Ambalathingal George R, Francis Ross S, Smyth Mark J, Smith Corey, Khanna Rajiv
QIMR Berghofer Centre for Immunotherapy and Vaccine Development, Tumour Immunology Laboratory, QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Faculty of Medicine, University of Queensland, Brisbane, QLD, Australia.
Clin Microbiol Rev. 2017 Apr;30(2):503-528. doi: 10.1128/CMR.00074-16.
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.
BK多瘤病毒(BKV)在儿童期常引发感染,并在肾小管细胞和尿路上皮内建立持续感染,临床影响极小。然而,肾移植或造血干细胞移植后免疫功能低下个体中BKV的重新激活可能会导致严重并发症,包括BKV相关性肾病(BKVAN)、输尿管狭窄或出血性膀胱炎。更强效免疫抑制措施的实施以及移植后监测的增加导致BKVAN的发病率升高。抗病毒免疫在控制BKV复制中起关键作用,而且我们对宿主-病毒相互作用日益深入的了解促成了改进的诊断工具和临床管理策略的发展。目前,尚无针对BKV感染的有效抗病毒药物,应对重新激活的主要方法是降低免疫抑制强度。开发基于免疫的疗法来对抗BKV可能为成功治疗BKV相关并发症带来新的令人兴奋的机遇。