Psoriasis Plays a Wild CARD

J Invest Dermatol. 2018 Sep;138(9):1903-1905. doi: 10.1016/j.jid.2018.05.001.

Abstract

Rare autosomal mutations in CARD14 have previously been linked to psoriasis susceptibility in humans, but their pathogenic role had not been shown. Mellett et al. generated mice harboring the patient-derived gain-of-function Card14ΔE138 mutation and showed that hyperactivation of CARD14 alone is sufficient to induce immunopathogenic mechanisms that are responsible for psoriasis, which is driven by the IL-17/IL-23 axis.

Publication types

  • Comment

MeSH terms

  • Animals
  • CARD Signaling Adaptor Proteins / genetics
  • Gain of Function Mutation
  • Guanylate Cyclase / genetics
  • Humans
  • Inflammation
  • Interleukin-17*
  • Interleukin-23
  • Membrane Proteins / genetics
  • Mice
  • Mutation
  • NF-kappa B / genetics
  • Psoriasis*

Substances

  • CARD Signaling Adaptor Proteins
  • Interleukin-17
  • Interleukin-23
  • Membrane Proteins
  • NF-kappa B
  • CARD14 protein, human
  • Guanylate Cyclase