IL-12p40 Homodimer Ameliorates Experimental Autoimmune Arthritis.

نویسندگان

  • Seon-Yeong Lee
  • Young Ok Jung
  • Doo-Jin Kim
  • Chang-Min Kang
  • Young-Mee Moon
  • Yu-Jung Heo
  • Hye-Jwa Oh
  • Seong-Jeong Park
  • Se-Hwan Yang
  • Seung Ki Kwok
  • Ji-Hyeon Ju
  • Sung-Hwan Park
  • Young Chul Sung
  • Ho-Youn Kim
  • Mi-La Cho
چکیده

IL-23 is the key cytokine that induces the expansion of Th17 cells. It is composed of p19 and p40 subunits of IL-12. The p40 subunit binds competitively to the receptor of IL-23 and blocks its activity. Our aim was to assess the preventive and therapeutic effect of the IL-12p40 homodimer (p40)2 subunit in autoimmune arthritis animal models. In the current study, using IL-1R antagonist-knockout mice and a collagen-induced arthritis model, we investigated the suppressive effect of (p40)2 on inflammatory arthritis. We demonstrated that the recombinant adenovirus-expressing mouse (p40)2 model prevented the development of arthritis when given before the onset of arthritis. It also decreased the arthritis index and joint erosions in the mouse model if transferred after arthritis was established. (p40)2 inhibited the production of inflammatory cytokines and Ag-specific T cell proliferation. It also induced CD4(+)CD25(+)Foxp3 regulatory T (Treg) cells in vitro and in vivo, whereas the generation of retinoic acid receptor-related organ receptor γt and Th17 cells was suppressed. The induction of Treg cells and the suppression of Th17 cells were mediated via activated STAT5 and suppressed STAT3. Our data suggest that (p40)2 suppressed inflammatory arthritis successfully. This could be a useful therapeutic approach in autoimmune arthritis to regulate the Th17/Treg balance and IL-23 signaling.

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عنوان ژورنال:
  • Journal of immunology

دوره 195 7  شماره 

صفحات  -

تاریخ انتشار 2015