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Measurement of BK-polyomavirus Non-Coding Control Region Driven Transcriptional Activity Via Flow Cytometry
Published on: July 13, 2019
BK polyoma virus nephropathy in the native kidney
Shree G Sharma1, Volker Nickeleit, Leal C Herlitz
1Department of Pathology, ColumbiaUniversity Medical Center, New York, NY, USA. drshreegopal@gmail.com
Background:
While BK polyoma virus nephropathy (PVN) is a well-recognized cause of renal allograft dysfunction, PVN of native kidneys is likely under-recognized.
Methods:
We present the pathologic features, risk factors and outcomes of eight cases of PVN in native kidneys.
Results:
The cohort included eight males aged 16-73 years (mean 47.4) with an immunocompromised state (mean duration 3.15 years) attributable to: hematologic malignancies (n = 6), for which three had undergone bone marrow transplant; lung transplant (n = 1) and combined tuberculosis and diabetes (n = 1). Seven patients were receiving specific immunosuppressive therapies. Patients were biopsied for acute kidney injury (AKI) with rise in mean creatinine levels from baseline 1.6 to 2.8 mg/dL. Pathology showed BK PVN with characteristic intranuclear inclusions staining positive for SV40 T antigen and negative for JC virus (JCV), with positive serum and/or urine PCR for BK virus. One patient had focal medullary JCV co-infection. Two patients also had renal infiltration by chronic lymphocytic leukemia (CLL). Six patients received specific therapy directed to PVN (cidofovir or leflunomide). Follow-up ranged from 2 to 20 (mean 10) months. Despite marked decrease in serum BK viral copy numbers, creatinine continued to rise in six cases (mean 3.7 mg/dL in four, requiring dialysis in two) and three patients died of malignancy, opportunistic infection or renal failure. Advanced histologic stage of PVN, ineffective antiviral therapy, co-morbidities and persistent immunocompromised state likely contributed to the poor outcomes.
Conclusion:
A high level of suspicion in immunocompromised patients is needed to diagnose PVN in an early stage that may respond more favorably to antiviral therapy.
Insights
Polyoma virus nephropathy (PVN) in native kidneys is under-recognized in immunocompromised patients. Early diagnosis and treatment are crucial for better outcomes in BK polyoma virus infections.
Area of Science:
- Nephrology
- Virology
- Immunology
Background:
- BK polyoma virus nephropathy (PVN) is a known cause of kidney transplant dysfunction.
- PVN in native kidneys is often under-recognized, despite its potential for severe renal damage.
Purpose of the Study:
- To describe the pathological features, risk factors, and outcomes of PVN in native kidneys.
- To highlight the importance of early diagnosis in immunocompromised individuals.
Main Methods:
- Retrospective analysis of eight native kidney PVN cases.
- Review of patient demographics, clinical presentation, immunosuppression status, pathology, viral markers, and treatment.
- Assessment of outcomes including renal function and survival.
Main Results:
- Eight immunocompromised males (age 16-73) with hematologic malignancies, transplants, or other conditions presented with acute kidney injury.
- Pathology confirmed BK PVN with positive SV40 T antigen staining; some cases had JCV co-infection or CLL infiltration.
- Despite treatment, six patients experienced worsening renal function, and three died, indicating poor outcomes linked to advanced disease and persistent immunosuppression.
Conclusions:
- A high index of suspicion for PVN is essential in immunocompromised patients presenting with acute kidney injury.
- Early diagnosis and prompt antiviral therapy may improve outcomes for native kidney PVN.
- Persistent immunosuppression and advanced disease stage are associated with unfavorable prognoses.
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