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Natalizumab-treated patients at high risk for PML persistently excrete JC polyomavirus

Sixty-three natalizumab-treated patients with relapsing multiple sclerosis were screened for JC polyomavirus (JCV) viruria. Urinary-positive patients were longitudinally sampled for up to 24 weeks. Using methods that distinguish encapsidated virus from naked viral DNA, 17.5 % of patients were found...

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Detalles Bibliográficos
Autores principales: Werner, Milton H., Huang, DeRen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5127893/
https://www.ncbi.nlm.nih.gov/pubmed/27198748
http://dx.doi.org/10.1007/s13365-016-0449-0
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author Werner, Milton H.
Huang, DeRen
author_facet Werner, Milton H.
Huang, DeRen
author_sort Werner, Milton H.
collection PubMed
description Sixty-three natalizumab-treated patients with relapsing multiple sclerosis were screened for JC polyomavirus (JCV) viruria. Urinary-positive patients were longitudinally sampled for up to 24 weeks. Using methods that distinguish encapsidated virus from naked viral DNA, 17.5 % of patients were found to excrete virus, consistent with the prevalence of urinary excretion in the general population. Unexpectedly, urinary excretion was predominantly seen (>73 %) in patients with high JC antibody index (≥2.0). Active JCV infection, therefore, tends to occur in natalizumab patients that carry a high risk factor for the development of disease, directly linking JC infection to the risk factors for PML development.
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spelling pubmed-51278932016-12-19 Natalizumab-treated patients at high risk for PML persistently excrete JC polyomavirus Werner, Milton H. Huang, DeRen J Neurovirol Short Communication Sixty-three natalizumab-treated patients with relapsing multiple sclerosis were screened for JC polyomavirus (JCV) viruria. Urinary-positive patients were longitudinally sampled for up to 24 weeks. Using methods that distinguish encapsidated virus from naked viral DNA, 17.5 % of patients were found to excrete virus, consistent with the prevalence of urinary excretion in the general population. Unexpectedly, urinary excretion was predominantly seen (>73 %) in patients with high JC antibody index (≥2.0). Active JCV infection, therefore, tends to occur in natalizumab patients that carry a high risk factor for the development of disease, directly linking JC infection to the risk factors for PML development. Springer International Publishing 2016-05-19 2016 /pmc/articles/PMC5127893/ /pubmed/27198748 http://dx.doi.org/10.1007/s13365-016-0449-0 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Short Communication
Werner, Milton H.
Huang, DeRen
Natalizumab-treated patients at high risk for PML persistently excrete JC polyomavirus
title Natalizumab-treated patients at high risk for PML persistently excrete JC polyomavirus
title_full Natalizumab-treated patients at high risk for PML persistently excrete JC polyomavirus
title_fullStr Natalizumab-treated patients at high risk for PML persistently excrete JC polyomavirus
title_full_unstemmed Natalizumab-treated patients at high risk for PML persistently excrete JC polyomavirus
title_short Natalizumab-treated patients at high risk for PML persistently excrete JC polyomavirus
title_sort natalizumab-treated patients at high risk for pml persistently excrete jc polyomavirus
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5127893/
https://www.ncbi.nlm.nih.gov/pubmed/27198748
http://dx.doi.org/10.1007/s13365-016-0449-0
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