Wiseman Alexander C
Division of Renal Diseases and Hypertension, University of Colorado Health Sciences Center, Aurora, CO 80045, USA.
Am J Kidney Dis. 2009 Jul;54(1):131-42. doi: 10.1053/j.ajkd.2009.01.271. Epub 2009 Apr 25.
During the last decade, the human polyomaviruses (BK virus and, much less commonly, JC virus) have entered the realm of routine clinical decision making for providers caring for kidney transplant recipients. The emergence of polyomavirus-associated nephropathy (PVAN) as an important clinical entity coincided with the development and use of more potent immunosuppression agents, currently the only clear risk factor for reactivation of the virus. Ongoing efforts to define the pathogenesis, clinical presentation, and appropriate management of PVAN have led to a greater ability to prevent and control viral-induced interstitial nephritis despite continued deficiencies in our understanding of risk factors for disease and lack of published prospective polyomavirus-specific antiviral trials. The purpose of this review is to summarize advances made during the last decade and highlight emerging data that address common clinical considerations the clinician currently faces in the understanding and management of PVAN.
在过去十年中,人多瘤病毒(BK病毒,以及更罕见的JC病毒)已进入为肾移植受者提供护理的医疗人员日常临床决策的范畴。多瘤病毒相关性肾病(PVAN)作为一种重要的临床实体的出现,与更有效的免疫抑制剂的开发和使用同时发生,目前这是该病毒再激活的唯一明确风险因素。尽管我们对疾病风险因素的理解仍存在不足,且缺乏已发表的前瞻性多瘤病毒特异性抗病毒试验,但目前在确定PVAN的发病机制、临床表现和适当管理方面所做的努力,已使我们在预防和控制病毒诱导的间质性肾炎方面有了更强的能力。本综述的目的是总结过去十年取得的进展,并强调新出现的数据,这些数据涉及临床医生目前在理解和管理PVAN时面临的常见临床考量。