Evidence map›Paper›PMID 35755042›Full record

ArticleFrontiers in medicine2022

Accumulation of Cytotoxic Skin Resident Memory T Cells and Increased Expression of IL-15 in Lesional Skin of Polymorphic Light Eruption.

VijayKumar Patra, Johanna Strobl, Denise Atzmüller, Bärbel Reininger, Lisa Kleissl, Alexandra Gruber-Wackernagel, Jean-Francois Nicolas, Georg Stary, Marc Vocanson, Peter Wolf

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

5 citing papers in PubMed, 17 citations in OpenAlex.

  1. 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

10 authors at 5 institutions in 2 countries.

VijayKumar PatraCentre International de Recherche en Infectiologie, Institut National de la Santé et de la Recherche Médicale, U1111, Université Claude Bernard Lyon 1, Centre National de la Recherche Scientifique, UMR 5308, Ecole Normale Supérieure de Lyon, Université de Lyon, Lyon, France.
Johanna StroblDepartment of Dermatology, Medical University of Vienna, Vienna, Austria.
Denise AtzmüllerLudwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.
Bärbel ReiningerDepartment of Dermatology, Medical University of Vienna, Vienna, Austria.
Lisa KleisslDepartment of Dermatology, Medical University of Vienna, Vienna, Austria.
Alexandra Gruber-WackernagelResearch Unit for Photodermatology, Medical University of Graz, Graz, Austria.
Jean-Francois NicolasAllergy and Clinical Immunology Department, Lyon Sud University Hospital, Pierre-Bénite, France.
Georg StaryDepartment of Dermatology, Medical University of Vienna, Vienna, Austria.
Marc VocansonCentre International de Recherche en Infectiologie, Institut National de la Santé et de la Recherche Médicale, U1111, Université Claude Bernard Lyon 1, Centre National de la Recherche Scientifique, UMR 5308, Ecole Normale Supérieure de Lyon, Université de Lyon, Lyon, France.
Peter WolfResearch Unit for Photodermatology, Medical University of Graz, Graz, Austria.
Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases · ATMedical University of Graz · ATMedical University of Vienna · ATÉcole Normale Supérieure de Lyon · FRHospices Civils de Lyon · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with polymorphic light eruption (PLE) develop lesions upon the first exposure to sun in spring/summer, but lesions usually subside during season due to the natural (or medical) photohardening. However, these lesions tend to reappear the following year and continue to do so in most patients, suggesting the presence of a disease memory. To study the potential role of skin resident memory T cells (Trm), we investigated the functional phenotype of Trm and the expression of IL-15 in PLE. IL-15 is known to drive Trm proliferation and survival. Multiplex immunofluorescence was used to quantify the expression of CD3, CD4, CD8, CD69, CD103, CD49a, CD11b, CD11c, CD68, granzyme B (GzmB), interferon-gamma (IFN-γ), and IL-15 in formalin-fixed, paraffin-embedded lesional skin samples from PLE patients and healthy skin from control subjects. Unlike the constitutive T cell population in healthy skin, a massive infiltration of T cells in the dermis and epidermis was observed in PLE, and the majority of these belonged to CD8

Indexed as

disease memorydisease recurrenceinflammationpolymorphic light eruptionresident memory T cell (TrM)sun allergy

Identifiers

PMID35755042
PMCPMC9226321
OpenAlexW4281625437

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.