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Progressive multifocal leukoencephalopathy and other disorders caused by JC virus: clinical features and pathogenesis

Chen S. Tan, +1 more
- 01 Apr 2010 - 
- Vol. 9, Iss: 4, pp 425-437
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TLDR
The increasingly diverse populations at risk and the recent discovery of the presence of the JC virus in the grey matter invite us to reappraise the pathogenesis of thisirus in the CNS.
Abstract
Summary Progressive multifocal leukoencephalopathy (PML) is a rare but often fatal brain disease caused by reactivation of the polyomavirus JC. Knowledge of the characteristics of PML has substantially expanded since the introduction of combination antiretroviral therapy during the HIV epidemic and the development of immune reconstitution inflammatory syndrome (IRIS) in patients with PML. Recently, the monoclonal antibodies natalizumab, efalizumab, and rituximab—used for the treatment of multiple sclerosis, psoriasis, haematological malignancies, Crohn's disease, and rheumatic diseases—have been associated with PML. Additionally, the JC virus can also lead to novel neurological disorders such as JC virus granule cell neuronopathy and JC virus encephalopathy, and might also cause meningitis. The increasingly diverse populations at risk and the recent discovery of the presence of the JC virus in the grey matter invite us to reappraise the pathogenesis of this virus in the CNS.

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Crohn's disease

TL;DR: The epidemiology, immunobiology, amd natural history of Crohn's disease is discussed; new treatment goals and risk stratification of patients are described; and an evidence based rational approach to diagnosis is provided.
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Risk of natalizumab-associated progressive multifocal leukoencephalopathy.

TL;DR: Positive status with respect to anti-JC virus antibodies, prior use of immunosuppressants, and increased duration of natalizumab treatment, alone or in combination, were associated with distinct levels of PML risk in natalIZumab-treated patients with multiple sclerosis.
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Integrins as therapeutic targets: lessons and opportunities

TL;DR: The structure and function of integrins, their roles in disease and the chequered history of the approved integrin antagonists are discussed.
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Molecular biology, epidemiology, and pathogenesis of progressive multifocal leukoencephalopathy, the JC virus-induced demyelinating disease of the human brain.

TL;DR: The study of JCV and the elucidation of the underlying causes of PML are important and active areas of research that may lead to new insights into immune function and host antiviral defense, as well as to potential new therapies.

Isolation ofa Possible Archetypal JCVirusDNA Sequence from Nonimmunocompromised Individuals

TL;DR: The cloned viral DNAs all contained an archetypal regulatory sequence from which various regulatory sequences of JC polyomavirus isolates derived from patients with progressive multifocal leukoencephalopathy could have evolved by deletion and amplification.
References
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Journal ArticleDOI

Progressive Multifocal Leukoencephalopathy after Natalizumab Therapy for Crohn's Disease

TL;DR: Analysis of frozen serum samples showed that JC virus DNA had appeared in the serum three months after the initiation of open-label natalizumab monotherapy and two months before the appearance of symptomatic PML, suggesting that anti-alpha4-integrin therapy can result in JC virus-induced PML.
Journal ArticleDOI

Progressive multifocal leukoencephalopathy complicating treatment with natalizumab and interferon beta-1a for multiple sclerosis.

TL;DR: A 46-year-old woman with relapsing-remitting multiple sclerosis died from progressive multifocal leukoencephalopathy (PML) after having received 37 doses of natalizumab (300 mg every four weeks) as part of a clinical trial of nalozumab and interferon beta-1a.
Journal ArticleDOI

Progressive Multifocal Leukoencephalopathy in a Patient Treated with Natalizumab

TL;DR: The clinical course of a patient with multiple sclerosis in whom progressive multifocal leukoencephalopathy (PML) developed during treatment with interferon beta-1a and a selective adhesion-molecule blocker, natalizumab is described.
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