IL-12 and IL-23/Th17 axis in systemic lupus erythematosus

Exp Biol Med (Maywood). 2019 Jan;244(1):42-51. doi: 10.1177/1535370218824547. Epub 2019 Jan 21.

Abstract

Our article is focused on emerging pathogenetic pathways in systemic lupus erythematosus (SLE). Notably, IL-12 and IL-23 have been described as emerging cytokines in SLE pathogenesis. We know that IL-23 stimulates Th17 cells to produce IL-17. We try to point out the importance of IL-23/Th17 axis in SLE and to focus on the interaction between this axis and IL-12. Ustekinumab, a fully human IgG1κ monoclonal antibody directed towards the p40 shared subunit of IL-12 and IL-23, has been recently investigated in SLE, suggesting a potential novel therapeutic strategy in SLE. To our knowledge, there are no reviews which simultaneously focus on IL-12 an IL-23/Th17 axis in SLE. Thus, we believe our work will be of interest to the readers.

Keywords: IL-12; IL-23/Th17 axis; SLE; Th1 response; immune response; ustekinumab.

Publication types

  • Review

MeSH terms

  • Animals
  • Antibodies, Monoclonal / therapeutic use
  • Humans
  • Interleukin-12 / blood
  • Interleukin-12 / physiology*
  • Interleukin-23 / blood
  • Interleukin-23 / physiology*
  • Lupus Erythematosus, Systemic / drug therapy
  • Lupus Erythematosus, Systemic / immunology*
  • Lupus Erythematosus, Systemic / metabolism
  • Mice
  • Th17 Cells / immunology*
  • Ustekinumab / therapeutic use

Substances

  • Antibodies, Monoclonal
  • Interleukin-23
  • Interleukin-12
  • Ustekinumab