Evidence map›Paper›PMID 42258456›Full record

ArticlePloS one2026

Expression of melanoma differentiation-associated gene 5 in the epidermis and cutaneous deposition of complement C3 and immunoglobulins in patients with dermatomyositis.

Yoshiaki Zaizen, Takuma Koga, Masahiro Tsutsumi, Shinjiro Kaieda, Jun Akiba, Takekuni Nakama, Tomoaki Hoshino

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

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No citing paper in PubMed yet.

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

7 authors.

Yoshiaki ZaizenDivision of Respirology, Neurology and Rheumatology, Department of Medicine, Kurume University School of Medicine, Fukuoka, Japan.ORCID https://orcid.org/0000-0003-2274-4599
Takuma KogaDivision of Respirology, Neurology and Rheumatology, Department of Medicine, Kurume University School of Medicine, Fukuoka, Japan.
Masahiro TsutsumiDepartment of Dermatology, Kurume University School of Medicine, Fukuoka, Japan.
Shinjiro KaiedaDivision of Respirology, Neurology and Rheumatology, Department of Medicine, Kurume University School of Medicine, Fukuoka, Japan.
Jun AkibaDepartment of Pathology, Kurume University School of Medicine, Fukuoka, Japan.
Takekuni NakamaDepartment of Dermatology, Kurume University School of Medicine, Fukuoka, Japan.
Tomoaki HoshinoDivision of Respirology, Neurology and Rheumatology, Department of Medicine, Kurume University School of Medicine, Fukuoka, Japan.ORCID https://orcid.org/0000-0002-0459-4913

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesDermatomyositis (DM) is an autoimmune disease characterized by interface dermatitis, but the immunopathological features underlying cutaneous inflammation remain incompletely understood. The aim of this study was to characterize the cutaneous deposition of complement and immunoglobulins, as well as to clarify the localization of melanoma differentiation-associated gene 5 (MDA5) in DM skin.

methodsSkin biopsy specimens from 22 patients with DM and 13 control specimens obtained from cancer-free skin of patients with dermatofibrosarcoma protuberans were examined. Immunohistochemical staining for complement C3c, immunoglobulins (IgG, IgM, and IgA), and MDA5 was semi-quantitatively evaluated, focusing on the superficial dermis near the dermo-epidermal junction.

resultsSignificantly greater deposition of C3c, IgM, and IgA was exhibited by DM skin compared with control skin (all p ≤ 0.001), predominantly localised to the superficial dermis at sites of interface dermatitis. In contrast, IgG showed comparable deposition in both DM and control skin. MDA5 was strongly expressed in the stratum spinosum and basal layer of the epidermis in both DM and control skin. Enhanced MDA5 expression was notably observed in dermal inflammatory cells and capillaries in DM skin, but minimal expression was observed in the dermis of control skin.

conclusionsDM skin is characterized by the deposition of immunoglobulins and complement C3c at sites of interface dermatitis, findings that are consistent with immune complex-mediated injury. MDA5 is widely expressed in both DM and control skin epidermis and can be detected in the infiltrating inflammatory cells of DM.

Indexed as

Complement C3DermatomyositisEpidermisImmunoglobulinsInterferon-Induced Helicase, IFIH1AdultAgedFemaleHumansMaleMiddle AgedSkinComplement C3IFIH1 protein, humanImmunoglobulinsInterferon-Induced Helicase, IFIH1

Identifiers

PMID42258456
PMCPMC13245797

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