Elevated expression of interleukin-33 in myasthenia gravis patients

J Clin Neurosci. 2019 May:63:32-36. doi: 10.1016/j.jocn.2019.02.012. Epub 2019 Mar 1.

Abstract

Myasthenia gravis (MG) is an archetypal autoimmune disorder of the neuromuscular junction. The imbalance of inflammatory cytokines are involved in the pathogenesis of MG. IL-33, a member of the IL-1 family, plays a key immune-modulation role in several autoimmune disease. However, its regulatory role in MG remains unclear. Here, we demonstrated that IL-33 expression in the serum of MG patients was significantly increased. We further proved that the serum levels of IL-33 were significantly negative correlated with the expression levels of TSLP. Increased serum IL-33 levels positively correlated with the upregulation of IL-17A levels and the quantitative myasthenia gravis (QMG) score in MG patients. Our findings indicate that IL-33 plays a potent immuno- enhancing role in the pathogenesis of MG by downregulating TSLP, consequently affecting the development of Th17 cells in MG.

Keywords: IL-33; Myasthenia gravis; TSLP; Th17 cells.

MeSH terms

  • Biomarkers / blood
  • Female
  • Humans
  • Interleukin-33 / blood*
  • Male
  • Middle Aged
  • Myasthenia Gravis / blood*
  • Th17 Cells / immunology

Substances

  • Biomarkers
  • IL33 protein, human
  • Interleukin-33