IL-31 expression by inflammatory cells is preferentially elevated in atopic dermatitis

Acta Derm Venereol. 2012 Jan;92(1):24-8. doi: 10.2340/00015555-1191.

Abstract

Interleukin-31 (IL-31) is a recently discovered cytokine expressed in many human tissues, and predominantly by activated CD4(+) T cells. IL-31 signals through a heterodimeric receptor consisting of IL-31 receptor alpha (IL-31RA) and oncostatin M receptor beta (OSMR). Earlier studies have shown involvement of IL-31 and its receptor components IL-31RA and OSMR in atopic dermatitis, pruritus and Th2-weighted inflammation at the mRNA level. The aim of this study was to investigate IL-31 protein expression in skin of such conditions. Immunohistochemical staining for IL-31, IL-31RA and OSMR was performed in formalin-fixed paraffin-embedded biopsy specimens. IL-31 expression was increased in the inflammatory infiltrates from skin biopsies taken from subjects with atopic dermatitis, compared with controls (p ≤ 0.05). IL-31, IL-31RA and OSMR protein immunoreactivity was not increased in biopsies from subjects with other Th2-weighted and pruritic skin diseases. Our results confirm, at the protein level, the relationship between IL-31 expression and atopic dermatitis. Our results do not support a general relationship between expression of IL-31/IL-31R and pruritic or Th2-mediated diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alopecia Areata / metabolism
  • Analysis of Variance
  • Antigens, CD / metabolism
  • Antigens, Differentiation, Myelomonocytic / metabolism
  • Dermatitis, Atopic / immunology
  • Dermatitis, Atopic / metabolism*
  • Humans
  • Immunohistochemistry
  • Interleukins / immunology
  • Interleukins / metabolism*
  • Leukocyte Common Antigens / metabolism
  • Mycosis Fungoides / metabolism
  • Oncostatin M Receptor beta Subunit / metabolism
  • Prurigo / metabolism
  • Pruritus / immunology
  • Pruritus / metabolism*
  • Psoriasis / metabolism
  • Receptors, Interleukin / metabolism
  • Sezary Syndrome / metabolism
  • Th2 Cells / immunology
  • Th2 Cells / metabolism*

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • CD68 antigen, human
  • IL31 protein, human
  • IL31RA protein, human
  • Interleukins
  • Oncostatin M Receptor beta Subunit
  • Receptors, Interleukin
  • Leukocyte Common Antigens