| Literature DB >> 20164680 |
Sundo Jung1, Yoon-Kyung Park, Hyunji Lee, Jung Hoon Shin, Gap Ryol Lee, Se-Ho Park.
Abstract
Collagen-induced arthritis (CIA) is mediated by self-reactive CD4(+) T cells that produce inflammatory cytokines. TGF-beta(2)-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.Entities:
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Year: 2010 PMID: 20164680 PMCID: PMC2845003 DOI: 10.3858/emm.2010.42.3.019
Source DB: PubMed Journal: Exp Mol Med ISSN: 1226-3613 Impact factor: 8.718