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

disease memory disease recurrence inflammation polymorphic light eruption resident memory T cell (TrM) sun allergy

Journal

Frontiers in medicine
ISSN: 2296-858X
Titre abrégé: Front Med (Lausanne)
Pays: Switzerland
ID NLM: 101648047

Informations de publication

Date de publication:
2022
Historique:
received: 30 03 2022
accepted: 16 05 2022
entrez: 27 6 2022
pubmed: 28 6 2022
medline: 28 6 2022
Statut: epublish

Résumé

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

Identifiants

pubmed: 35755042
doi: 10.3389/fmed.2022.908047
pmc: PMC9226321
doi:

Types de publication

Journal Article

Langues

eng

Pagination

908047

Informations de copyright

Copyright © 2022 Patra, Strobl, Atzmüller, Reininger, Kleissl, Gruber-Wackernagel, Nicolas, Stary, Vocanson and Wolf.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

VijayKumar Patra (V)

Centre 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.
Research Unit for Photodermatology, Medical University of Graz, Graz, Austria.

Johanna Strobl (J)

Department of Dermatology, Medical University of Vienna, Vienna, Austria.

Denise Atzmüller (D)

Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.

Bärbel Reininger (B)

Department of Dermatology, Medical University of Vienna, Vienna, Austria.

Lisa Kleissl (L)

Department of Dermatology, Medical University of Vienna, Vienna, Austria.
Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.

Alexandra Gruber-Wackernagel (A)

Research Unit for Photodermatology, Medical University of Graz, Graz, Austria.

Jean-Francois Nicolas (JF)

Allergy and Clinical Immunology Department, Lyon Sud University Hospital, Pierre-Bénite, France.

Georg Stary (G)

Department of Dermatology, Medical University of Vienna, Vienna, Austria.
Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.
CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.

Marc Vocanson (M)

Centre 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 Wolf (P)

Research Unit for Photodermatology, Medical University of Graz, Graz, Austria.

Classifications MeSH