The role of IL-33/ST2L signals in the immune cells

Immunol Lett. 2015 Mar;164(1):11-7. doi: 10.1016/j.imlet.2015.01.008. Epub 2015 Feb 4.

Abstract

Interleukin (IL)-33 signals influence various immune cells during differentiation, immune responses and homeostasis. As discussed in this Review, IL-33 via TI/ST2L regulates the functions of immune cells including T cells, B cells, DCs, macrophages, mast cells, and innate lymphoid cells (ILCs). Stimulation with IL-33 is crucial for CD4+ T cell polarized into Th2 immunity and for the induction of Treg. CD8+ T cells can also express ST2L and IL-33 promotes features of effector CD8+ T cells. For macrophages and ILCs, ST2L presents on these cells and IL-33 induces Th2 cytokine production. IL-33 modulates adhesion, activation, maturation, and cytokine production by mast cells. ST2 is expressed in B1 and is important for differentiation of IL-10-producing B cells. Understanding the specific role of IL-33/ST2L in different immune cells will help to answer the remaining questions that are important for diseases pathologies and intervention strategies by targeting the IL-33/ST2L signals.

Keywords: IL-33; Immune cells; ST2L; sST2.

Publication types

  • Review

MeSH terms

  • Animals
  • Humans
  • Immune System / cytology*
  • Immune System / physiology*
  • Interleukin-1 Receptor-Like 1 Protein
  • Interleukin-33 / genetics
  • Interleukin-33 / metabolism*
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / metabolism*

Substances

  • IL1RL1 protein, human
  • IL33 protein, human
  • Interleukin-1 Receptor-Like 1 Protein
  • Interleukin-33
  • Receptors, Cell Surface