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   <subfield code="a">10.1177/1352458517722646</subfield>
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   <subfield code="a">Exploring the effect of vitamin D&lt;sub&gt;3&lt;/sub&gt; supplementation on the anti-EBV antibody response in relapsing-remitting multiple sclerosis</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[L. Rolf, A.H. Muris, A. Mathias, R. Du Pasquier, I. Koneczny, G. Disanto, J. Kuhle, S. Ramagopalan, J. Damoiseaux, J. Smolders, R. Hupperts]</subfield>
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   <subfield code="a">Epstein-Barr virus (EBV) infection and vitamin D insufficiency are potentially interacting risk factors for multiple sclerosis (MS). To investigate the effect of high-dose vitamin D &amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; supplements on antibody levels against the EBV nuclear antigen-1 (EBNA-1) in patients with relapsing-remitting multiple sclerosis (RRMS) and to explore any underlying mechanism affecting anti-EBNA-1 antibody levels. This study utilized blood samples from a randomized controlled trial in RRMS patients receiving either vitamin D &amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; (14,000 IU/day; n = 30) or placebo ( n = 23) over 48 weeks. Circulating levels of 25-hydroxyvitamin-D, and anti-EBNA-1, anti-EBV viral capsid antigen (VCA), and anti-cytomegalovirus (CMV) antibodies were measured. EBV load in leukocytes, EBV-specific cytotoxic T-cell responses, and anti-EBNA-1 antibody production in vitro were also explored. The median antibody levels against EBNA-1, but not VCA and CMV, significantly reduced in the vitamin D &amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; group (526 (368-1683) to 455 (380-1148) U/mL) compared to the placebo group (432 (351-1280) to 429 (297-1290) U/mL; p = 0.023). EBV load and cytotoxic T-cell responses were unaffected. Anti-EBNA-1 antibody levels remained below detection limits in B-cell cultures. High-dose vitamin D &amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; supplementation selectively reduces anti-EBNA-1 antibody levels in RRMS patients. Our exploratory studies do not implicate a promoted immune response against EBV as the underlying mechanism.</subfield>
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