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Regulatory T cells in the skin lesions and blood of patients with systemic sclerosis and morphoea
Author(s) -
Antiga E.,
Quaglino P.,
Bellandi S.,
Volpi W.,
Del Bianco E.,
Comessatti A.,
OsellaAbate S.,
De Simone C.,
Marzano A.,
Bernengo M.G.,
Fabbri P.,
Caproni M.
Publication year - 2010
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/j.1365-2133.2010.09633.x
Subject(s) - foxp3 , scleroderma (fungus) , medicine , fibrosis , immunology , connective tissue disease , immune system , transforming growth factor , pathogenesis , autoimmunity , connective tissue , il 2 receptor , autoimmune disease , cytokine , pathology , antibody , t cell , inoculation
Summary Background Systemic sclerosis (SSc) and morphoea are connective tissue diseases characterized by fibrosis of the skin. Although to date their pathogenesis has not been clearly defined, it is thought that autoimmunity may play a role in the development of the skin lesions observed in both these diseases. As regulatory T cells (Tregs) play a key role in the modulation of immune responses, it has recently been suggested that Treg impairment may lead to the development of autoimmune diseases. Objectives To investigate the presence of Tregs and their immunomodulatory cytokines, transforming growth factor (TGF)‐β and interleukin (IL)‐10, in patients with SSc and morphoea. Patients/methods Fifteen patients with SSc and 15 with morphoea were enrolled. Immunohistochemistry was applied to identify FoxP3+ (forkhead/winged helix transcription factor) Tregs, TGF‐β+ cells and IL‐10+ cells in the skin, cytofluorometry to detect CD4+CD25+FoxP3+ Tregs in the blood, and enzyme‐linked immunosorbent assays to analyse TGF‐β and IL‐10 serum levels. Results Fewer FoxP3+ Tregs and TGF‐β + and IL‐10+ cells were found in the skin of patients with scleroderma than in controls. Similarly, there were reduced TGF‐β and IL‐10 serum levels and fewer circulating CD4+CD25brightFoxP3+ cells in patients with SSc or morphoea, than in controls. Conclusions The quantitative reduction of Tregs, together with that of TGF‐β and IL‐10 serum levels, may be responsible for the loss of tolerance observed in both SSc and morphoea.