Northwestern University School of Medicine, Chicago, Illinois, USA.
J Heart Lung Transplant. 2009 Oct;28(10):1050-6. doi: 10.1016/j.healun.2009.04.032.
Cytomegalovirus (CMV) has been associated with morbidity, including chronic allograft rejection, in transplant recipients. Data from adult centers suggests that CMV hyperimmune globulin (CMVIG) and ganciclovir together are superior in preventing CMV viremia than ganciclovir alone.
A retrospective review of pediatric lung transplant recipients at 14 sites in North America and Europe was conducted to evaluate the effect of adding cytomegalovirus immunoglobulin (CMVIG) prophylaxis to at least 3 weeks of intravenous ganciclovir therapy in pediatric lung transplant recipients. Data were recorded for the first year after transplantation. Associations between time to CMV and risk factors, including CMVIG use, were assessed by multivariable Cox proportional hazards models.
Of 599 patients whose records were reviewed, 329 received at least 3 weeks of ganciclovir, with 62 (19%) receiving CMVIG. CMVIG was administered more frequently with CMV donor-positive/recipient-negative serostatus (p < 0.05). In multivariable models, patients who did not receive CMVIG as part of their prophylaxis were 3 times more likely to develop CMV infection (hazard ratio, 3.4; 95% confidence interval, 1.2-9.5) independent of CMV serostatus. However, CMVIG administration was not associated with decreased risk of episodes of CMV disease. Receipt of CMVIG was not associated with decreased risks of post-transplant morbidities (acute rejection, respiratory viral infection or early bronchiolitis obliterans) or morbidity within the first year after pediatric lung transplantation.
The use of CMVIG in addition to antiviral prophylaxis in pediatric lung transplantation requires further evaluation.
巨细胞病毒(CMV)与发病率有关,包括移植受者的慢性同种异体移植排斥反应。成人中心的数据表明,CMV 免疫球蛋白(CMVIG)和更昔洛韦联合使用在预防 CMV 病毒血症方面优于更昔洛韦单独使用。
对北美和欧洲 14 个地点的儿科肺移植受者进行了回顾性研究,以评估在儿科肺移植受者中,至少 3 周静脉用更昔洛韦治疗的基础上加用 CMV 免疫球蛋白(CMVIG)预防 CMV 病毒血症的效果。记录移植后第一年的数据。通过多变量 Cox 比例风险模型评估 CMV 时间与危险因素(包括 CMVIG 使用)之间的关联。
在回顾的 599 例患者记录中,329 例接受了至少 3 周的更昔洛韦治疗,其中 62 例(19%)接受了 CMVIG。CMVIG 的使用与 CMV 供体阳性/受体阴性血清学状态更频繁相关(p<0.05)。在多变量模型中,未接受 CMVIG 作为预防措施一部分的患者发生 CMV 感染的可能性是未接受 CMVIG 患者的 3 倍(风险比,3.4;95%置信区间,1.2-9.5),与 CMV 血清学状态无关。然而,CMVIG 的使用与 CMV 疾病发作的风险降低无关。接受 CMVIG 与移植后发病率(急性排斥反应、呼吸道病毒感染或早期细支气管炎闭塞)或儿科肺移植后第一年的发病率降低无关。
CMVIG 在儿科肺移植中联合抗病毒预防的使用需要进一步评估。