小儿肝移植受者感染爱泼斯坦巴氏病毒和巨细胞病毒的经验:2014-2017 年研究

Paola Marsela Pérez Camacho , Jaime Alberto Patiño-Niño , Lina María Jaimes , María Camila López-Girón , Laura Torres-Canchala , Víctor García-Montoya , Camila Ariza-Insignares , Lina M. Sandoval-Calle , Inés E. Gómez , Mario Bustos-Paz , Luis Armando Caicedo , Verónica Botero-Osorio
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引用次数: 0

摘要

导言本研究介绍了我们在小儿肝移植人群中发现的爱泼斯坦巴氏病毒(EBV)和巨细胞病毒(CMV)感染及其与移植后淋巴细胞增生综合征(PTLD)发生的潜在关联。患者和方法这项回顾性描述性研究的时间跨度为2014年至2017年,研究对象包括在移植后第一年接受EVB和CMV病毒载量监测的小儿肝移植受者。结果研究共纳入89名患者,中位年龄为0.68岁(RIQ 0.31-0.96)(10.8个月RIQ 8.4-25.2)。导致移植的最常见的基础病变是胆道闭锁,有 55 例(61.6%)。在 EBV 病毒载量方面,移植后 3 个月时超过 10,000 拷贝/毫升的患者有 9 人(8%),6 个月时有 33 人(29.3%),9 个月时有 31 人(27.6%),12 个月时有 25 人(22.3%)。移植后一年内感染 EBV 的概率为 81.3%,感染 CMV 的概率为 29%。共有 8 例(8.9%)活检证实发生移植物排斥,其中只有 1 例为 EBV 和 CMV 阴性。EB病毒感染者发生移植物排斥反应的可能性为21.5%,CMV感染者为20.8%。重要的是,在12个月的随访期间,仅记录到一例PTLD病例。结论对这一小儿肝移植人群进行特征描述并监测EBV和CMV病毒载量,可以及时采取干预措施,从而降低PTLD和移植物排斥反应的风险。
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Experience with Epstein barr virus and Cytomegalovirus infection in pediatric liver transplant recipients: A 2014–2017 study

Introduction

This study presents our experience with Epstein Barr virus (EBV) and Cytomegalovirus (CMV) infections in the pediatric liver transplant population and their potential association with the development of the post-transplant lymphoproliferative syndrome (PTLD).

Patients and methods

This retrospective descriptive study covers the period from 2014 to 2017 and includes pediatric liver transplanted recipients who underwent viral load monitoring for EVB and CMV during the first-year post-transplant.

Results

A total of 89 patients were included in the study, with a median age of 0.68 years (RIQ 0.31–0.96) (10.8 months RIQ 8.4–25.2). The most common underlying pathology leading to transplantation was biliary atresia, observed in 55 (61.6 %) cases. Regarding EBV viral loads, values exceeding 10,000 copies/ml were observed in 9 (8 %) patients at 3 months, 33 (29.3 %) at 6 months, 31 (27.6 %) at 9 months and 25 (22.3 %) at 12 months post-transplantation. The probability of developing EBV infection within one-year post-transplantation was 81.3 %, while the probability of CMV infection was 29 %. A total of 8 (8.9 %) biopsy-confirmed graft rejections occurred, only 1 was EBV and CMV-negative. The likelihood of graft rejection in patients with EBV infection was 21.5 %, and for CMV it was 20.8 %. Importantly, only one case of PTLD was documented during 12 months follow-up.

Conclusion

Characterizing this pediatric liver transplant population and monitoring EBV and CMV viral loads enables timely interventions, potentially reducing the risk of PTLD and graft rejection.

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