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Published on: July 13, 2019
Routine immunohistochemistry study for polyomavirus BK nephropathy in transplanted kidney biopsies, is it
Fatemeh Nili1, Maliheh Mohammadhoseini2, Seyed Mohammadreza Khatami3
1Department of Pathology, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, I.R. of Iran. f-nili@sina.tums.ac.ir.
Early diagnosis of Polyomavirus BK Nephropathy (PVBKN) in kidney transplant patients is improved with immunohistochemistry (IHC). Routine IHC for SV40 antigen increases diagnostic sensitivity for detecting this challenging condition.
Area of Science:
- Nephrology
- Transplantation Immunology
- Virology
Background:
- Polyomavirus BK Nephropathy (PVBKN) poses diagnostic challenges in kidney transplant recipients.
- Current gold standard histopathology may miss early-stage PVBKN, as viral inclusions are not always apparent.
- Immunohistochemistry (IHC) is a potential diagnostic tool, but its routine use lacks consensus.
Purpose of the Study:
- To evaluate the diagnostic utility of immunohistochemistry (IHC) for Simian Virus 40 (SV40) antigen in identifying early Polyomavirus BK Nephropathy (PVBKN).
- To compare the sensitivity and specificity of histopathology with and without IHC in diagnosing PVBKN in transplanted kidneys.
Main Methods:
- Retrospective analysis of 275 transplanted kidney biopsy samples from 2016-2019.
- Samples were evaluated using routine stains and IHC for SV40 antigen.
- PVBKN diagnosis was confirmed by typical viral inclusions or positive IHC staining (≥1+).
Main Results:
- 18 cases (6.5%) of PVBKN were diagnosed.
- Histopathology alone detected typical viral inclusions in 77.7% of PVBKN cases.
- IHC identified an additional 22.2% of PVBKN cases missed by routine histopathology, demonstrating higher sensitivity.
Conclusions:
- Routine IHC for SV40 antigen significantly enhances diagnostic sensitivity for early-stage PVBKN in kidney transplant biopsies.
- Implementing routine IHC can improve the early detection and management of PVBKN.
- This approach aids in timely intervention for patients with new-onset allograft dysfunction.
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