Division of Nephrology, Department of Pediatrics, Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Child Health Evaluative Sciences, Research Institute, The Hospital for Sick Children, Toronto, ON, Canada.
Transplantation. 2018 Aug;102(8):1391-1396. doi: 10.1097/TP.0000000000002115.
Late cytomegalovirus (CMV) infection can occur after cessation of viral prophylaxis in kidney transplant recipients, yet, timing of infection is unclear and longer duration of prophylaxis may be warranted.
We conducted a retrospective cohort study of 86 children (35 CMV donor seropositive, recipient seronegative [D + R-] and 51 CMV recipient seropositive [R+]) younger than 18 years who received a kidney transplant between January 2002 and June 2014 and were treated with antiviral prophylaxis for 3 months after transplantation. Incidence of CMV DNAemia and CMV disease was determined using Kaplan-Meier analyses and risk factors were assessed using Poisson regression.
Of the 86 children, 61.6% were male and median age at transplant was 13.4 years (interquartile range [IQR], 8.9-15.6) with a median follow-up of 35.2 months (IQR, 18.0-54.5). Incidence of CMV DNAemia within the first 3 months after prophylaxis cessation in CMV D + R- and CMV R+ children was 22.9% and 23.5% and incidence of CMV disease was 11.4% and 0%, respectively. Cumulative incidence of CMV DNAemia in both groups was similar (31.4%). Children who received antithymocyte globulin were more likely to develop CMV DNAemia compared with those who received anti-IL-2 (IRR, 2.98; 95% confidence interval, 1.41-6.30) after controlling for age, sex, Epstein-Barr Virus serostatus and rejection.
This study demonstrates a high incidence of CMV infection after cessation of antiviral prophylaxis. These results support extension of antiviral prophylaxis beyond 3 months and/or intensive viral load monitoring to reduce risk of CMV infection in D + R- and R+ children, especially those receiving antithymocyte globulin.
肾移植受者停止病毒预防治疗后可能会发生迟发性巨细胞病毒(CMV)感染,但感染的时间尚不清楚,可能需要更长时间的预防治疗。
我们对 2002 年 1 月至 2014 年 6 月期间接受肾移植的 86 名年龄均小于 18 岁的儿童(35 名 CMV 供者血清阳性、受者血清阴性[D + R-]和 51 名 CMV 受者血清阳性[R+])进行了回顾性队列研究,这些儿童在移植后接受了 3 个月的抗病毒预防治疗。使用 Kaplan-Meier 分析确定 CMV DNA 血症和 CMV 疾病的发生率,并使用泊松回归评估危险因素。
86 名儿童中,61.6%为男性,移植时的中位年龄为 13.4 岁(四分位距 [IQR],8.9-15.6),中位随访时间为 35.2 个月(IQR,18.0-54.5)。CMV D + R-和 CMV R+儿童在预防治疗停止后 3 个月内 CMV DNA 血症的发生率分别为 22.9%和 23.5%,CMV 疾病的发生率分别为 11.4%和 0%。两组的累积 CMV DNA 血症发生率相似(31.4%)。在控制年龄、性别、Epstein-Barr 病毒血清状态和排斥反应后,与接受抗白细胞介素-2 治疗的儿童相比,接受抗胸腺细胞球蛋白治疗的儿童更有可能发生 CMV DNA 血症(IRR,2.98;95%置信区间,1.41-6.30)。
本研究表明,抗病毒预防治疗停止后 CMV 感染的发生率较高。这些结果支持将抗病毒预防治疗延长至 3 个月以上和/或进行强化病毒载量监测,以降低 D + R-和 R+儿童发生 CMV 感染的风险,尤其是那些接受抗胸腺细胞球蛋白治疗的儿童。