Evidence map›Paper›PMID 37533580›Full record

ArticleJID innovations : skin science from molecules to population health2023

Inflammatory Cues Direct Skin-Resident Type 1 Innate Lymphoid Cells to Adopt a Psoriasis-Promoting Identity.

Beatrix D G Evers, Miriam Hils, Christoph Heuser, Inga M Hölge, Désirée Argiriu, Yuliya Skabytska, Susanne Kaesler, Christian Posch, Percy A Knolle, Tilo Biedermann

Open access · goldAbstract read
In one paragraph

Article in JID innovations : skin science from molecules to population health, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Psoriasis Area and Severity Index (PASI) Objectivisation by Flow Cytometry Analysis of Major Lymphocytes Subsets.Acta informatica medica : AIM : journal of the Society for Medical Informatics of Bosnia & Herzegovina : casopis Drustva za medicinsku informatiku BiH · 2023
    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

10 authors at 3 institutions in 2 countries.

Beatrix D G EversDepartment of Dermatology and Allergology, TUM School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Miriam HilsDepartment of Dermatology and Allergology, TUM School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Christoph HeuserLeibniz Institute for Immunotherapy, Department of Functional Immune Cell Modulation, Regensburg, Germany.
Inga M HölgeDepartment of Dermatology and Allergology, TUM School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Désirée ArgiriuDepartment of Dermatology and Allergology, TUM School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Yuliya SkabytskaDepartment of Dermatology and Allergology, TUM School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Susanne KaeslerDepartment of Dermatology and Allergology, TUM School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Christian PoschDepartment of Dermatology and Allergology, TUM School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Percy A KnolleInstitute of Molecular Immunology and Experimental Oncology, Technical University of Munich (TUM), Munich, Germany.
Tilo BiedermannDepartment of Dermatology and Allergology, TUM School of Medicine, Technical University of Munich (TUM), Munich, Germany.
Technical University of Munich · DELeibniz Association · DESigmund Freud Privatuniversität Wien · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Innate lymphoid cells (ILCs) are gatekeepers in barrier organs, where they maintain tissue integrity and contribute to host defense as well as tissue repair. Inappropriate activation of ILCs, however, can lead to immunopathology with detrimental results. In this study, we focused on type 1 ILCs (ILC1s), which under inflammatory conditions constitute a poorly defined population with ambiguous functions. To delineate the properties of ILC1s in skin pathology, we used the well-established mouse model of imiquimod-induced psoriasis. Although ILC1s represented a minority among cutaneous lymphocytes in vehicle-treated controls, they rapidly expanded during early psoriasis and ultimately increased by >20-fold. This rapid increase was verified using two additional psoriasis models. Inflammatory ILC1s from imiquimod-treated skin were defined as CD44

Identifiers

PMID37533580
PMCPMC10392090
OpenAlexW4366813782

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.