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JC Polyomavirus Infection: A Narrative Review
Meital Elbaz1,2, Dafna Yahav3,4, Yair Mina3,5
1Infectious Diseases Unit, Sourasky Medical Center, Tel Aviv, Israel. meitalzuz@gmail.com.
Abstract:
Progressive multifocal leukoencephalopathy (PML) is a devastating and often fatal central nervous system infection caused by John Cunningham polyomavirus virus (JCPyV). PML results from JCPyV reactivation in the setting of impaired cellular immunity in patients with HIV, organ transplantation, severe inflammatory disease, and an increasing number of modern treatments for cancer and autoimmune diseases. The presence of clinical and imaging manifestations consistent with the diagnosis coupled with the demonstration of JCPyV by PCR in cerebrospinal fluid (CSF) are considered diagnostic. Since there are no effective antiviral treatments available, restoring immune function is a key component in PML treatment. Novel immunotherapeutic approaches can ameliorate PML. Immunotherapeutic interventions, such as use of checkpoint inhibitors and viral specific T-cell, have shown promising results, but additional data are needed. In this review, we summarize the available data on risk factors for JCPyV neurological syndrome, clinical, laboratory, and radiological features, and propose an algorithm for management.
Insights
Progressive multifocal leukoencephalopathy (PML) is a severe JCPyV infection impacting the central nervous system. Restoring immune function is key, with novel immunotherapies showing promise for PML treatment.
Area of Science:
- Neurovirology
- Immunology
- Infectious Diseases
Background:
- Progressive multifocal leukoencephalopathy (PML) is a rare, fatal central nervous system infection caused by John Cunningham polyomavirus (JCPyV).
- PML occurs due to JCPyV reactivation in immunocompromised individuals, including those with HIV, organ transplants, autoimmune diseases, and certain cancer treatments.
- Diagnosis relies on clinical presentation, imaging, and JCPyV detection in cerebrospinal fluid (CSF) via PCR.
Purpose of the Study:
- To review risk factors, clinical, laboratory, and radiological features of JCPyV-associated PML.
- To propose a management algorithm for PML.
- To highlight emerging immunotherapeutic strategies for PML.
Main Methods:
- Literature review of JCPyV and PML.
- Analysis of diagnostic criteria for PML.
- Evaluation of current and novel treatment approaches, including immunotherapies.
Main Results:
- JCPyV reactivation is linked to impaired cellular immunity across various conditions.
- Diagnosis is established through a combination of clinical, imaging, and laboratory findings (CSF PCR for JCPyV).
- Current treatment focuses on immune restoration, as no effective antiviral therapies exist.
Conclusions:
- PML is a serious JCPyV infection requiring prompt diagnosis and management.
- Restoring immune function is the cornerstone of PML treatment.
- Novel immunotherapies, like checkpoint inhibitors and T-cell therapies, offer potential but require further investigation.
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