Atypical inflammation in the central nervous system in prion disease

Curr Opin Neurol. 2002 Jun;15(3):349-54. doi: 10.1097/00019052-200206000-00020.

Abstract

The inflammatory response in prion diseases is dominated by microglial activation. Contrary to their profile in vitro none of the pro-inflammatory cytokines interleukin-1beta, interleukin-6, or tumour necrosis factor-alpha are significantly upregulated in the ME7 model of prion disease. However, two major inflammatory mediators are elevated: transforming growth factor-beta1 and prostaglandin E2. This cytokine profile is the same as that reported for macrophages during phagocytosis of apoptotic cells and indeed transforming growth factor-beta1 and prostaglandin E2 are responsible for the downregulated phenotype of these macrophages. Transforming growth factor-beta1 may also have roles in extracellular matrix deposition and in amyloidogenesis and may play a direct role in disease pathogenesis. There is also now evidence to suggest that a peripheral infection, and its consequent systemic cytokine expression, may drive central nervous system cytokine expression and perhaps exacerbate disease.

Publication types

  • Review

MeSH terms

  • Animals
  • Central Nervous System / immunology*
  • Central Nervous System / metabolism
  • Central Nervous System / physiopathology
  • Cytokines / immunology*
  • Cytokines / metabolism
  • Dinoprostone / immunology
  • Encephalitis / immunology*
  • Encephalitis / metabolism
  • Encephalitis / physiopathology
  • Humans
  • Microglia / cytology
  • Microglia / immunology*
  • Microglia / metabolism
  • Prion Diseases / immunology*
  • Prion Diseases / metabolism
  • Prion Diseases / physiopathology
  • Reactive Oxygen Species / immunology
  • Transforming Growth Factor beta / immunology

Substances

  • Cytokines
  • Reactive Oxygen Species
  • Transforming Growth Factor beta
  • Dinoprostone