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Experimental & Molecular Medicine ; : 187-194, 2010.
Artigo em Inglês | WPRIM | ID: wpr-203594

RESUMO

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.


Assuntos
Animais , Camundongos , Células Apresentadoras de Antígenos/efeitos dos fármacos , Artrite Experimental/imunologia , Galinhas , Colágeno Tipo II/imunologia , Tolerância Imunológica/efeitos dos fármacos , Camundongos Endogâmicos BALB C , Ovalbumina/imunologia , Células Th1/efeitos dos fármacos , Células Th2/efeitos dos fármacos , Fator de Crescimento Transformador beta2/farmacologia
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