TY - JOUR
T1 - Anti-JC virus antibodies in a large German natalizumab-treated multiple sclerosis cohort
AU - Trampe, A. K.
AU - Hemmelmann, C.
AU - Stroet, A.
AU - Haghikia, A.
AU - Hellwig, K.
AU - Wiendl, H.
AU - Goelz, S.
AU - Ziegler, A.
AU - Gold, R.
AU - Chan, A.
N1 - Funding Information:
Study funding: Supported in part by the German Bundesministerium für Bildung und Forschung (BMBF), German competence Network Multiple Sclerosis (KKNMS), natalizumab pharmacovigilance study no. 01GI0914. Biogen Idec provided financial support for shipment and analysis of samples.
Funding Information:
A.K. Trampe and Dr. Hemmelmann report no disclosures. Dr. Stroet has received personal compensation for activities with Novartis. Dr. Haghikia has received limited research support from Biogen Idec and speaker honoraria from Bayer Healthcare, Biogen Idec, Teva, and Merck Serono. Dr. Hellwig had received research support and speaker honoraria from Biogen Idec, Bayer Schering, Teva-sanofi aventis, Merck Serono, and Novartis Pharma. Dr. Wiendl has received research support from the German Ministry for Education and Research (BMBF, “German Competence Network Multiple Sclerosis”), Bayer Healthcare, Biogen Idec/Elan, sanofi-aventis, Schering-Plough Corp., EMD Serono, TEVA Neuroscience, Medac, Lundbeck Research USA Inc., and Novo Nordisk and personal compensation for activities with Bayer Healthcare, Biogen Idec/Elan, sanofi-aventis, Schering-Plough Corp., EMD Serono, TEVA Neuroscience, Medac, Lundbeck Research USA Inc., and Novo Nordisk as a speaker or consultant. Dr. Goelz was an employee of Biogen Idec and is an employee of Elan Pharmaceuticals and holds stock. Dr. Ziegler has received research support from the German Ministry for Education and Research (BMBF, “German Competence Network Multiple Sclerosis”). Dr. Gold has received personal compensation for activities with Bayer Healthcare, Biogen Idec, and Teva Neuroscience and in an editorial capacity from Therapeutic Advances in Neurological Disorders; patent payments from Biogen Idec, and research support from the German Ministry for Education and Research (BMBF, “German Competence Network Multiple Sclerosis” [KKNMS], CONTROL MS, 01GI0914), Bayer Healthcare, Biogen Idec, Merck Serono, Teva Neuroscience, and Novartis. Dr. Chan has received personal compensation as a speaker or consultant for Bayer Schering, Biogen Idec, Merck Serono, Novartis, sanofi-aventis, and Teva Neuroscience and research support from the German Ministry for Education and Research (BMBF, “German Competence Network Multiple Sclerosis” [KKNMS], CONTROL MS, 01GI0914), Bayer Schering, Biogen Idec, Merck Serono, and Novartis. Go to Neurology.org for full disclosures .
PY - 2012/5/29
Y1 - 2012/5/29
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84863607194&partnerID=8YFLogxK
U2 - 10.1212/WNL.0b013e3182583022
DO - 10.1212/WNL.0b013e3182583022
M3 - Journal articles
AN - SCOPUS:84863607194
SN - 0028-3878
VL - 78
SP - 1736
EP - 1742
JO - Neurology
JF - Neurology
IS - 22
ER -