Distribution and quantification of human herpesvirus 6 in multiple sclerosis and control brains

P W Tuke1, S Hawke, P D Griffiths

  • 1Centre for Virology, Department of Infection, Royal Free and University College Medical School of UCL, Hampstead Site, Rowland Hill Street, London NW3 2PF, UK.

Multiple Sclerosis (Houndmills, Basingstoke, England)
|August 26, 2004
PubMed

Insights

Human herpesvirus 6 (HHV-6) DNA was detected in brains of multiple sclerosis (MS) patients and controls at similar levels. This study found no significant differences in HHV-6 presence, variant, or quantity in MS brains, suggesting it may not be a key factor.

Area of Science:

  • Neurovirology
  • Immunology
  • Pathology

Background:

  • Multiple sclerosis (MS) is an autoimmune disease with suspected environmental triggers.
  • Human herpesvirus 6 (HHV-6) has been implicated as a potential environmental factor in MS pathogenesis.
  • Understanding the role of viruses like HHV-6 in MS is crucial for disease etiology and treatment.

Purpose of the Study:

  • To investigate the presence, variant type, and quantity of HHV-6 DNA in post-mortem brain samples from MS patients and controls.
  • To determine if HHV-6 distribution or load differs between MS cases and healthy controls.
  • To assess HHV-6 presence in both normal-appearing and lesional brain tissue in MS.

Main Methods:

  • Post-mortem brain tissue samples from 124 individuals (MS cases and controls) were analyzed.
  • Seven anatomically defined brain regions were tested for HHV-6 DNA using Polymerase Chain Reaction (PCR).
  • Viral load was quantified, and HHV-6 variants were identified.

Main Results:

  • HHV-6 DNA was detected in 41% of MS cases and 44% of control samples.
  • Median viral loads were comparable between MS cases (11 genome copies/µg DNA) and controls (9 genome copies/µg DNA).
  • No significant differences in HHV-6 distribution, variant type (predominantly variant B), or quantity were found between MS brains and controls, or in lesional versus normal-appearing tissue.

Conclusions:

  • These findings confirm the neurotropic nature of HHV-6.
  • The study does not support a significant role for HHV-6 in the pathogenesis of multiple sclerosis based on its presence, variant, or quantity in the brain.
  • Further research may be needed to explore other potential environmental factors or mechanisms in MS etiology.