Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/26419
Title: High rates of JCV seroconversion in a large international cohort of natalizumab-treated patients.
Austin Authors: Dwyer, Christopher M;Jokubaitis, Vilija G;Stankovich, Jim;Baker, Josephine;Haartsen, Jodi;Butzkueven, Helmut;Cartwright, Adriana;Shuey, Neil;Fragoso, Yara Dadalti;Rath, Louise;Skibina, Olga;Fryer, Kylie;Butler, Ernest;Coleman, Jennifer;MacIntrye, Jennifer;Macdonell, Richard A L ;van der Walt, Anneke
Affiliation: Universidade Metropolitana de Santos, São Paulo, Brazil
Department of Neurology, Monash Health, Clayton, VC, Australia
Eastern Clinical Research Unit, Department of Neurology, Box Hill Hospital, Melbourne, VIC, Australia
Melbourne Brain Centre, Royal Melbourne Hospital, Parkville, VC, Australia
Department of Neuroscience, Monash University, Melbourne, VC, Australia
Melbourne Brain Centre, Royal Melbourne Hospital, 300 Grattan Street, Parkville, VC 3050, Australia
Department of Neuroscience, Monash University, 99 Commercial Rd, Melbourne, VC 3004, Australia
Neurology
Department of Neurology, The Alfred Hospital, Melbourne, VC, Australia
Department of Neurology, St Vincent's Hospital, Melbourne, VIC, Australia
Issue Date: 16-Apr-2021
Date: 2021
Publication information: Therapeutic Advances in Neurological Disorders 2021; 14: 1756286421998915
Abstract: To retrospectively assess factors associated with John Cunningham virus (JCV) seroconversion in natalizumab-treated patients. Natalizumab is highly effective for the treatment of relapsing-remitting multiple sclerosis (RRMS), but its use is complicated by opportunistic JCV infection. This virus can result in progressive multifocal leukoencephalopathy (PML). Serial assessment of JCV serostatus is mandated during natalizumab treatment. Patients treated with natalizumab for RRMS at six tertiary hospitals in Melbourne, Australia (n = 865) and 11 MS treatment centres in Brazil (n = 136) were assessed for change in JCV serostatus, duration of exposure to natalizumab and prior immunosuppression. Sensitivity analyses examined whether sex, age, tertiary centre, prior immunosuppression or number of JCV tests affected time to seroconversion. From a cohort of 1001 natalizumab-treated patients, durable positive seroconversion was observed in 83 of 345 initially JCV negative patients (24.1%; 7.3% per year). Conversely, 16 of 165 initially JCV positive patients experienced durable negative seroconversion (9.7%; 3.8% per year). Forty patients (3.9%) had fluctuating serostatus. Time-to-event analysis did not identify a relationship between JCV seroconversion and duration of natalizumab exposure. Prior exposure to immunosuppression was not associated with an increased hazard of positive JCV seroconversion. Male sex was associated with increased JCV seroconversion risk [adjusted hazard ratio 2.09 (95% confidence interval 1.17-3.71) p = 0.012]. In this large international cohort of natalizumab-treated patients we observed an annual durable positive seroconversion rate of 7.3%. This rate exceeds that noted in registration and post-marketing studies for natalizumab. This rate also greatly exceeds that predicted by epidemiological studies of JCV seroconversion in healthy populations. Taken together, our findings support emerging evidence that natalizumab causes off-target immune changes that may be trophic for JCV seroconversion. In addition, male sex may be associated with increased positive JCV seroconversion.
URI: https://ahro.austin.org.au/austinjspui/handle/1/26419
DOI: 10.1177/1756286421998915
ORCID: 0000-0001-6387-6585
0000-0002-4278-7003
Journal: Therapeutic Advances in Neurological Disorders
PubMed URL: 33948117
ISSN: 1756-2856
Type: Journal Article
Subjects: John Cunningham virus
Multiple sclerosis
natalizumab
seroconversion
Appears in Collections:Journal articles

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