Microbiology Service, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.
Hematology Department, Hospital Clínico Universitario, INCLIVA Research Institute, Valencia, Spain.
Transpl Infect Dis. 2021 Aug;23(4):e13627. doi: 10.1111/tid.13627. Epub 2021 May 18.
The potential role of active CMV infection in promoting acute Graft-versus-Host Disease (aGvHD) in allogeneic hematopoietic stem cell transplantation (allo-HSCT) remains a matter of debate. We further addressed this issue conducting a retrospective, observational, multicenter study of 632 patients subjected to allogeneic peripheral blood HSCT at 20 Spanish centers. Monitoring of CMV DNA load in plasma or whole blood was performed by real-time PCR assays. Cumulative incidence of CMV DNAemia was 48.9% (95% CI, 45%-52.9%), of any grade aGvHD, 45.6; 95% (CI, 41.3%-50.1%), and of grade II-IV aGvHD, 30.7 (95% CI, 24.9%-36.4%). Overall, development of CMV DNAemia at any level resulted in an increased risk of subsequent all grade (HR, 1.38; 95% CI, 1.08 - 1.76; P = .009) or grade II-IV (HR, 1.58; 95% CI, 1.22 - 2.06; P = .001) aGvHD. The increased risk of aGvHD linked to prior occurrence of CMV DNAemia was similar to the above when only clinically significant episodes were considered for the analyses (HR for all grade aGvHD, 1.48; 95% CI, 1.13 - 1.91; P = .041, and HR for grade II-IV aGvHD, 1.53; 95% CI. 1.13-1.81; P = .04). The CMV DNA doubling time in blood was comparable overall in episodes of CMV DNAemia whether followed by aGvHD or not. Whether CMV replication is a surrogate risk marker of aGvHD or it is causally involved is an important question to be addressed in future experimental research.
巨细胞病毒(CMV)感染在异基因造血干细胞移植(allo-HSCT)中促进急性移植物抗宿主病(aGvHD)的潜在作用仍然存在争议。我们通过在西班牙 20 个中心进行的一项回顾性、观察性、多中心研究进一步解决了这个问题,该研究纳入了 632 例接受异基因外周血 HSCT 的患者。通过实时 PCR 检测监测血浆或全血中的 CMV DNA 载量。CMV DNA 血症的累积发生率为 48.9%(95%CI,45%-52.9%),任何级别 aGvHD 的发生率为 45.6%(95%CI,41.3%-50.1%),2-4 级 aGvHD 的发生率为 30.7%(95%CI,24.9%-36.4%)。总体而言,任何水平的 CMV DNA 血症的发生都会增加随后发生任何级别(HR,1.38;95%CI,1.08-1.76;P=0.009)或 2-4 级(HR,1.58;95%CI,1.22-2.06;P=0.001)aGvHD 的风险。当仅考虑分析中具有临床意义的发作时,与 CMV DNA 血症相关的 aGvHD 风险增加与上述情况相似(所有级别 aGvHD 的 HR,1.48;95%CI,1.13-1.91;P=0.041,2-4 级 aGvHD 的 HR,1.53;95%CI,1.13-1.81;P=0.04)。无论是否发生 aGvHD,CMV DNA 倍增时间在血液中的 CMV DNA 血症发作中总体上是相似的。CMV 复制是否是 aGvHD 的替代风险标志物,或者是否是因果关系,这是未来实验研究中需要解决的一个重要问题。