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Experimental & Molecular Medicine ; : 187-194, 2010.
Article in English | WPRIM | ID: wpr-203594

ABSTRACT

Collagen-induced arthritis (CIA) is mediated by self-reactive CD4+ T cells that produce inflammatory cytokines. TGF-beta2-treated tolerogenic antigen-presenting cells (Tol-APCs) are known to induce tolerance in various autoimmune diseases. In this study, we investigated whether collagen-specific Tol-APCs could induce suppression of CIA. We observed that Tol-APCs could suppress the development and severity of CIA and delay the onset of CIA. Treatment of Tol-APCs reduced the number of IFN-gamma- and IL-17-producing CD4+ T cells and increased IL-4- and IL-5-producing CD4+ T cells upon collagen antigen stimulation in vitro. The suppression of CIA conferred by Tol-APCs correlated with their ability to selectively induce IL-10 production. We also observed that treatment of Tol-APCs inhibited not only cellular immune responses but also humoral immune responses in the process of CIA. Our results suggest that in vitro-generated Tol-APCs have potential therapeutic value for the treatment of rheumatoid arthritis as well as other autoimmune diseases.


Subject(s)
Animals , Mice , Antigen-Presenting Cells/drug effects , Arthritis, Experimental/immunology , Chickens , Collagen Type II/immunology , Immune Tolerance/drug effects , Mice, Inbred BALB C , Ovalbumin/immunology , Th1 Cells/drug effects , Th2 Cells/drug effects , Transforming Growth Factor beta2/pharmacology
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