Biochemically altered myelin triggers autoimmune demyelination

Proc Natl Acad Sci U S A. 2018 May 22;115(21):5528-5533. doi: 10.1073/pnas.1721115115. Epub 2018 May 4.

Abstract

Although immune attack against central nervous system (CNS) myelin is a central feature of multiple sclerosis (MS), its root cause is unresolved. In this report, we provide direct evidence that subtle biochemical modifications to brain myelin elicit pathological immune responses with radiological and histological properties similar to MS lesions. A subtle myelinopathy induced by abbreviated cuprizone treatment, coupled with subsequent immune stimulation, resulted in lesions of inflammatory demyelination. The degree of myelin injury dictated the resulting immune response; biochemical damage that was too limited or too extensive failed to trigger overt pathology. An inhibitor of peptidyl arginine deiminases (PADs), enzymes that alter myelin structure and correlate with MS lesion severity, mitigated pathology even when administered only during the myelin-altering phase. Moreover, cultured splenocytes were reactive against donor myelin isolates, a response that was substantially muted when splenocytes were exposed to myelin from donors treated with PAD inhibitors. By showing that a primary biochemical myelinopathy can trigger secondary pathological inflammation, "cuprizone autoimmune encephalitis" potentially reconciles conflicting theories about MS pathogenesis and provides a strong rationale for investigating myelin as a primary target for early, preventative therapy.

Keywords: citrullination; cuprizone; immunopathogenesis; multiple sclerosis; myelin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cuprizone / toxicity
  • Demyelinating Diseases / etiology*
  • Demyelinating Diseases / pathology
  • Disease Models, Animal*
  • Encephalitis / chemically induced
  • Encephalitis / immunology
  • Encephalitis / pathology*
  • Hashimoto Disease / chemically induced
  • Hashimoto Disease / immunology
  • Hashimoto Disease / pathology*
  • Humans
  • Hydrolases / genetics
  • Hydrolases / metabolism
  • Inflammation / chemically induced
  • Inflammation / immunology
  • Inflammation / pathology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Monoamine Oxidase Inhibitors / toxicity
  • Multiple Sclerosis / etiology*
  • Multiple Sclerosis / pathology
  • Myelin Sheath / immunology
  • Myelin Sheath / metabolism
  • Myelin Sheath / pathology*

Substances

  • Monoamine Oxidase Inhibitors
  • Cuprizone
  • Hydrolases
  • arginine deiminase

Supplementary concepts

  • Hashimoto's encephalitis