The immunobiology of prion diseases

Nat Rev Immunol. 2013 Dec;13(12):888-902. doi: 10.1038/nri3553. Epub 2013 Nov 5.

Abstract

Individuals infected with prions succumb to brain damage, and prion infections continue to be inexorably lethal. However, many crucial steps in prion pathogenesis occur in lymphatic organs and precede invasion of the central nervous system. In the past two decades, a great deal has been learnt concerning the cellular and molecular mechanisms of prion lymphoinvasion. These properties are diagnostically useful and have, for example, facilitated preclinical diagnosis of variant Creutzfeldt-Jakob disease in the tonsils. Moreover, the early colonization of lymphoid organs can be exploited for post-exposure prophylaxis of prion infections. As stromal cells of lymphoid organs are crucial for peripheral prion infection, the dedifferentiation of these cells offers a powerful means of hindering prion spread in infected individuals. In this Review, we discuss the current knowledge of the immunobiology of prions with an emphasis on how basic discoveries might enable translational strategies.

Publication types

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

MeSH terms

  • Animals
  • Central Nervous System / pathology
  • Disease Models, Animal
  • Humans
  • Lymphoid Tissue / immunology
  • Lymphoid Tissue / pathology*
  • Mice
  • PrPC Proteins / immunology
  • PrPC Proteins / metabolism
  • PrPSc Proteins / immunology
  • PrPSc Proteins / metabolism
  • Prion Diseases / immunology*
  • Prion Diseases / transmission*
  • Prion Proteins
  • Prions / genetics
  • Prions / immunology
  • Protein Transport

Substances

  • PRNP protein, human
  • PrPC Proteins
  • PrPSc Proteins
  • Prion Proteins
  • Prions