Inflammatory responses in Multiple Sclerosis normal-appearing white matter and in non-immune mediated neurological conditions with wallerian axonal degeneration: A comparative study

J Neuroimmunol. 2017 Nov 15:312:49-58. doi: 10.1016/j.jneuroim.2017.09.004. Epub 2017 Sep 8.

Abstract

Inflammatory-like changes in the white matter (WM) are commonly observed in conditions of axonal degeneration by different etiologies. This study is a systematic comparison of the principal features of the inflammatory-like changes in the WM in different pathological conditions characterized by axonal damage/degeneration, focusing in particular on Multiple Sclerosis (MS) normal-appearing white matter (NAWM) compared to non immune-mediated disorders. The study was performed on sections of NAWM from 15 MS cases, 11 cases of non immune-mediated disorders with wallerian axonal degeneration (stroke, trauma, amyotrophic lateral sclerosis), 3 cases of viral encephalitis, 6 control cases. Common features of the inflammatory-like changes observed in all of the conditions of WM pathology were diffuse endothelial expression of VCAM-1, microglial activation with expression of M2 markers, increased expression of sphingosine receptors. Inflammation in MS NAWM was characterized, compared to non immune-mediated conditions, by higher VCAM-1 expression, higher density of perivascular lymphocytes, focal perivascular inflammation with microglial expression of M1 markers, ongoing acute axonal damage correlating with VCAM-1 expression but not with microglia activation. Inflammatory changes in MS NAWM share all the main features observed in the WM in non immune-mediated conditions with wallerian axonal degeneration (with differences to a large extent more quantitative than qualitative), but with superimposition of disease-specific perivascular inflammation and ongoing acute axonal damage.

Keywords: Axon; Inflammation; Microglia; Multiple Sclerosis (MS); Normal-appearing white matter (NAWM); S1P1; Sphingosine; VCAM-1; Wallerian degeneration.

MeSH terms

  • Adult
  • Aged
  • Antigens, CD / metabolism
  • Blood-Brain Barrier / physiopathology
  • Encephalitis, Viral / metabolism
  • Encephalitis, Viral / pathology
  • Endothelium / metabolism
  • Endothelium / pathology
  • Female
  • Humans
  • Inflammation / etiology*
  • Lymphocytes / metabolism
  • Lymphocytes / pathology
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Multiple Sclerosis / complications*
  • Multiple Sclerosis / pathology
  • Nitric Oxide Synthase Type II / metabolism
  • Vascular Cell Adhesion Molecule-1 / metabolism
  • Wallerian Degeneration / complications*
  • Wallerian Degeneration / pathology
  • White Matter / diagnostic imaging
  • White Matter / pathology*

Substances

  • Antigens, CD
  • Vascular Cell Adhesion Molecule-1
  • Nitric Oxide Synthase Type II