| Literature DB >> 33809472 |
Chia-Lin Shen1,2,3, Bo-Sheng Wu3,4, Tse-Jen Lien1,3,5, An-Hang Yang3,4,6, Chih-Yu Yang1,3,4,7,8.
Abstract
BK polyomavirus nephropathy (BKVN) and allograft rejection are two closely-associated diseases on opposite ends of the immune scale in kidney transplant recipients. The principle of balancing the immune system remains the mainstay of therapeutic strategy. While patient outcomes can be improved through screening, risk factors identification, and rapid reduction of immunosuppressants, a lack of standard curative therapy is the primary concern during clinical practice. Additionally, difficulty in pathological differential diagnosis and clinicopathology's dissociation pose problems for a definite diagnosis. This article discusses the delicate evaluation needed to optimize immunosuppression and reviews recent advances in molecular diagnosis and immunological therapy for BKVN patients. New biomarkers for BKVN diagnosis are under development. For example, measurement of virus-specific T cell level may play a role in steering immunosuppressants. The development of cellular therapy may provide prevention, even a cure, for BKVN, a complex post-transplant complication.Entities:
Keywords: BK polyomavirus nephropathy; acute rejection; immunosuppressants; kidney transplant; tacrolimus
Year: 2021 PMID: 33809472 PMCID: PMC7998398 DOI: 10.3390/v13030487
Source DB: PubMed Journal: Viruses ISSN: 1999-4915 Impact factor: 5.048