Characterization of the inflammatory infiltrate and cytokine expression in the skin of horses with recurrent urticaria

Vet Dermatol. 2012 Dec;23(6):503-e99. doi: 10.1111/j.1365-3164.2012.01117.x.

Abstract

Background: Recurrent urticaria (RU) is a common skin disease of horses, but little is known about its pathogenesis.

Hypothesis/objective: The aim of this study was to characterize the inflammatory cell infiltrate and cytokine expression pattern in the skin of horses with RU.

Animals: Biopsies of lesional and nonlesional skin of horses with RU (n = 8) and of skin from healthy control horses (n = 8) were evaluated.

Methods: The inflammatory cell infiltrate was analysed by routine histology. Immunohistochemistry was used to identify T cells (CD3), B ells (CD79), macrophages (MAC387) and mast cells (tryptase). Expression of T-helper 2 cytokines (interleukins IL-4, IL-5 and IL-13), a T-helper 1 cytokine (interferon-γ), IL-4 receptor α and thymic stromal lymphopoietin was assessed by quantitative RT-PCR. Results - In subepidermal lesional skin of RU-affected horses, increased numbers of eosinophils (P ≤ 0.01), CD79-positive (P ≤ 0.01), MAC387-positive (P ≤ 0.01) and tryptase-positive cells (P ≤ 0.05) were found compared with healthy horses. Subepidermal lesional skin of RU-affected horses contained more eosinophils (P ≤ 0.05) and tryptase-positive cells (P ≤ 0.05) compared with nonlesional skin. There was no significant difference in infiltrating cells between nonlesional skin and skin of healthy horses. Expression of IL-4 (P ≤ 0.01), IL-13 (P ≤ 0.05), thymic stromal lymphopoietin (P ≤ 0.05) and IL-4 receptor α (P ≤ 0.05) was increased in lesional skin of RU-affected horses compared with control horses. Expression of IL-4 was higher (P ≤ 0.05) in lesional compared with nonlesional RU skin.

Conclusions and clinical importance: Analysis of cytokine expression and inflammatory infiltrate suggests that T-helper 2 cytokines, eosinophils, mast cells and presumptive macrophages play a role in the pathogenesis of equine RU.

MeSH terms

  • Animals
  • Case-Control Studies
  • Cytokines / genetics
  • Cytokines / metabolism*
  • Gene Expression Regulation / immunology
  • Horse Diseases / metabolism*
  • Horse Diseases / pathology
  • Horses
  • Inflammation
  • Skin / cytology*
  • Skin / metabolism*
  • Transcriptome
  • Urticaria / metabolism
  • Urticaria / pathology
  • Urticaria / veterinary*

Substances

  • Cytokines