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Lupus ; 17(4): 289-94, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18413409

ABSTRACT

Previous reports have suggested that regulatory T cells (Treg) are abnormal in patients with systemic lupus erythematosus (SLE). In the present work, we quantified CD4+FOXP3+ Treg cells in patients with SLE and found no quantitative alterations. However, we found a clear defect in suppression assays. Surprisingly, SLE-derived Treg cells exhibited a normal phenotype and functional capacity. Conversely, SLE-derived CD4+CD25(-) effector T cells resisted suppression by autologous and allogeneic regulatory cells. Our findings strongly suggest that the defect in T-cell suppression observed in SLE is because of effector cell resistance and not because of an abnormal regulatory function.


Subject(s)
Immunity, Cellular , Lupus Erythematosus, Systemic/immunology , T-Lymphocytes, Regulatory/immunology , Adult , Cell Proliferation , Cells, Cultured , Female , Flow Cytometry , Forkhead Transcription Factors/biosynthesis , Forkhead Transcription Factors/genetics , Gene Expression , Humans , Interleukin-2 Receptor alpha Subunit/immunology , Lupus Erythematosus, Systemic/genetics , Lupus Erythematosus, Systemic/pathology , Male , Polymerase Chain Reaction , RNA/genetics , T-Lymphocytes, Regulatory/metabolism , T-Lymphocytes, Regulatory/pathology
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