2012/05/07 by Simona Ruggieri, Maria Antonia Frassanito, Rosanna Dammacco +1 · 1 citation
Medicine · #Ocular Diseases and Behçet’s Syndrome #IgG4-Related and Inflammatory Diseases #Vasculitis and related conditions #FOXP3 #Medicine #Uveitis #IL-2 receptor #Immunology #Regulatory T cell #Population #Peripheral blood mononuclear cell #T cell #Monoclonal antibody #Antibody #Immune system #Biology #In vitro
paper · doi:10.3109/09273948.2012.681830
openalex publication_date 2012/05/07 · openalex created_date 2016/06/24 · openalex updated_date 2026/07/29
PURPOSE: To evaluate circulating CD4(+)CD25(+) regulatory T-cell populations in patients with autoimmune uveitis and to assess whether T-regulatory cell populations correlate with clinical features. METHODS: Sixty-four patients with noninfectious uveitis were enrolled. Following isolation and purification of peripheral blood mononuclear cells, Tregs were analyzed by assessing FOXP3 expression on T cells with an APC anti-human FOXP3 staining kit. Samples were simultaneously stained with anti-CD25-PeCy7, anti-CD3-FITC, anti-CD4-PercP, and anti-CD152 (CTLA-4)-PE monoclonal antibodies. RESULTS: A decrease in CD4(+)CD25(+)FOXP3(+) T cells was detected in patients with active uveitis compared with healthy controls (p < .05). In patients achieving clinical remission, the percentage of CD4(+)CD25(+)FOXP3(+) T cells increased up to values comparable to those of healthy controls, in step with an increased expression of CTLA4. CONCLUSION: Therapy of autoimmune uveitis results in the increase of T-regulatory lymphocyte population and restoration of their functional state. These changes are likely to contribute to the patients' clinical improvement or disease regression.