Animal Models for Progressive Multifocal Leukoencephalopathy

J Cell Physiol. 2015 Dec;230(12):2869-74. doi: 10.1002/jcp.25047.

Abstract

Progressive multifocal leukoencephalopathy (PML) is a severe demyelinating disease of the CNS caused by the human polyomavirus JC (JCV). JCV replication occurs only in human cells and investigation of PML has been severely hampered by the lack of an animal model. The common feature of PML is impairment of the immune system. The key to understanding PML is working out the complex mechanisms that underlie viral entry and replication within the CNS and the immunosurveillance that suppresses the virus or allows it to reactivate. Early models involved the simple inoculation of JCV into animals such as monkeys, hamsters, and mice. More recently, mouse models transgenic for the gene encoding the JCV early protein, T-antigen, a protein thought to be involved in the disruption of myelin seen in PML, have been employed. These animal models resulted in tumorigenesis rather than demyelination. Another approach is to use animal polyomaviruses that are closely related to JCV but able to replicate in the animal such as mouse polyomavirus and SV40. More recently, novel models have been developed that involve the engraftment of human cells into the animal. Here, we review progress that has been made to establish an animal model for PML, the advances and limitations of different models and weigh future prospects.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Brain / immunology
  • Brain / metabolism
  • Brain / pathology
  • Brain / virology*
  • Disease Models, Animal
  • Genetic Predisposition to Disease
  • Host-Pathogen Interactions
  • Humans
  • JC Virus / genetics
  • JC Virus / pathogenicity*
  • Leukoencephalopathy, Progressive Multifocal / genetics
  • Leukoencephalopathy, Progressive Multifocal / immunology
  • Leukoencephalopathy, Progressive Multifocal / pathology
  • Leukoencephalopathy, Progressive Multifocal / virology*
  • Myelin Sheath / metabolism
  • Phenotype
  • Species Specificity
  • Virus Replication