肾移植后病毒感染:CMV和BK

Večerić-Haler Željka, Kojc Nika
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引用次数: 2

摘要

机会性感染通常发生在肾移植后的前6个月,包括巨细胞病毒(CMV)和多瘤病毒。病毒性病原体,如巨细胞病毒和多瘤病毒、JC或BK病毒(BKV),能够在肾脏中复制和/或引起全身性疾病,在免疫功能低下的宿主中,这些病原体的症状性感染可能与显著的发病率和死亡率相关。虽然BK病毒通常在肾移植中复制,引起BK病毒肾病(BKN),并伴有尿中的特征性诱饵细胞,但巨细胞病毒感染更常导致涉及胃肠道(GIT)、肺或肝脏的全身性感染,仅在肾移植中偶有发现。在这两种情况下,疾病通常是由于潜伏病毒的再激活。因此,预防和早期治疗移植后感染对肾移植受者至关重要。由于BKV病毒血症和病毒血症可以在没有肾损伤和病毒性肾病的情况下看到,因此BKV的诊断必须通过肾活检来证实。迄今为止,预防性治疗是巨细胞病毒感染的最佳策略,而对于BKV感染,除了减少免疫抑制外,没有可用的标准治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Viral Infections after Kidney Transplantation: CMV and BK
Opportunistic infections commonly occur during the first 6 months after kidney transplant, including cytomegalovirus (CMV) and polyomaviruses. Viral pathogens such as CMV and polyomaviruses, JC or BK virus (BKV), are able to replicate in the kidney and/or cause systemic disease, and symptomatic infection with these agents can be associated with significant morbidity and mortality in immunocompromised host. While BK virus usually replicates in kidney transplant causing BK virus nephropathy (BKN) with characteristic decoy cells in the urine, CMV infection more often leads to systemic infection involving the gastrointestinal tract (GIT), lungs, or liver and can only sporadically be detected in renal transplant. In both cases, the disease is most often due to reactivation of a latent virus. Prevention and early treatment of posttransplant infection are therefore crucial with kidney transplant recipients. Since BKV viruria and viremia can be seen without renal injury and viral nephropathy, a diagnosis of BKN must be confirmed by renal biopsy. To date, preemptive treatment is the best strategy for CMV infection, while no available standard therapy, except for reduction of immunosuppression, is available for BKV infection.
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