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Dynamic expression of JC virus in urine and its relationship to serostatus.

Authors :
Berger JR
Danaher RJ
Dobbins J
Do D
Miller CS
Source :
Multiple sclerosis and related disorders [Mult Scler Relat Disord] 2020 Jun; Vol. 41, pp. 101972. Date of Electronic Publication: 2020 Feb 04.
Publication Year :
2020

Abstract

Background: There is limited information regarding the daily shedding of JC virus (JCV) in urine and its correlation with serum JCV antibody levels.<br />Methods: The dynamic expression of JCV in urine and its correlation with JCV antibody status in patients receiving disease modifying therapy for multiple sclerosis were examined in a longitudinal case-control study. JCV antibody index levels were determined using a two-step ELISA (Stratify). JCV shedding in urine samples was determined by quantitative PCR during two 30-day study periods separated by intervals of at least 6 months.<br />Results: Of 42 study subjects (57% female; ages 22-56, average age 39.6 years), 27 (64.3%) were JCV antibody positive (index >0.40) at initial urine collection. Twelve seropositive subjects (44.4%) had detectable JCV in their urine with values ranging from 290 to 5.08 × 10 <superscript>8</superscript> copies/mL. Daily viral shedding in these patients remained fairly constant throughout the study. Urinary JCV shedding was not detected in any JCV antibody index negative or indeterminate subject. In JCV urinary shedders, the average JCV antibody index was 2.69 (range 1.67-3.57). The average anti-JCV antibody index for the remaining JCV seropositive individuals without viral urinary shedding was 1.35 (range 0.46-3.91).<br />Conclusion: MS patients displayed a consistent pattern of JCV shedding over days and months in which higher levels of viruria appeared to have driven higher levels of JCV antibody index. The findings provide additional insights into the dynamic expression of JCV and host response; however, studies in larger populations and of longer duration will be needed to determine their significance to the development of progressive multifocal leukoencephalopathy (PML).<br />Competing Interests: Declaration of Competing Interest Dr. Joseph R. Berger has been a consultant for Amgen, Biogen, Celgene, Genentech/Roche, Merck/Serono, Millennium/Takeda, Novartis, and Shire during the course of the study. He serves on the scientific advisory boards of Excision-Bio and Inhibikase and has received a grant from Biogen for the conduct of this study. Dr. Robert J. Danaher has nothing to disclose. Jessica Dobbins has nothing to disclose. Dr. David Do has nothing to disclose. Dr. Craig S. Miller has nothing to disclose.<br /> (Copyright © 2020 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
2211-0356
Volume :
41
Database :
MEDLINE
Journal :
Multiple sclerosis and related disorders
Publication Type :
Academic Journal
Accession number :
32135498
Full Text :
https://doi.org/10.1016/j.msard.2020.101972