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Related Experiment Video

Updated: May 5, 2026

Lymphocyte Isolation from Human Skin for Phenotypic Analysis and Ex Vivo Cell Culture
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Immunohistochemistry Revealed Distinct IL-36γ Localization Among Different Skin Diseases.

Megumi Kishimoto1, Miho Kimura-Sashikawa1, Mayumi Komine1

  • 1Department of Dermatology, Jichi Medical University, Tochigi, Japan.

The Journal of Dermatology
|May 4, 2026
PubMed
Summary

Interleukin-36 gamma (IL-36γ) is elevated in psoriatic skin, but its expression and nuclear localization vary across inflammatory skin diseases. This suggests distinct pathogenic roles and potential disease-specific patterns for IL-36γ.

Keywords:
Interleukin‐36generalized pustular psoriasisimmunohistochemistrypsoriasispyoderma gangrenosum

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Area of Science:

  • Immunodermatology
  • Molecular Dermatology
  • Inflammatory Skin Diseases

Background:

  • Interleukin-36 gamma (IL-36γ) is implicated in psoriasis pathogenesis, driving neutrophil recruitment.
  • The precise localization of IL-36γ within psoriatic epidermis and its differential expression in other inflammatory skin conditions are not fully understood.

Purpose of the Study:

  • To investigate and compare the epidermal localization and nuclear positivity of IL-36γ in various inflammatory skin diseases, including psoriasis vulgaris and generalized pustular psoriasis.
  • To determine if IL-36γ expression patterns can differentiate between psoriasis and other skin conditions.

Main Methods:

  • Immunohistochemistry was employed to analyze IL-36γ expression in skin biopsies from patients with psoriasis vulgaris, generalized pustular psoriasis, pyoderma gangrenosum, atopic dermatitis, and other inflammatory skin diseases.
  • Staining intensity, distribution, and nuclear positivity of IL-36γ were quantitatively assessed and compared across disease groups.

Main Results:

  • IL-36γ was strongly expressed in the upper epidermis of psoriasis vulgaris and generalized pustular psoriasis, with significantly higher scores than in atopic dermatitis and normal skin.
  • Expression levels in pyoderma gangrenosum, palmoplantar pustulosis, and drug-induced eruptions were comparable to psoriasis.
  • Nuclear IL-36γ staining was prevalent in psoriasis (92-100%) but absent in pyoderma gangrenosum, a statistically significant difference.

Conclusions:

  • IL-36γ is upregulated in various inflammatory skin diseases, not exclusively psoriasis.
  • The distinct pattern of nuclear IL-36γ localization in psoriasis compared to pyoderma gangrenosum suggests potential disease-specific roles.
  • Further research is needed to elucidate the biological significance and mechanisms underlying IL-36γ's nuclear localization and its implications in skin inflammation.