Evidence map›Paper›PMID 35357743›Full record

ArticleEMBO reports2022

Helminthic dehydrogenase drives PGE

Ulrich Fabien Prodjinotho, Vitka Gres, Fiona Henkel, Matthew Lacorcia, Ramona Dandl, Martin Haslbeck, Veronika Schmidt, Andrea Sylvia Winkler, Chummy Sikasunge, Per-Johan Jakobsson and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

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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

13 authors at 8 institutions in 4 countries.

Ulrich Fabien ProdjinothoInstitute for Medical Microbiology, Immunology and Hygiene, TUM School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Vitka Gres *Institute for Immunodeficiency, Center for Chronic Immunodeficiency, Medical Center and Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Fiona Henkel *Center of Allergy and Environment (ZAUM), Technical University of Munich and Helmholtz Center Munich, Munich, Germany.ORCID 0000-0003-3198-2046
Matthew LacorciaInstitute for Medical Microbiology, Immunology and Hygiene, TUM School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Ramona DandlDepartment of Chemistry, Technical University Munich (TUM), Garching, Germany.ORCID 0000-0002-9290-4394
Martin HaslbeckDepartment of Chemistry, Technical University Munich (TUM), Garching, Germany.
Veronika SchmidtCenter for Global Health, TUM School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Andrea Sylvia WinklerCenter for Global Health, TUM School of Medicine, Technical University of Munich (TUM), Munich, Germany.ORCID 0000-0003-3131-6983
Chummy SikasungeDepartment of Paraclinicals, School of Veterinary Medicine, University of Zambia, Lusaka, Zambia.ORCID 0000-0002-5564-2655
Per-Johan JakobssonRheumatology Unit, Department of Medicine, Solna, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0001-7665-9715
Philipp HennekeInstitute for Immunodeficiency, Center for Chronic Immunodeficiency, Medical Center and Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0001-7314-7984
Julia Esser-von BierenCenter of Allergy and Environment (ZAUM), Technical University of Munich and Helmholtz Center Munich, Munich, Germany.ORCID 0000-0003-1898-9382
Clarissa Prazeres da CostaInstitute for Medical Microbiology, Immunology and Hygiene, TUM School of Medicine, Technical University of Munich (TUM), Munich, Germany.ORCID 0000-0001-7996-4838
Helmholtz Zentrum München · DEInstitute of Medical Microbiology and Hygiene · DETechnical University of Munich · DEUniversity of Freiburg · DEUniversity of Oslo · NOGerman Center for Infection Research · DEKarolinska University Hospital · SEUniversity of Zambia · ZM

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunoregulation of inflammatory, infection-triggered processes in the brain constitutes a central mechanism to control devastating disease manifestations such as epilepsy. Observational studies implicate the viability of Taenia solium cysts as key factor determining severity of neurocysticercosis (NCC), the most common cause of epilepsy, especially in children, in Sub-Saharan Africa. Viable, in contrast to decaying, cysts mostly remain clinically silent by yet unknown mechanisms, potentially involving Tregs in controlling inflammation. Here, we show that glutamate dehydrogenase from viable cysts instructs tolerogenic monocytes to release IL-10 and the lipid mediator PGE

Indexed as

CystsDinoprostoneChildHumansInterleukin-10MonocytesOxidoreductasesT-Lymphocytes, RegulatoryDinoprostoneInterleukin-10Oxidoreductasesglutamate dehydrogenaseimmune regulationProstaglandin E2Taenia solium cystTreg cells

Identifiers

PMID35357743
PMCPMC9066053
OpenAlexW4220887467

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.