4.7 Article

Anti-JC virus antibodies in a large German natalizumab-treated multiple sclerosis cohort

Journal

NEUROLOGY
Volume 78, Issue 22, Pages 1736-1742

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0b013e3182583022

Keywords

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Funding

  1. German Bundesministerium fur Bildung und Forschung (BMBF), German competence Network Multiple Sclerosis (KKNMS) [01GI0914]
  2. Biogen Idec
  3. Bayer Schering
  4. Teva-sanofi aventis
  5. Merck Serono
  6. Novartis Pharma
  7. German Ministry for Education and Research (BMBF, German Competence Network Multiple Sclerosis)
  8. Bayer Healthcare
  9. Biogen Idec/Elan
  10. sanofi-aventis
  11. Schering-Plough Corp.
  12. EMD Serono
  13. TEVA Neuroscience
  14. Medac
  15. Lundbeck Research USA Inc.
  16. Novo Nordisk
  17. Novartis

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Objective: To investigate the rate of seropositivity of anti-JC virus (JCV) antibodies in a German multiple sclerosis (MS) cohort treated with natalizumab in the postmarketing setting and to assess anti-JCV serostatus in samples obtained before diagnosis of progressive multifocal leukoencephalopathy (PML). Methods: This was a blinded, retrospective cross-sectional and longitudinal analysis for anti-JCV antibodies using a confirmatory 2-step ELISA on 2,782 blood samples obtained from 2,253 patients nationwide for routine testing for anti-natalizumab antibodies during open-label treatment between 2007 and 2010. Results: Of the natalizumab-treated patients with MS, 58.8% tested positive for anti-JCV antibodies. The rate of seropositivity was higher in males and increased with age, with a plateau between age intervals 20-29 and 30-39 years. In longitudinal analyses, 19 of 194 (9.8%) patients converted from anti-JCV antibody-negative to seropositive status over 7.7 months; 4.7% reverted from antibody-positive to seronegative status over 7.9 months. Antibody levels, especially in the latter group, were low, indicating fluctuations around the lower cut point of the assay. Neither anti-JCV serostatus nor antibody levels were associated with immunosuppressive pretreatment, duration of natalizumab treatment, or anti-natalizumab antibodies. All samples obtained from 10 patients who developed PML were seropositive (13 samples before PML diagnosis [2.0-37.6 months]; 2 samples at diagnosis). Antibody levels in these samples were higher than those in samples from seropositive patients who did not develop PML. Conclusions: These data argue for the potential clinical utility of JCV serology for PML risk stratification. However, further investigations of fluctuations in serostatus and of antibody levels for a more precise understanding of the predictive value are warranted. Neurology (R) 2012;78:1736-1742

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