Abstract
After pediatric kidney transplantation BK polyomavirus (BKPyV) infections are associated with an increased risk of graft loss by BKPyV-associated nephropathy (BkPyVAN). However, suitable prognostic markers for the individual outcome of BKPyV infections are missing and the management of therapeutic interventions remains a challenge to the success of pediatric kidney transplantation. This review gives an overview on current diagnostic and therapeutic strategies in the field of BKPyV infections after pediatric kidney transplantation. Methods determining the individual immune response to BKPyV are described and their usability is discussed. There is growing evidence that BKPyV-specific T cells (BKPyV-Tvis) may serve as prognostic markers in order to steer immunosuppressive therapy in pediatric kidney recipients with BKPyV viremia in future. Prospective randomized trials in viremic kidney recipients comparing Tvis-steered therapeutic intervention with standard reduction of immunosuppression are needed before implementation of BKPyV-Tvis monitoring in routine care of BKPyV infections.
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Abbreviations
- BKPyV:
-
BK polyomavirus
- BKPyVAN:
-
BK polyomavirus-associated nephropathy
- CMV:
-
Cytomegalovirus
- CsA:
-
Cyclosporine A
- EBV:
-
Epstein Barr virus
- ELISpot:
-
Enzyme-linked immunospot
- IVIG:
-
Intravenous immunoglobulin
- mTOR:
-
Mammalian target of rapamycin
- PCR:
-
Polymerase chain reaction
- TAC:
-
Tacrolimus
- Tvis:
-
Virus-specific T cells
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Acknowledgements
We thank Jan Hinrich Bräsen, Department of Pathology, Hanover Medical School, for providing Figure 1.
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Ahlenstiel-Grunow, T., Pape, L. Diagnostics, treatment, and immune response in BK polyomavirus infection after pediatric kidney transplantation. Pediatr Nephrol 35, 375–382 (2020). https://doi.org/10.1007/s00467-018-4164-3
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DOI: https://doi.org/10.1007/s00467-018-4164-3