Shire, A Takeda Company, Cambridge, MA, USA.
CTI Clinical Trial & Consulting Services, Covington, KY, USA.
Transpl Infect Dis. 2020 Dec;22(6):e13396. doi: 10.1111/tid.13396. Epub 2020 Jul 27.
In transplant recipients, cytomegalovirus (CMV) infection increases morbidity and mortality; furthermore, coinfection with other human herpesviruses like the Epstein-Barr virus (EBV) may complicate their management. This systematic literature review aimed to summarize rates of CMV-EBV coinfection and associated clinical outcomes among solid organ transplant (SOT) and hematopoietic stem cell transplant (HSCT) recipients.
An electronic literature search was performed using pre-specified search strategies (January 1, 2010-October 31, 2018) and following established/best practice methodology. Of 316 publications identified, 294 did not report CMV-EBV coinfection and were excluded. Studies meeting the inclusion criteria were further analyzed. Due to limited reporting/heterogeneity, data were not meta-analyzable.
Nine studies (six SOT; three HSCT) reported CMV-EBV coinfection; rates of coinfection post transplantation varied between 2.6% and 32.7%. Two studies indicated CMV reactivation to be an independent variable associated with EBV reactivation. Among SOT studies, higher rates of graft dysfunction (47.4% vs 22.9%), rejection episodes (20.0% vs 8.9%), or acute rejection (50.0% vs 31.0%) were reported for patients with coinfection than without. In HSCT studies, patients with graft-vs-host disease were not reported separately for coinfection. Two studies described cases of post-transplant lymphoproliferative disorder (PTLD) in patients with CMV-EBV coinfection and reported rates of PTLD of 92% and 100%.
The CMV-EBV coinfection rate in HSCT and SOT recipients varied and was associated with increased graft rejection and PTLD compared with patients without coinfection. Further research may improve understanding of the burden of CMV-EBV coinfection among transplant recipients.
在移植受者中,巨细胞病毒(CMV)感染会增加发病率和死亡率;此外,与其他人类疱疹病毒如 EBV 合并感染可能会使病情复杂化。本系统文献复习旨在总结实体器官移植(SOT)和造血干细胞移植(HSCT)受者中 CMV-EBV 合并感染的发生率和相关临床结局。
使用预先指定的搜索策略(2010 年 1 月 1 日至 2018 年 10 月 31 日)进行电子文献检索,并遵循既定/最佳实践方法。在 316 篇已确定的文献中,有 294 篇未报告 CMV-EBV 合并感染,被排除在外。符合纳入标准的研究进一步进行分析。由于报告有限/存在异质性,因此无法进行荟萃分析。
有 9 项研究(6 项 SOT;3 项 HSCT)报告了 CMV-EBV 合并感染;移植后合并感染的发生率在 2.6%至 32.7%之间。有两项研究表明,CMV 再激活是 EBV 再激活的独立相关变量。在 SOT 研究中,与无合并感染的患者相比,合并感染的患者更易出现移植物功能障碍(47.4% vs 22.9%)、排斥反应(20.0% vs 8.9%)或急性排斥反应(50.0% vs 31.0%)。在 HSCT 研究中,患有移植物抗宿主病的患者未单独报告合并感染的情况。有两项研究描述了合并 CMV-EBV 感染的移植后淋巴组织增生性疾病(PTLD)病例,PTLD 的发生率分别为 92%和 100%。
HSCT 和 SOT 受者中 CMV-EBV 合并感染的发生率存在差异,与无合并感染的患者相比,合并感染与移植物排斥和 PTLD 的发生率增加有关。进一步的研究可能会提高对移植受者中 CMV-EBV 合并感染负担的认识。