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Measurement of BK-polyomavirus Non-Coding Control Region Driven Transcriptional Activity Via Flow Cytometry
Published on: July 13, 2019
Cytomegalovirus and polyomavirus BK posttransplant
Adrian Egli1, Simone Binggeli, Sohrab Bodaghi
1Transplantation Virology, Institute for Medical Microbiology, Department of Clinical & Biological Sciences, Petersplatz 10, CH-4003 Basel, Switzerland.
Cytomegalovirus (CMV) and BK virus (BKV) are significant post-transplant threats, impacting patient and graft survival. This review covers diagnostic and therapeutic strategies for managing these viral infections in transplant recipients.
Area of Science:
- Immunology
- Virology
- Transplantation Medicine
Background:
- Post-transplant viral infections, particularly cytomegalovirus (CMV) and BK virus (BKV), pose significant risks to patient and graft survival.
- Increased immunosuppression, while reducing graft rejection, enhances susceptibility to viral pathogens like CMV and BKV.
- CMV and BKV infections can lead to severe complications, affecting multiple organ systems and reducing long-term transplant outcomes.
Purpose of the Study:
- To review the diagnostic and therapeutic strategies for managing cytomegalovirus (CMV) and BK virus (BKV) infections in transplant patients.
- To highlight the challenges posed by CMV and BKV, including their impact on graft survival and the emergence of antiviral resistance.
- To discuss the current approaches to controlling these viral infections, emphasizing the role of immune modulation for BKV.
Main Methods:
- Literature review of diagnostic and therapeutic interventions for CMV and BKV post-transplantation.
- Analysis of the impact of immunosuppression on viral replication and disease progression.
- Examination of current treatment strategies, including antiviral therapies and immune-based approaches.
Main Results:
- Cytomegalovirus (CMV) remains a major viral pathogen post-transplant, causing widespread organ involvement and resistance to antivirals.
- BK virus (BKV) primarily affects the reno-urinary tract, leading to nephropathy and hemorrhagic cystitis, with treatment relying on immune reconstitution.
- Both CMV and BKV significantly reduce graft and patient survival, necessitating effective management strategies.
Conclusions:
- Effective management of CMV and BKV is crucial for improving outcomes in solid organ and hematopoietic stem cell transplant recipients.
- The development of novel diagnostic and therapeutic approaches is essential to combat viral infections and enhance long-term graft and patient survival.
- Balancing immunosuppression to control viral replication while preventing graft rejection remains a critical challenge in transplantation.
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