Significance of Asymptomatic Persistent Epstein-Barr Viral Load in Pediatric Renal Transplant Recipients: North American Pediatric Renal Trials and Collaborative Studies Report

A. Moudgil, K. Martz, Therese Moore, W. Harmon, V. Dharnidharka
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引用次数: 7

Abstract

Background: Many pediatric transplant (TX) centers routinely monitor Epstein-Barr (EB) viral load (VL) by real time quantitative PCR and intervene to prevent post-transplant lymphoproliferative disorder (PTLD). Some children develop asymptomatic persistent VL (PVL). Outcome of different interventions in preventing PTLD and other undesired effects on acute rejection (AR), graft failure (GF) and function amongst children with asymptomatic PVL is not known. Methods: NAPRTCS centers invited to enter data on children with asymptomatic PVL (≥ 6 months) into the EB VL registry. Comparison group included children into the NAPRTCS TX arm during the same period without PVL or VL monitoring. EB VL were arbitrarily divided into low (1-10), medium (>10-100) and high (>100times detection limit for the center) ratio. Results: Of 645 children (18 centers), 85 (13.2%) developed onset of PVL at a mean of 6.4 ± 6.3 months post-TX. PVL children were more likely to be younger (< 5 years) at TX and less likely to be African-American and majority (75.3%) was mismatched for EBV (donor EBV IgG positive and recipient negative). Thymoglobulin induction was used in 29.4% children with PVL versus 37% in controls (p=ns). PTLD developed in 7/85 (8.2%) children with PVL versus 5/560 (0.9%) controls (p < 0.0001). EB VL ratios were not different in those with and without PTLD. EB PVL as time varying covariate did not affect patient survival, GF and AR (HR, 0.85, 0.53 and 0.99). The change in GFR overtime in children with PVL was comparable to controls. Conclusion: Children with PVL (actual load not predictive) are at increased risk for PTLD, but not for AR, death, GF or loss of graft function.
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儿童肾移植受者无症状持续性Epstein-Barr病毒载量的意义:北美儿童肾脏试验和合作研究报告
背景:许多儿科移植(TX)中心通过实时定量PCR监测EB病毒载量(VL),并干预预防移植后淋巴细胞增生性疾病(PTLD)。一些儿童发展为无症状的持续性VL (PVL)。在无症状PVL儿童中,预防PTLD和其他对急性排斥反应(AR)、移植物衰竭(GF)和功能的不良影响的不同干预措施的结果尚不清楚。方法:邀请NAPRTCS中心将无症状PVL(≥6个月)儿童的数据输入EB VL登记处。对照组在同一时期将儿童纳入NAPRTCS TX组,无PVL或VL监测。将ebvl随机分为低(1-10)、中(>10-100)和高(>100倍检测限为中心)比率。结果:645名儿童(18个中心)中,85名(13.2%)在tx后平均6.4±6.3个月发生PVL。PVL儿童在TX时更可能年龄更小(< 5岁),非裔美国人的可能性更小,大多数(75.3%)EBV不匹配(供体EBV IgG阳性,受体EBV IgG阴性)。29.4%的PVL患儿使用胸腺球蛋白诱导治疗,而对照组为37% (p=ns)。PVL患儿中有7/85(8.2%)发生PTLD,对照组为5/560 (0.9%)(p < 0.0001)。有无PTLD的EB - VL比值无显著差异。ebpvl作为时变协变量对患者生存、GF和AR无影响(HR分别为0.85、0.53和0.99)。PVL患儿GFR随时间的变化与对照组相当。结论:PVL患儿(实际负荷不可预测)发生PTLD的风险增加,但发生AR、死亡、GF或移植物功能丧失的风险没有增加。
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7
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