IL-17A is associated with the breakdown of the blood-brain barrier in relapsing-remitting multiple sclerosis

J Neuroimmunol. 2019 Jul 15:332:147-154. doi: 10.1016/j.jneuroim.2019.04.011. Epub 2019 Apr 21.

Abstract

IL-17 has been implicated in the pathogenesis of multiple sclerosis (MS). Here, we show that blockade of IL-17A, but not IL-17F, attenuated experimental autoimmune encephalomyelitis (EAE). We further show that IL-17A levels were elevated in the CSF of relapsing-remitting MS (RRMS) patients and that they correlated with the CSF/serum albumin quotient (Qalb), a measure of blood-brain barrier (BBB) dysfunction. We then demonstrated that the combination of IL-17A and IL-6 reduced the expression of tight junction (TJ)-associated genes and disrupted monolayer integrity in the BBB cell line hCMEC/D3. However, unlike IL-17A, IL-6 in the CSF from RRMS patients did not correlate with Qalb. These data highlight the potential importance of targeting IL-17A in preserving BBB integrity in RRMS.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Animals
  • Blood-Brain Barrier*
  • Cells, Cultured
  • Encephalomyelitis, Autoimmune, Experimental / physiopathology*
  • Encephalomyelitis, Autoimmune, Experimental / therapy
  • Endothelial Cells / drug effects
  • Endothelial Cells / metabolism
  • Female
  • Humans
  • Immunization, Passive
  • Interleukin-17 / antagonists & inhibitors
  • Interleukin-17 / cerebrospinal fluid
  • Interleukin-17 / physiology*
  • Interleukin-6 / pharmacology
  • Mice
  • Mice, Inbred C57BL
  • Middle Aged
  • Multiple Sclerosis, Relapsing-Remitting / cerebrospinal fluid
  • Multiple Sclerosis, Relapsing-Remitting / physiopathology*
  • Receptors, Interleukin-6 / physiology
  • Recombinant Proteins / pharmacology
  • Young Adult

Substances

  • IL17A protein, human
  • IL17F protein, human
  • IL6 protein, human
  • Il17a protein, mouse
  • Interleukin-17
  • Interleukin-6
  • Receptors, Interleukin-6
  • Recombinant Proteins