Analysis of the Expression and Function of Immunoglobulin-Like Transcript 4 (ILT4, LILRB2) in Dendritic Cells from Patients with Systemic Lupus Erythematosus
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Dendritic cells (DC) play an important role in the development and maintenance of immune tolerance. Although the inhibitory receptor ILT4/LILRB2 has been related with the tolerogenic phenotype of DC, the possible role of this receptor in the breakdown of DC tolerogenic function in systemic lupus erythematosus (SLE) has not been elucidated. In this study, we analyzed the expression and function of the inhibitory receptor ILT4 in DC from SLE patients. We found that the percentage of ILT4 positive plasmacytoid DC and myeloid DC is significantly diminished in SLE patients. Interestingly, ligation of ILT4 did not affect the maturation or immunogenic capability of DC in healthy controls. In contrast, in SLE patients we observed an inhibitory effect of ILT4 on the immunogenic capability of DC. ILT4 was shown not to have a crucial role in regulating the maturation and function of DC from healthy controls but is partially involved in the maturation process and immunogenic capability of DC from SLE patients, suggesting that other inhibitory receptors, involved in the regulation of DC tolerogenic function, may be impaired in this autoimmune disease. © 2016 Paola del Carmen Guerra-de Blas et al.
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azathioprine; chloroquine; cyclosporin; immunoglobulin like transcript 4 protein; methotrexate; mycophenolate mofetil; prednisone; protein; unclassified drug; cytokine; immunoglobulin receptor; leukocyte antigen; LILRB1 protein, human; LILRB2 protein, human; lipopolysaccharide; membrane protein; adult; Article; cell maturation; clinical article; controlled study; dendritic cell; female; human; human cell; immunogenicity; male; myeloid dendritic cell; plasmacytoid dendritic cell; protein expression; protein function; systemic lupus erythematosus; dendritic cell; drug effects; genetics; immunological tolerance; immunology; metabolism; phenotype; secretion (process); systemic lupus erythematosus; Adult; Antigens, CD; Cytokines; Dendritic Cells; Female; Humans; Immune Tolerance; Lipopolysaccharides; Lupus Erythematosus, Systemic; Male; Membrane Glycoproteins; Phenotype; Receptors, Immunologic
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