4.5 Article

Epstein-Barr virus and multiple sclerosis: interaction with HLA

Journal

GENES AND IMMUNITY
Volume 13, Issue 1, Pages 14-20

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/gene.2011.42

Keywords

multiple sclerosis; Epstein-Barr virus; HLA; interactions; case-control study

Funding

  1. Swedish Association for Persons with Neurological Disabilities
  2. BiogenIdec
  3. MerckSerono
  4. Bayer Schering
  5. Swedish Medical Research Council [Dnr 521-2009-2596]
  6. Swedish Council for Working life and Social Research [Dnr 2009-0650]
  7. Bayer
  8. SanofiAventis
  9. Merck
  10. AFA foundation
  11. Swedish Foundation for Working Life and Social research
  12. FP6 program Neuropromise [LSHM-CT-2005-018637]

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Epstein-Barr virus (EBV) infection, history of infectious mononucleosis (IM) and HLA-A and DRB1 have all been proposed as risk factors for multiple sclerosis (MS). Our aim was to analyse possible interactions between antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA1) or EBNA1 fragments, presence of DRB1*15 and absence of A*02. The study population includes newly diagnosed cases and matched controls. Interaction on the additive scale was calculated using attributable proportion due to interaction (AP), which is the proportion of the incidence among individuals exposed to two interacting factors that is attributable to the interaction per se. IM showed association with MS, odds ratio (OR) = 1.89 (1.45-2.48% confidence interval (Cl)), as did raised EBNA1 IgG OR = 1.74 (1.38-2.18 95%CI). All EBNA1 fragment IgGs were associated with MS risk. However, EBNA1 fragment 385-420 IgG levels were more strongly associated to MS than total EBNA1 IgG, OR = 3.60 (2.75-4.72 95%CI), and also interacted with both DRB1*15 and absence of A*02, AP 0.60 (0.45-0.76 95%CI) and AP 0.39 (0.18-0.61 95%CI), respectively. The observed interaction between HLA class I and 11 genotype and reactivity to EBV-related epitopes suggest that the mechanism through which HLA genes influence the risk of MS may, at least in part, involve the immune control of EBV infection. Genes and Immunity (2012) 13, 14-20; doi:10.1038/gene.2011.42; published online 21 July 2011

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