Evidence map›Paper›PMID 29572462›Full record

ArticleScientific reports2018

Regulation of IL-22BP in psoriasis.

Stefanos Voglis, Sonja Moos, Luise Kloos, Florian Wanke, Morad Zayoud, Penelope Pelczar, Anastasios D Giannou, Silvia Pezer, Michael Albers, Felix Luessi and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

25 citing papers in PubMed, 36 citations in OpenAlex.

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  10. The role of IL-22 in cancer.Medical oncology (Northwood, London, England) · 2024
    Review
  11. The role of Interleukin-22 in severe acute pancreatitis.Molecular medicine (Cambridge, Mass.) · 2024
    Review
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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 4 institutions in 1 country.

Stefanos VoglisInstitute for Molecular Medicine, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.
Sonja MoosInstitute for Molecular Medicine, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.
Luise KloosInstitute for Molecular Medicine, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.
Florian WankeInstitute for Molecular Medicine, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.
Morad ZayoudInstitute for Molecular Medicine, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.
Penelope PelczarI. Medizinische Klinik und Poliklinik, Universitätsklinikum Hamburg-Eppendorf, 20246, Hamburg, Germany.
Anastasios D GiannouI. Medizinische Klinik und Poliklinik, Universitätsklinikum Hamburg-Eppendorf, 20246, Hamburg, Germany.
Silvia PezerDepartment of Dermatology, Heidelberg University Hospital, 69120, Heidelberg, Germany.
Michael AlbersDepartment of Research, Phenex Pharmaceuticals AG, Heidelberg, Germany.
Felix LuessiDepartment of Neurology, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Samuel HuberI. Medizinische Klinik und Poliklinik, Universitätsklinikum Hamburg-Eppendorf, 20246, Hamburg, Germany.
Knut SchäkelDepartment of Dermatology, Heidelberg University Hospital, 69120, Heidelberg, Germany.
Florian C KurschusInstitute for Molecular Medicine, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany. florian.kurschus@uni-heidelberg.de.ORCID 0000-0001-7550-0681
Johannes Gutenberg University Mainz · DEUniversität Hamburg · DEHeidelberg University · DEPhenex Pharmaceuticals (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IL-22 is a potent pro-inflammatory cytokine upregulated in psoriasis and in other inflammatory diseases. The function of IL-22 is regulated by the soluble scavenging receptor, IL-22 binding protein (IL-22BP or IL-22RA2). However, the role and regulation of IL-22BP itself in the pathogenesis of inflammatory disease remain unclear. We used the TLR7 agonist Imiquimod (IMQ) to induce a psoriasis-like skin disease in mice and found a strong downregulation of IL-22BP in the affected skin as well as in the lymph nodes of animals treated with IMQ. We also analysed psoriatic skin of patients and compared this to skin of healthy donors. Interestingly, IL-22BP expression was similarly downregulated in skin biopsies of psoriasis patients compared to the skin of healthy donors. Since IL-22BP is expressed foremost in dendritic cells, we characterized its expression in monocyte-derived dendritic cells (MoDC) during maturation. In this way, we found Prostaglandin E2 (PGE

Indexed as

AnimalsCells, CulturedDendritic CellsDinoprostoneDisease Models, AnimalFemaleHumansMiceMice, Inbred BALB CPsoriasisReceptors, InterleukinSkinDinoprostoneIL22RA2 protein, humaninterleukin-22 receptorReceptors, Interleukin

Identifiers

PMID29572462
PMCPMC5865214
OpenAlexW2794208442

What OpenQuestion holds

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Registered trials

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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.