Challenges and directions for the pathogen hypothesis of Alzheimer's disease

Neurobiol Aging. May-Jun 2004;25(5):629-37. doi: 10.1016/j.neurobiolaging.2003.12.022.

Abstract

This paper critically reviews the possibility that infiltration of the brain by pathogens (e.g. Herpes simplex virus type 1 (HSV1) or Chlamydophila pneumoniae (Cp)) acts as a trigger or co-factor for Alzheimer's disease (AD). The evidence currently available is limited and in some cases inconsistent, but it does justify the need for more vigorous investigation of this hypothesis. An issue of particular concern is the paucity of experimental evidence showing that pathogens can elicit the neuropathological changes and cognitive deficits that characterise AD. Other weaknesses include a failure to obtain independent confirmation of Cp in AD brains, and a lack of evidence for HSV1 proteins or intact virions in AD brain tissue. Future avenues of investigation that might prove fruitful include epidemiological investigations of the incidence of AD in individuals who are either immunosuppressed or have received chronic antiviral or antibiotic therapy. There is also a need to consider systemic infections as potential contributors to the pathogenesis of AD.

Publication types

  • Review

MeSH terms

  • Alzheimer Disease / etiology*
  • Alzheimer Disease / microbiology
  • Alzheimer Disease / virology
  • Animals
  • Brain Diseases / complications*
  • Brain Diseases / microbiology
  • Brain Diseases / virology
  • Chlamydia Infections / complications
  • Chlamydophila pneumoniae / pathogenicity*
  • Encephalitis, Herpes Simplex / complications
  • Herpesvirus 1, Human / pathogenicity*
  • Humans
  • Risk Factors