成人实体器官移植受者 Epstein-Barr Virus DNA 血症的单中心治疗结果。

IF 0.9 Q3 SURGERY
Journal of Transplantation Pub Date : 2024-01-18 eCollection Date: 2024-01-01 DOI:10.1155/2024/5598324
Sara W Dong, Barbra M Blair, Carolyn D Alonso
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引用次数: 0

摘要

背景:实体器官移植(SOT)中的免疫抑制会增加爱泼斯坦-巴氏病毒(EBV)DNA血症的风险,这可能预示着移植后淋巴组织增生性疾病(PTLD)的发展。有关成人 SOT 受者(SOTR)中 EBV DNA 血症的发病率、风险因素和临床影响的研究很少:方法:对2015年1月1日至2019年12月31日期间的成人(≥18岁)SOT受者进行了单中心回顾性研究。根据患者出现EBV DNA血症(全血EBV DNA PCR > 200拷贝/毫升)这一主要研究终点对患者进行分层。次要终点包括PTLD的发展、免疫抑制(RIS)的减少、预防性疗法的使用以及全因死亡率:在 442 例成人 SOTR 中,主要移植器官为肾脏(258 例,58%)和肝脏(141 例,31.9%)。大多数受试者(430人,97%)的EB病毒血清状态被归类为中危(R+)。8名受试者(2%)属于高风险(供体(D+/R-)),4名受试者(1%)属于低风险(D-/R-)。EBV DNA血症的总发病率为4.1%(18/442),中位检测时间为14个月(3-60个月)。D+/R-受试者的DNA血症比例最高(37.5%;P < 0.001)。PTLD 的发生与 EBV DNA 血症密切相关,有 DNA 血症的患者为 3/18(16.7%),无 DNA 血症的患者为 3/424(0.7%)(p < 0.001)。所有患有PTLD的患者均接受了RIS和利妥昔单抗治疗:我们观察到,在我们的成人 SOTR 队列中,EBV D+/R- 血清状态和 EBV DNA 血症的持续发展是与 PTLD 的后续发展相关的高风险特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Single-Center Outcomes of Epstein-Barr Virus DNAemia in Adult Solid Organ Transplant Recipients.

Background: Immunosuppression in solid organ transplantation (SOT) increases the risk of Epstein-Barr virus (EBV) DNAemia, which may herald development of posttransplant lymphoproliferative disease (PTLD). Few studies have characterized the incidence, risk factors, and clinical impact of EBV DNAemia in adult SOT recipients (SOTR).

Methods: A single-center, retrospective review of adult (≥18 years) SOTR between 01 January 2015 and 31 December 2019 was conducted. Patients were stratified by the primary study endpoint of development of EBV DNAemia (whole blood EBV DNA PCR > 200 copies/mL). Secondary endpoints included development of PTLD, reduction in immunosuppression (RIS), use of pre-emptive therapy, and all-cause mortality.

Results: Among 442 adult SOTR, the predominant transplant organs were the kidney (258, 58%) and liver (141, 31.9%). EBV serostatus in most subjects (430, 97%) was classified as intermediate risk (R+). Eight subjects (2%) were high risk (donor (D+/R-), and 4 (1%) were low risk (D-/R-). The overall incidence of EBV DNAemia was 4.1% (18/442) with a median time to detection of 14 months (range 3-60). The highest proportion of DNAemia was observed in D+/R- subjects (37.5%; p < 0.001). Development of PTLD was significantly associated with EBV DNAemia and occurred in 3/18 patients with DNAemia (16.7%) vs. 3/424 (0.7%) without DNAemia (p < 0.001). All patients with PTLD were managed with RIS and rituximab.

Conclusion: We observed that EBV D+/R- serostatus and development of sustained EBV DNAemia were high risk features associated with subsequent development of PTLD in our cohort of adult SOTR.

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