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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.
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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