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血清阴性实体器官移植受者接受血清阴性供体器官后发生的输血传播和社区获得性巨细胞病毒感染。

Transfusion-transmitted and community-acquired cytomegalovirus infection in seronegative solid organ transplant recipients receiving seronegative donor organs.

机构信息

Department of Pediatrics, University of Alberta, Edmonton, Alberta, Canada.

Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.

出版信息

Am J Transplant. 2020 Dec;20(12):3509-3519. doi: 10.1111/ajt.16066. Epub 2020 Jun 11.

DOI:10.1111/ajt.16066
PMID:32428296
Abstract

Solid organ transplant (SOT) recipients who are cytomegalovirus (CMV) seronegative (R-) and receive seronegative donor (D-) organs have a small but currently unquantified risk of both transfusion-transmitted CMV (TT-CMV) and community-acquired CMV (CA-CMV). We retrospectively studied the incidence and clinical symptoms of TT-CMV (infection <1 year posttransplant) and CA-CMV (infection >1 year posttransplant) in a cohort of D-/R- adult and pediatric SOT recipients receiving leukoreduced blood products not screened for CMV seronegativity transplanted at our center between 2000 and 2011. CMV infection was defined as IgG seroconversion or detectable CMV antigenemia/DNAemia. Among 536 consecutive D-/R- recipients, 398 (81.8%) had adequate follow-up, and 231 (58%) received cellular blood products (total: 1626 red blood cell units, 470 platelet units) 30 days pretransplant to 90 days posttransplant. We observed no confirmed TT-CMV cases, but 14 CA-CMV cases (64% symptomatic) were seen. The estimated incidence rate of CA-CMV was higher in children (3.0/100 patient years) than adults (0.46/100 patient years, incident rate ratio of 6.52). The absence of TT-CMV over 11 years suggests neither seronegative blood products nor CMV DNA blood donor screening would provide significant incremental safety when blood is already leukoreduced. D-/R- SOT recipients, particularly children, have a significantly higher and ongoing risk of CA-CMV.

摘要

实体器官移植(SOT)受者为巨细胞病毒(CMV)阴性(R-),接受阴性供体(D-)器官,存在较小但目前无法量化的输血传播 CMV(TT-CMV)和社区获得性 CMV(CA-CMV)的风险。我们回顾性研究了在本中心 2000 年至 2011 年间接受白细胞减少血液制品(未筛选 CMV 阴性)移植的 D-/R-成年和儿科 SOT 受者队列中 TT-CMV(移植后 1 年内感染)和 CA-CMV(移植后 1 年以上感染)的发生率和临床症状。CMV 感染定义为 IgG 血清转化或可检测到 CMV 抗原血症/DNA 血症。在 536 例连续 D-/R-受者中,398 例(81.8%)有足够的随访,231 例(58%)在移植前 30 天至移植后 90 天接受细胞血液制品(共 1626 单位红细胞,470 单位血小板)。我们未观察到确诊的 TT-CMV 病例,但发现 14 例 CA-CMV 病例(64%有症状)。儿童的 CA-CMV 发病率(3.0/100 患者年)高于成人(0.46/100 患者年,发病率比为 6.52)。11 年以上无 TT-CMV 表明,即使血液已经白细胞减少,阴性血液制品或 CMV DNA 血液供体筛查也不会提供显著的额外安全性。D-/R- SOT 受者,特别是儿童,CA-CMV 的风险显著更高且持续存在。

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引用本文的文献

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2
Cytomegalovirus in the transplant setting: Where are we now and what happens next? A report from the International CMV Symposium 2021.移植环境中的巨细胞病毒:我们现在在哪里,下一步会发生什么?来自 2021 年国际巨细胞病毒研讨会的报告。
Transpl Infect Dis. 2022 Dec;24(6):e13977. doi: 10.1111/tid.13977. Epub 2022 Nov 11.