The DNA copy number of human endogenous retrovirus-W (MSRV-type) is increased in multiple sclerosis patients and is influenced by gender and disease severity

PLoS One. 2013;8(1):e53623. doi: 10.1371/journal.pone.0053623. Epub 2013 Jan 7.

Abstract

Background: Multiple sclerosis is an autoimmune disease more prevalent in women than in men. Multiple Sclerosis Associated Retrovirus element (MSRV) is a member of type-W endogenous retrovirus family (HERV-W), known to be associated to MS. Most HERVs are unable to replicate but MSRV expression associated with reverse-transcriptase activity in MS would explain reported DNA copy number increase in MS patients. A potential link between HERV-W copies on chromosome X and gender differential prevalence has been suggested. The present study addresses MSRV-type DNA load in relation with the gender differences and clinical status in MS and healthy controls.

Results: 178 MS patients (62.9% women) and 124 controls (56.5% women) were included. MSRV env load (copies/pg of DNA) was analyzed by real time qPCR with specific primers and probe for its env gene, in DNA from peripheral blood mononuclear cells (PBMCs). MSRV load was more elevated in MS patients than in controls (p = 4.15e-7). MS women presented higher MSRV load than control women (p = 0.009) and MS men also had higher load than control men (p = 2.77e-6). Besides, women had higher levels than men, both among patients (p = 0.007) and controls (p = 1.24e-6). Concordantly, EDSS and MSSS scores were higher among female patients with an elevated MSRV load (p = 0.03 and p = 0.04, respectively).

Conclusions: MSRV increases its copy number in PBMC of MS patients and particularly in women with high clinical scores. This may explain causes underlying the higher prevalence of MS in women. The association with the clinical severity calls for further investigations on MSRV load in PBMCs as a biomarker for MS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Chromosomes, Human, X / virology
  • DNA Copy Number Variations*
  • DNA, Viral / genetics*
  • Endogenous Retroviruses / genetics*
  • Female
  • Genes, env*
  • Humans
  • Leukocytes, Mononuclear / metabolism
  • Leukocytes, Mononuclear / virology
  • Male
  • Middle Aged
  • Multiple Sclerosis / genetics*
  • Multiple Sclerosis / pathology*
  • Real-Time Polymerase Chain Reaction
  • Severity of Illness Index
  • Sex Factors
  • Viral Load

Substances

  • DNA, Viral

Grants and funding

MGM, MDM and AAL are recipients of a contract of “Fundación para la Investigación Biomédica-Hospital Clínico San Carlos”. RAL is recipient of a research contract of the Instituto de Salud Carlos III-Fondo Europeo de Desarrollo Regional (Feder) (CP07/00273). AGM is recipient of a technician contract from “REEM: Red Española de Esclerosis Múltiple” (RETICS-REEM RD07/0060; www.reem.es.) This work was supported by Geneuro and by grants from: Instituto de Salud Carlos III-Fondo Investigaciones Sanitarias FIS (09/02074), “Fundación Mutua Madrileña”, and “Fundación LAIR”. All of the funders but Geneuro had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.