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Characterization of CD3+CD4-CD8- (double negative) T cells in patients with systemic lupus erythematosus: activation markersDepartment of Immunology and Molecular Pathology, Royal Free and University College School of Medicine, London, UK
Department of Immunology and Molecular Pathology, Royal Free and University College School of Medicine, London, UK; Centre for Rheumatology, Department of Medicine, Royal Free and University College School of Medicine, London, UK
Department of Immunology and Molecular Pathology, Royal Free and University College School of Medicine, London, UK
Centre for Rheumatology, Department of Medicine, Royal Free and University College School of Medicine, London, UK
Department of Immunology and Molecular Pathology, Royal Free and University College School of Medicine, London, UK; Department of Immunology and Molecular Pathology, Royal Free and University College School of Medicine, Windeyer Research Institute, 46 Cleveland St, London W1T 4JF, UKp.lydyard{at}ucl.ac.uk Systemic lupus erythematosus (SLE) is characterized by B cell hyperactivity and the production of autoantibodies, some of which (antibodies to dsDNA) are thought to be pathogenic. T helper cells drive the production of autoantibodies and the aim of this study is to characterize phenotypically a subpopulation of T cells (the CD3+CD4-CD8-, double negative (DN) T cells) previously identified as helping to enhance anti-DNA antibodies in patients with SLE. Data were obtained using FACS staining of DN T cells that had been purified from PBMCs by magnetic bead separation.
The percentage of TCR ab
Key Words: activation markers double negative SLE T cells
Lupus, Vol. 11, No. 8,
493-500 (2002) This article has been cited by other articles:
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DN T cells was found to be significantly higher in patients with SLE as compared with controls (P ^ 0.02), although there was no significant increase in total percentage of DN T cells, which includes TCR gd 
