| Literature DB >> 28298471 |
George R Ambalathingal1,2, Ross S Francis3,2, Mark J Smyth1,4,2, Corey Smith1, Rajiv Khanna5.
Abstract
BK polyomavirus (BKV) causes frequent infections during childhood and establishes persistent infections within renal tubular cells and the uroepithelium, with minimal clinical implications. However, reactivation of BKV in immunocompromised individuals following renal or hematopoietic stem cell transplantation may cause serious complications, including BKV-associated nephropathy (BKVAN), ureteric stenosis, or hemorrhagic cystitis. Implementation of more potent immunosuppression and increased posttransplant surveillance has resulted in a higher incidence of BKVAN. Antiviral immunity plays a crucial role in controlling BKV replication, and our increasing knowledge about host-virus interactions has led to the development of improved diagnostic tools and clinical management strategies. Currently, there are no effective antiviral agents for BKV infection, and the mainstay of managing reactivation is reduction of immunosuppression. Development of immune-based therapies to combat BKV may provide new and exciting opportunities for the successful treatment of BKV-associated complications.Entities:
Keywords: B cell responses; T cell immunity; T cells; immunotherapy; natural killer cells; pathogenesis; transplant; virus
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Year: 2017 PMID: 28298471 PMCID: PMC5355639 DOI: 10.1128/CMR.00074-16
Source DB: PubMed Journal: Clin Microbiol Rev ISSN: 0893-8512 Impact factor: 26.132