Allergology International (Jan 2013)

Role of Interleukin-33 in Innate-Type Immune Cells in Allergy

  • Susumu Nakae,
  • Hideaki Morita,
  • Tatsukuni Ohno,
  • Ken Arae,
  • Kenji Matsumoto,
  • Hirohisa Saito

DOI
https://doi.org/10.2332/allergolint.13-RAI-0538
Journal volume & issue
Vol. 62, no. 1
pp. 13 – 20

Abstract

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Interleukin-33 (IL-33), a member of the IL-1 cytokine family, is preferentially and constitutively expressed in epithelial cells, and it is especially localized in the cells' nucleus. The nuclear IL-33 is released by necrotic cells after tissue injury and/or trauma, and subsequently provokes local inflammation as an alarmin, like high-mobility group box protein-1 (HMGB-1) and IL-1α. IL-33 mainly activates Th2 cells and such innate-type immune cells as mast cells, basophils, eosinophils and natural helper cells that express IL-33R (a heterodimer of IL-1 receptor-like 1 [IL-1RL1; also called ST2, T1, Der4, fit-1] and IL-1 receptor accessory protein [IL-1RAcP]). That activation causes the cells to produce Th2 cytokines, which contribute to host defense against nematodes. On the other hand, excessive and/or inappropriate production of IL-33 is also considered to be involved in the development of such disorders as allergy. In this review, we summarize current knowledge regarding the pathogenic roles of IL-33 in the development of allergic inflammation by focusing on its effects on innate-type immune cells.

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