Emerging viral diseases in kidney transplant recipients

被引:9
|
作者
Moal, Valerie [1 ,2 ]
Zandotti, Christine [3 ]
Colson, Philippe [2 ,3 ]
机构
[1] CHU Concept, APHM, Ctr Nephrol & Transplantat Renale, F-13385 Marseille 05, France
[2] Aix Marseille Univ, Inserm 1095, IRD 198, URMITE,CNRS 7278,UM63, Marseille, France
[3] CHU Timone, APHM, Marseille, France
关键词
WEST-NILE-VIRUS; PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY; HEPATITIS-E VIRUS; PARVOVIRUS B19 INFECTION; PRIMARY EFFUSION LYMPHOMA; RENAL-TRANSPLANTATION; BK VIRUS; KAPOSIS-SARCOMA; CASTLEMANS-DISEASE; LYMPHOPROLIFERATIVE DISORDER;
D O I
10.1002/rmv.1732
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Viruses are the most important cause of infections and a major source of mortality in Kidney Transplant Recipients (KTRs). These patients may acquire viral infections through exogenous routes including community exposure, donor organs, and blood products or by endogenous reactivation of latent viruses. Beside major opportunistic infections due to CMV and EBV and viral hepatitis B and C, several viral diseases have recently emerged in KTRs. New medical practices or technologies, implementation of new diagnostic tools, and improved medical information have contributed to the emergence of these viral diseases in this special population. The purpose of this review is to summarize the current knowledge on emerging viral diseases and newly discovered viruses in KTRs over the last two decades. We identified viruses in the field of KT that had shown the greatest increase in numbers of citations in the NCBI PubMed database. BKV was the most cited in the literature and linked to an emerging disease that represents a great clinical concern in KTRs. HHV-8, PVB19, WNV, JCV, H1N1 influenza virus A, HEV, and GB virus were the main other emerging viruses. Excluding HHV8, newly discovered viruses have been infrequently linked to clinical diseases in KTRs. Nonetheless, pathogenicity can emerge long after the discovery of the causative agent, as has been the case for BKV. Overall, antiviral treatments are very limited, and reducing immunosuppressive therapy remains the cornerstone of management. Copyright (C) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:50 / 69
页数:20
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