Plasma levels of JC virus are sensitive and specific for detecting and predicting progressive multifocal leukoencephalopathy in HIV patients

Author:

Bayliss Julianne1,Cherry Catherine L234,McLean Catriona A25

Affiliation:

1. Division of Molecular Research & Development, Victorian Infectious Diseases Reference Laboratory, North Melbourne, VIC 3051, Australia.

2. Department of Medicine, Monash University, Alfred Hospital, Melbourne, VIC 3004, Australia

3. Centre for Virology, Burnet Institute, Melbourne, VIC 3004, Australia

4. Infectious Diseases Unit, Alfred Hospital, Melbourne, VIC 3004, Australia

5. Anatomical Pathology, Alfred Hospital, Melbourne, VIC 3004, Australia

Abstract

Aims: HIV-1 infection represents the most common immunosuppressive condition associated with progressive multifocal leukoencephalopathy (PML). Materials & methods: Nested PCR and quantitative real-time PCR (qPCR) for JC virus (JCV) DNA was performed on serial plasma samples obtained from 14 HIV patients with PML and 27 matched controls. Results: JCV large T antigen (LT) DNA was detected via qPCR in 11 out of 14 (79%) PML patients at disease onset and four out of 27 (15%) controls (p < 0.001). JCV LT qPCR was associated with PML diagnosis, duration of known HIV infection, absence of a prior AIDS-defining illness and absence of combination antiretroviral therapy (p < 0.001; R2 = 0.35). JCV LT qPCR was more likely to be positive in the 8 months prior to PML diagnosis compared with earlier samples (p = 0.01). Conclusion: Detection of JCV DNA in plasma of HIV infected patients via qPCR may represent a valuable test for identifying patients at risk of developing PML.

Publisher

Future Medicine Ltd

Subject

Virology

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