Department of Infectious Diseases, Peter MacCallum Cancer Centre.
The Peter Doherty Institute for Infection and Immunity, The University of Melbourne and Royal Melbourne Hospital.
Curr Opin Infect Dis. 2018 Dec;31(6):481-489. doi: 10.1097/QCO.0000000000000502.
Invasive fungal disease (IFD) and cytomegalovirus (CMV) infections occur frequently, either concomitantly or sequentially in immune-compromised hosts. Although there is extensive knowledge of the risk factors for these infections as single entities, the inter-relationship between opportunistic fungii and CMV has not been comprehensively explored.
Both solid organ and stem cell transplant recipients who develop CMV invasive organ disease are at an increased risk of developing IFD, particularly aspergillosis and Pneumocystis pneumonia (PCP). Moreover, CMV viremia and recipient CMV serostatus also increased the risk of both early and late-onset IFD. Treatment-related factors, such as ganciclovir-induced neutropenia and host genetic Toll-like receptor (TLR) polymorphisms are likely to be contributory. Less is known about the relationship between CMV and IFD outside transplantation, such as in patients with hematological cancers or other chronic immunosuppressive conditions. Finally, few studies report on the relationship between CMV-specific treatments or the viral/antigen kinetics and its influence on IFD management.
CMV infection is associated with increased risk of IFD in posttransplant recipients because of a number of overlapping and virus-specific risk factors. Better understanding of how CMV virus, its related treatment, CMV-induced immunosuppression and host genetic factors impact on IFD is warranted.
侵袭性真菌病(IFD)和巨细胞病毒(CMV)感染在免疫功能低下的宿主中经常同时或先后发生。尽管人们对这些感染的单一危险因素有广泛的了解,但机会性真菌和 CMV 之间的相互关系尚未得到全面探讨。
发生 CMV 侵袭性器官疾病的实体器官和干细胞移植受者发生 IFD 的风险增加,尤其是曲霉菌病和卡氏肺孢子虫肺炎(PCP)。此外,CMV 病毒血症和受者 CMV 血清状态也增加了早发和迟发性 IFD 的风险。治疗相关因素,如更昔洛韦诱导的中性粒细胞减少症和宿主遗传 Toll 样受体(TLR)多态性可能是促成因素。CMV 与 IFD 之间的关系在移植以外的情况下(如血液系统癌症或其他慢性免疫抑制性疾病患者)知之甚少。最后,很少有研究报告 CMV 特异性治疗或病毒/抗原动力学及其对 IFD 管理的影响之间的关系。
CMV 感染与移植后受者 IFD 风险增加有关,因为存在许多重叠和病毒特异性危险因素。需要更好地了解 CMV 病毒、相关治疗、CMV 诱导的免疫抑制和宿主遗传因素如何影响 IFD。