Interleukin 21 prevents antigen-induced IgE production by inhibiting germ line C transcription of IL-4–stimulated B cells

نویسندگان

  • Akira Suto
  • Hiroshi Nakajima
  • Koichi Hirose
  • Kotaro Suzuki
  • Shin-ichiro Kagami
  • Yohei Seto
  • Aihiro Hoshimoto
  • Yasushi Saito
  • Donald C. Foster
  • Itsuo Iwamoto
چکیده

Interleukin 21 (IL-21) has recently been identified as a multifunctional cytokine that induces the proliferation of T cells and B cells and differentiation of natural killer cells. To determine whether IL-21 regulates IL-4–mediated immune responses, we examined the effect of IL-21 on antigen-specific IgE production in mice. We also examined the effect of IL-21 on IL-4–induced IgE production from B cells and antigen-induced T-helper 2 (Th2) cell differentiation. The in vivo injection of IL-21 prevented antigen-specific IgE but not IgG2a production on immunization. IL-21 did not affect Th2 cell differentiation or IL-4 production from CD4 T cells but directly inhibited IL-4–induced IgE production from B cells at single-cell levels. Moreover, IL-21 inhibited IL-4– induced germ line C transcription in B cells without the inhibition of signal transducer and activator of transcription 6 (Stat6) activation. Taken together, these results indicate that IL-21 down-regulates IgE production from IL-4–stimulated B cells through the inhibition of germ line C transcription and thus suggest that IL-21 may be useful for the treatment of IgE-dependent allergic diseases. (Blood. 2002;100:4565-4573)

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تاریخ انتشار 2002