Effect of high-dose vitamin D supplementation on antibody responses against Epstein-Barr virus in relapsing-remitting multiple sclerosis.

Egil Røsjø, Andreas Lossius, Nada Abdelmagid, Jonas C Lindstrøm, Margitta T Kampman, Lone Jørgensen, Peter Sundström, Tomas Olsson, Linn H Steffensen, Øivind Torkildsen, Trygve Holmøy

Journal: Multiple sclerosis (Houndmills, Basingstoke, England) 2018;23(3):395-402

PMID: 27325604

Abstract

BACKGROUND

Elevated antibody levels against Epstein-Barr virus (EBV) and a poor vitamin D status are environmental factors that may interact in relapsing-remitting multiple sclerosis (RRMS) aetiology.

OBJECTIVES

To examine effects of high-dose oral vitamin D supplementation on antibody levels against EBV nuclear antigen 1 (EBNA1) in RRMS.

METHODS

Serum 25-hydroxyvitamin D (25(OH)D) and immunoglobulin G antibody levels against EBNA1 (whole protein and amino acid 385-420 fragment), EBV viral capsid antigen (VCA), cytomegalovirus (CMV) and varicella zoster virus (VZV) were measured in 68 RRMS patients enrolled in a 96-week randomised double-blinded placebo-controlled clinical trial of oral vitamin D supplementation (20,000 IU/week) (NCT00785473).

RESULTS

The mean 25(OH)D level more than doubled in the vitamin D group and was significantly higher than in the placebo group at study conclusion (123.2 versus 61.8 nmol/L, p < 0.001). Compared to the placebo group, both anti-EBNA1 protein and fragment antibody levels decreased in the vitamin D group from baseline to week 48 ( p = 0.038 and p = 0.004, respectively), but not from baseline to week 96. Vitamin D supplementation did not affect antibodies against VCA, CMV or VZV.

CONCLUSION

The results indicate that high-dose oral vitamin D supplementation can affect humoral immune responses against the latent EBV antigen EBNA1 in RRMS.

Address: Department of Neurology, Akershus University Hospital, Lørenskog, Norway/Institute of Clinical Medicine, University of Oslo, Oslo, Norway.; Institute of Clinical Medicine, University of Oslo, Oslo, Norway/Department of Immunology and Transfusion Medicine, Oslo University Hospital Rikshospitalet, Oslo, Norway.; Department of Clinical Neuroscience, Neuroimmunology Unit, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.; Institute of Clinical Medicine, University of Oslo, Oslo, Norway/Helse Øst Health Services Research Centre, Akershus University Hospital, Lørenskog, Norway.; Department of Neurology, University Hospital of North Norway, Tromsø, Norway.; Department of Health and Care Sciences, University of Tromsø, Tromsø, Norway/Department of Clinical Therapeutic Services, University Hospital of North Norway, Tromsø, Norway.; Department of Pharmacology and Clinical Neuroscience, Section of Neurology, Umeå University, Umeå, Sweden.; Department of Neurology, University Hospital of North Norway, Tromsø, Norway/Department of Clinical Medicine, University of Tromsø, Tromsø, Norway.; KG Jebsen MS Research Centre, Department of Clinical Medicine, University of Bergen, Bergen, Norway/Norwegian Multiple Sclerosis Competence Centre, Department of Neurology, Haukeland University Hospital, Bergen, Norway.

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