Helmholtz Centre for Infection Research and the Hannover Medical School, Hannover, Germany.
Rainer KalscheuerInstitute of Pharmaceutical Biology and Biotechnology, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Markus UhrbergInstitute for Transplantation Diagnostics and Cell Therapeutics, Medical Faculty, Heinrich-Heine University Düsseldorf, Düsseldorf, Germany.
Stefanie ScheuInstitute of Medical Microbiology and Hospital Hygiene, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Heinrich Heine University Düsseldorf · DECenter for Experimental and Clinical Infection Research · DEUniversity of Duisburg-Essen · DEFudan University · CNHelmholtz Centre for Infection Research · DEUniversity of Bonn · DEUniversity of Würzburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Beauvericin (BEA), a mycotoxin of the enniatin family produced by various toxigenic fungi, has been attributed multiple biological activities such as anti-cancer, anti-inflammatory, and anti-microbial functions. However, effects of BEA on dendritic cells remain unknown so far. Here, we identified effects of BEA on murine granulocyte-macrophage colony-stimulating factor (GM-CSF)-cultured bone marrow derived dendritic cells (BMDCs) and the underlying molecular mechanisms. BEA potently activates BMDCs as signified by elevated IL-12 and CD86 expression. Multiplex immunoassays performed on myeloid differentiation primary response 88 (MyD88) and toll/interleukin-1 receptor (TIR) domain containing adaptor inducing interferon beta (TRIF) single or double deficient BMDCs indicate that BEA induces inflammatory cytokine and chemokine production in a MyD88/TRIF dependent manner. Furthermore, we found that BEA was not able to induce IL-12 or IFNβ production in Toll-like receptor 4 (

Indexed as

MycotoxinsToll-Like Receptor 4Adaptor Proteins, Vesicular TransportAnimalsCytokinesDendritic CellsDepsipeptidesHEK293 CellsHumansInterleukin-12MiceMyeloid Differentiation Factor 88Signal TransductionAdaptor Proteins, Vesicular TransportbeauvericinCytokinesDepsipeptidesInterleukin-12MycotoxinsMyeloid Differentiation Factor 88TLR4 protein, humanTlr4 protein, mouseToll-Like Receptor 4activatebeauvericindendritic cellsImmunostimulatory activitiesTLR4 (Toll-like receptor 4)

Identifiers

PMID35464417
PMCPMC9024221
OpenAlexW4225514402

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.