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Circulating CD4+ CD25brightFOXP3+ regulatory T-cells are significantly reduced in bullous pemphigoid patients.

Abstract
Bullous pemphigoid (BP) is the most frequent autoimmune bullous skin disease, characterised by auto-antibodies against the hemidesmosome complex. Recently, regulatory T cells (Tregs) have been implicated in the development of several autoimmune diseases; few data are available in BP, failing to demonstrate a role of this subset in disease pathogenesis. The aim of this study was to investigate the expression and phenotypes of different Tregs (CD4+ CD25brightFOXP3+ and CD8+ CD28- cells) in BP to clarify whether the depletion of this subset constitutes one mechanism of tolerance loss. The CD4+ CD25brightFOXP3 and CD8+ CD28- circulating subsets were determined by flow-cytometry in 26 untreated BP patients and compared with a group of age- and sex-matched healthy controls (HC, n = 30). Absolute and percentage values of the CD4+ CD25brightFOXP3+ cells were significantly reduced in BP compared with HC (median CD25brightFOXP3+ expression within CD4+ cells: 1.8 vs. 3.5%, p = 0.002); conversely, BP patients were characterised by a significant expansion of the CD25brightFOXP3- "activated" T-cell subset. CCR4 and CD62L were expressed on the majority of CD4+ CD25brightFOXP3+ cells (75.2 and 82.3%, respectively). No differences in the CD8+ CD28- subset were found between BP and HC. This is the first report showing a significant reduction of circulating CD4+ CD25brightFOXP3+ Treg frequency in BP patients.
AuthorsP Quaglino, E Antiga, A Comessatti, M Caproni, T Nardò, R Ponti, M Novelli, S Osella-Abate, P Fabbri, M G Bernengo
JournalArchives of dermatological research (Arch Dermatol Res) Vol. 304 Issue 8 Pg. 639-45 (Oct 2012) ISSN: 1432-069X [Electronic] Germany
PMID22310732 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • CD4 Antigens
  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • Interleukin-2 Receptor alpha Subunit
Topics
  • Aged
  • Aged, 80 and over
  • Blood Circulation (immunology)
  • CD4 Antigens (metabolism)
  • Cell Separation
  • Female
  • Flow Cytometry
  • Forkhead Transcription Factors (metabolism)
  • Humans
  • Interleukin-2 Receptor alpha Subunit (metabolism)
  • Male
  • Middle Aged
  • Pemphigoid, Bullous (immunology)
  • T-Lymphocyte Subsets (immunology)
  • T-Lymphocytes, Regulatory (immunology)

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