Assessment of tissue FoxP3+, CD4+ and CD8+ T-cells in active and stable nonsegmental vitiligo

Int J Dermatol. 2014 Aug;53(8):940-6. doi: 10.1111/ijd.12160. Epub 2014 Feb 14.

Abstract

Background: The exact etiology of vitiligo remains obscure. Studies have indicated a role for cellular immunity in the pathogenesis of vitiligo. The aim of this study is to assess tissue FoxP3+ natural regulatory T-cells (Tregs), as well as CD4+ and CD8+ T-cells in active vs. stable nonsegmental vitiligo.

Materials and methods: Immunohistochemical double-staining for expression of CD4+ and CD8+ T-cells with immunostaining for expression of FoxP3 in lesional, marginal, and nonlesional skin of nonsegmental vitiligo was used to evaluate the abundance of Tregs among CD4+ and CD8+ T-cells in active and stable cases of vitiligo.

Results: A significant increase in the number of CD4+ and CD8+ T-cells and a highly significant reduction in the number of FoxP3-expressing Tregs were detected in marginal skin in both stable and active vitiligo cases. FoxP3+ cells were decreased in tissue of patients with vitiligo compared with healthy controls. The number of CD8+ T-cells was increased in the epidermis and dermoepidermal junction (DEJ) in comparison with the number of CD4+ T-cells. Tregs were mostly present at the DEJ.

Conclusion: The reduction in the number of FoxP3+ cells in the marginal skin suggests that this is the site where regulatory activity is needed to suppress the activity of helper and cytotoxic T-cells that are actively contributing to depigmentation.

MeSH terms

  • Adolescent
  • Adult
  • CD4 Lymphocyte Count
  • CD4-Positive T-Lymphocytes / cytology*
  • CD8-Positive T-Lymphocytes / chemistry
  • CD8-Positive T-Lymphocytes / cytology*
  • Case-Control Studies
  • Dermis / chemistry
  • Dermis / immunology*
  • Epidermis / chemistry
  • Epidermis / immunology*
  • Female
  • Forkhead Transcription Factors / analysis*
  • Humans
  • Immunity, Cellular
  • Immunohistochemistry
  • Male
  • Prospective Studies
  • T-Lymphocytes, Regulatory / chemistry
  • T-Lymphocytes, Regulatory / cytology*
  • Vitiligo / immunology*
  • Young Adult

Substances

  • FOXP3 protein, human
  • Forkhead Transcription Factors