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Mouse Kidney Transplantation: Models of Allograft Rejection
Published on: October 11, 2014
Viral infections directly involved in kidney allograft function
1Division of Nephrology and Rheumatology, Fukuoka University, Fukuoka, Japan.
Abstract:
Modern immunosuppressive therapy has dramatically reduced the incidence of acute rejection and improved graft survival in kidney transplant patients. However, infectious complications remain an important issue. Amongst the various pathogens, viruses such as adenovirus and polyomavirus BK can directly cause acute or chronic graft dysfunction. Adenovirus mainly causes haemorrhagic cystitis and tubulointerstitial nephritis in kidney transplant patients. While patients show apparent clinical symptoms such as fever, dysuria, gross haematuria, frequency and urgency of urination, and most patients show acute graft dysfunction, these symptoms and graft dysfunction are reversible. Polyomavirus BK infection, however, is asymptomatic but graft outcome is poor if the patient develops tissue-invasive nephropathy confirmed by graft biopsy. Recently, an attempt to create a pathological classification for predicting the clinical course has been made by the Banff Working Group on Polyomavirus Nephropathy. With regards to treatment, the basic strategy is a reduction of calcineurin inhibitor and/or antimetabolites, and the effectiveness of several adjunct treatments has been investigated in several clinical trials. There are other unresolved issues, such as the diagnosis of subsequent acute rejection, the definition of remission, methods of resuming immunosuppression and long-term follow-up. Most of all, development of effective vaccines and novel drug discovery are necessary to prevent the development and progression of BKV-associated nephropathy.
Insights
Kidney transplant patients face viral infections like adenovirus and polyomavirus BK, impacting graft survival. While adenovirus infections are often reversible, polyomavirus BK nephropathy poses a significant threat requiring new treatments and vaccines.
Area of Science:
- Nephrology
- Transplant Immunology
- Virology
Background:
- Immunosuppressive therapy improves kidney transplant outcomes but increases infectious complication risks.
- Viruses like adenovirus and polyomavirus BK (BKV) can cause significant kidney graft dysfunction.
Purpose of the Study:
- To review the clinical impact of viral infections, specifically adenovirus and BKV, in kidney transplant recipients.
- To discuss current diagnostic and treatment strategies for viral nephropathy post-transplant.
- To highlight unresolved issues and future directions in managing BKV-associated nephropathy.
Main Methods:
- Review of clinical manifestations and pathological findings associated with adenovirus and BKV infections.
- Analysis of current treatment approaches, including immunosuppression reduction and adjunct therapies.
- Discussion of diagnostic challenges and the need for improved classification systems (e.g., Banff Working Group).
Main Results:
- Adenovirus infections typically cause symptomatic hemorrhagic cystitis and tubulointerstitial nephritis, often reversible.
- BKV infection can lead to asymptomatic but severe nephropathy with poor graft outcomes, especially when tissue-invasive.
- Current treatment focuses on reducing immunosuppression, with ongoing trials for adjunct therapies.
Conclusions:
- Viral infections remain a critical challenge in kidney transplantation, impacting long-term graft survival.
- Effective management of BKV-associated nephropathy requires further research into diagnosis, treatment, and prevention.
- Development of vaccines and novel drugs is crucial for preventing and treating BKV nephropathy.
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