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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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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. |
format | Online Article Text |
id | pubmed-5127893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
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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