TNF-alpha is crucial for the development of autoimmune arthritis in IL-1 receptor antagonist-deficient mice.

نویسندگان

  • Reiko Horai
  • Akiko Nakajima
  • Katsuyoshi Habiro
  • Motoko Kotani
  • Susumu Nakae
  • Taizo Matsuki
  • Aya Nambu
  • Shinobu Saijo
  • Hayato Kotaki
  • Katsuko Sudo
  • Akihiko Okahara
  • Hidetoshi Tanioka
  • Toshimi Ikuse
  • Naoto Ishii
  • Pamela L Schwartzberg
  • Ryo Abe
  • Yoichiro Iwakura
چکیده

IL-1 receptor antagonist-deficient (IL-1Ra(-/-)) mice spontaneously develop autoimmune arthritis. We demonstrate here that T cells are required for the induction of arthritis; T cell-deficient IL-1Ra(-/-) mice did not develop arthritis, and transfer of IL-1Ra(-/-) T cells induced arthritis in nu/nu mice. Development of arthritis was also markedly suppressed by TNF-alpha deficiency. We found that TNF-alpha induced OX40 expression on T cells and blocking the interaction between either CD40 and its ligand or OX40 and its ligand suppressed development of arthritis. These findings suggest that IL-1 receptor antagonist deficiency in T cells disrupts homeostasis of the immune system and that TNF-alpha plays an important role in activating T cells through induction of OX40.

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عنوان ژورنال:
  • The Journal of clinical investigation

دوره 114 11  شماره 

صفحات  -

تاریخ انتشار 2004