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Impact of Disease-Modifying Treatments on the Longitudinal Evolution of Anti-JCV Antibody Index in Multiple Sclerosis

Background: Risk of natalizumab-related progressive multifocal leukoencephalopathy is associated with the presence of anti-JC-virus (JCV) antibodies. Objective: To investigate the impact of disease-modifying treatments (DMT) on the longitudinal evolution of anti-JCV antibody index. Methods: Patients...

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Autores principales: Hegen, Harald, Walde, Janette, Bsteh, Gabriel, Auer, Michael, Wurth, Sebastian, Zinganell, Anne, Di Pauli, Franziska, Deisenhammer, Florian, Berger, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209669/
https://www.ncbi.nlm.nih.gov/pubmed/30410486
http://dx.doi.org/10.3389/fimmu.2018.02435
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author Hegen, Harald
Walde, Janette
Bsteh, Gabriel
Auer, Michael
Wurth, Sebastian
Zinganell, Anne
Di Pauli, Franziska
Deisenhammer, Florian
Berger, Thomas
author_facet Hegen, Harald
Walde, Janette
Bsteh, Gabriel
Auer, Michael
Wurth, Sebastian
Zinganell, Anne
Di Pauli, Franziska
Deisenhammer, Florian
Berger, Thomas
author_sort Hegen, Harald
collection PubMed
description Background: Risk of natalizumab-related progressive multifocal leukoencephalopathy is associated with the presence of anti-JC-virus (JCV) antibodies. Objective: To investigate the impact of disease-modifying treatments (DMT) on the longitudinal evolution of anti-JCV antibody index. Methods: Patients with multiple sclerosis who had serum sampling at intervals of 6 ± 3 months over up to 6 years and who either started DMT (interferon-β, glatiramer acetate or natalizumab) during the observation period with at least one serum sample available before and after treatment initiation or received no DMT during the observation period were included. Anti-JCV antibody serological status and index were determined by 2-step second-generation anti-JCV antibody assay. Results: A total of 89 patients were followed for a median time of 55.2 months. Of those, 62 (69.7%) started DMT and 27 (30.3%) were without therapy during the observation period. Variation of longitudinal anti-JCV antibody index ranged from 9 to 15% and was similar in patients with and without DMT. Applying a mixed model considering the combined effects of treatment and time as well as individual heterogeneity did not show a significant change of anti-JCV antibody index by the start of treatment with interferon-β, glatiramer acetate, or natalizumab. Conclusion: Evaluated DMTs do not impact longitudinal anti-JCV antibody index evolution.
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spelling pubmed-62096692018-11-08 Impact of Disease-Modifying Treatments on the Longitudinal Evolution of Anti-JCV Antibody Index in Multiple Sclerosis Hegen, Harald Walde, Janette Bsteh, Gabriel Auer, Michael Wurth, Sebastian Zinganell, Anne Di Pauli, Franziska Deisenhammer, Florian Berger, Thomas Front Immunol Immunology Background: Risk of natalizumab-related progressive multifocal leukoencephalopathy is associated with the presence of anti-JC-virus (JCV) antibodies. Objective: To investigate the impact of disease-modifying treatments (DMT) on the longitudinal evolution of anti-JCV antibody index. Methods: Patients with multiple sclerosis who had serum sampling at intervals of 6 ± 3 months over up to 6 years and who either started DMT (interferon-β, glatiramer acetate or natalizumab) during the observation period with at least one serum sample available before and after treatment initiation or received no DMT during the observation period were included. Anti-JCV antibody serological status and index were determined by 2-step second-generation anti-JCV antibody assay. Results: A total of 89 patients were followed for a median time of 55.2 months. Of those, 62 (69.7%) started DMT and 27 (30.3%) were without therapy during the observation period. Variation of longitudinal anti-JCV antibody index ranged from 9 to 15% and was similar in patients with and without DMT. Applying a mixed model considering the combined effects of treatment and time as well as individual heterogeneity did not show a significant change of anti-JCV antibody index by the start of treatment with interferon-β, glatiramer acetate, or natalizumab. Conclusion: Evaluated DMTs do not impact longitudinal anti-JCV antibody index evolution. Frontiers Media S.A. 2018-10-25 /pmc/articles/PMC6209669/ /pubmed/30410486 http://dx.doi.org/10.3389/fimmu.2018.02435 Text en Copyright © 2018 Hegen, Walde, Bsteh, Auer, Wurth, Zinganell, Di Pauli, Deisenhammer and Berger. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Hegen, Harald
Walde, Janette
Bsteh, Gabriel
Auer, Michael
Wurth, Sebastian
Zinganell, Anne
Di Pauli, Franziska
Deisenhammer, Florian
Berger, Thomas
Impact of Disease-Modifying Treatments on the Longitudinal Evolution of Anti-JCV Antibody Index in Multiple Sclerosis
title Impact of Disease-Modifying Treatments on the Longitudinal Evolution of Anti-JCV Antibody Index in Multiple Sclerosis
title_full Impact of Disease-Modifying Treatments on the Longitudinal Evolution of Anti-JCV Antibody Index in Multiple Sclerosis
title_fullStr Impact of Disease-Modifying Treatments on the Longitudinal Evolution of Anti-JCV Antibody Index in Multiple Sclerosis
title_full_unstemmed Impact of Disease-Modifying Treatments on the Longitudinal Evolution of Anti-JCV Antibody Index in Multiple Sclerosis
title_short Impact of Disease-Modifying Treatments on the Longitudinal Evolution of Anti-JCV Antibody Index in Multiple Sclerosis
title_sort impact of disease-modifying treatments on the longitudinal evolution of anti-jcv antibody index in multiple sclerosis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209669/
https://www.ncbi.nlm.nih.gov/pubmed/30410486
http://dx.doi.org/10.3389/fimmu.2018.02435
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