• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

异基因造血细胞移植中的巨细胞病毒(CMV)管理:移植前预测生存、病毒再激活和自发清除。

Cytomegalovirus (CMV) management in allogeneic hematopoietic cell transplantation: Pre-transplant predictors of survival, reactivation, and spontaneous clearance.

机构信息

Haematology Department, Royal North Shore Hospital, Sydney, Australia.

National Centre for Infection in Cancer, Peter MacCallum Cancer Centre, Melbourne, Australia.

出版信息

Transpl Infect Dis. 2021 Jun;23(3):e13548. doi: 10.1111/tid.13548. Epub 2021 Jan 5.

DOI:10.1111/tid.13548
PMID:33342000
Abstract

BACKGROUND

Cytomegalovirus (CMV) reactivation is a frequent complication after allogeneic hematopoietic cell transplant (alloHCT).

METHOD

We analyzed 159 alloHCT recipients with 4409 quantitative CMV viral loads to determine pre-transplant predictors of CMV reactivation, clinically significant CMV infection (cs-CMVi, defined as CMV viral load >1000 IU/mL), CMV disease, kinetics of spontaneous clearance of CMV, and survival using a standardized pre-emptive therapy approach to identify at-risk groups to target prevention strategies.

RESULTS

Cs-CMVi was most common in D-/R+ unrelated donor transplants (URD). Spontaneous CMV clearance occurred in 26% of patients who reached a viral load of 56-137 IU/mL, 6% at 138-250 IU/mL and in one patient >250 IU/mL. Median time between the first CMV reactivation (>56 IU/mL) and a viral load >250 IU/mL was 13 days, whereas the time from the first viral load >250 IU/mL to reach a vial load >1000 IU/mL was 4 days. Cs-CMVi was associated with a significant increase in non-relapse mortality (NRM) on multivariate analysis.

CONCLUSIONS

Overall, this study indicates that D-/R+ URD recipients are at high-risk for cs-CMVi- and CMV-related mortality, and are potential candidates for targeted CMV prophylaxis. Spontaneous clearance of CMV beyond a viral load of 250 IU/mL is uncommon, suggesting that this could be used as an appropriate threshold to initiate pre-emptive therapy.

摘要

背景

巨细胞病毒(CMV)再激活是异基因造血细胞移植(alloHCT)后常见的并发症。

方法

我们分析了 159 例 alloHCT 受者的 4409 份定量 CMV 病毒载量,以确定 CMV 再激活、临床显著 CMV 感染(cs-CMVi,定义为 CMV 病毒载量>1000 IU/mL)、CMV 疾病、CMV 自发性清除动力学和生存的移植前预测因子,采用标准化的先发制人治疗方法确定高危人群,以确定预防策略的目标。

结果

D-/R+无关供体移植(URD)中最常见 cs-CMVi。26%达到 56-137 IU/mL 病毒载量的患者出现自发性 CMV 清除,6%达到 138-250 IU/mL 的患者出现自发性 CMV 清除,1 例患者>250 IU/mL。首次 CMV 再激活(>56 IU/mL)与病毒载量>250 IU/mL 之间的中位时间为 13 天,而从首次病毒载量>250 IU/mL 到病毒载量>1000 IU/mL 的时间为 4 天。多变量分析显示,cs-CMVi 与非复发死亡率(NRM)显著增加相关。

结论

总体而言,本研究表明 D-/R+URD 受者 cs-CMVi 和与 CMV 相关的死亡率风险高,是靶向 CMV 预防的潜在候选者。病毒载量>250 IU/mL 后 CMV 的自发性清除并不常见,这表明这可能作为启动先发制人治疗的适当阈值。

相似文献

1
Cytomegalovirus (CMV) management in allogeneic hematopoietic cell transplantation: Pre-transplant predictors of survival, reactivation, and spontaneous clearance.异基因造血细胞移植中的巨细胞病毒(CMV)管理:移植前预测生存、病毒再激活和自发清除。
Transpl Infect Dis. 2021 Jun;23(3):e13548. doi: 10.1111/tid.13548. Epub 2021 Jan 5.
2
Analysis of spontaneous cytomegalovirus clearance after low level reactivation using a pre-emptive treatment threshold of 4,000 IU/mL in allogeneic hematopoietic cell transplant recipients.分析异基因造血细胞移植受者采用 4,000IU/mL 抢先治疗阈值时的低水平再激活后自发巨细胞病毒清除情况。
J Infect Chemother. 2024 Dec;30(12):1233-1236. doi: 10.1016/j.jiac.2024.05.010. Epub 2024 May 28.
3
The Ability of a Cytomegalovirus ELISPOT Assay to Predict Outcome of Low-Level CMV Reactivation in Hematopoietic Cell Transplant Recipients.巨细胞病毒 ELISPOT 检测在预测造血细胞移植受者低水平 CMV 再激活结局中的作用。
J Infect Dis. 2019 Feb 23;219(6):898-907. doi: 10.1093/infdis/jiy592.
4
Impact of Cytomegalovirus Viral Load on Probability of Spontaneous Clearance and Response to Preemptive Therapy in Allogeneic Stem Cell Transplantation Recipients.巨细胞病毒病毒载量对异基因造血干细胞移植受者自发清除率和抢先治疗反应的影响。
Biol Blood Marrow Transplant. 2018 Apr;24(4):806-814. doi: 10.1016/j.bbmt.2017.11.038. Epub 2017 Dec 5.
5
Effective CMV prophylaxis with high-dose valaciclovir in allogeneic hematopoietic stem-cell recipients at a high risk of CMV infection.对巨细胞病毒(CMV)感染高危的异基因造血干细胞移植受者,采用高剂量伐昔洛韦进行有效的CMV预防。
Transpl Infect Dis. 2023 Feb;25(1):e13994. doi: 10.1111/tid.13994. Epub 2022 Dec 1.
6
Cytomegalovirus pre-emptive therapy after hematopoietic stem cell transplantation in the era of real-time quantitative PCR: comparison with recipients of solid organ transplants.实时定量聚合酶链反应时代造血干细胞移植后巨细胞病毒抢先治疗:与实体器官移植受者的比较
Transpl Infect Dis. 2016 Jun;18(3):405-14. doi: 10.1111/tid.12542. Epub 2016 Jun 9.
7
Cytomegalovirus (CMV) Cell-Mediated Immunity and CMV Infection After Allogeneic Hematopoietic Cell Transplantation: The REACT Study.巨细胞病毒(CMV)细胞介导免疫和异基因造血细胞移植后 CMV 感染:REACT 研究。
Clin Infect Dis. 2020 Dec 3;71(9):2365-2374. doi: 10.1093/cid/ciz1210.
8
Cytomegalovirus load at treatment initiation is predictive of time to resolution of viremia and duration of therapy in hematopoietic cell transplant recipients.造血细胞移植受者治疗开始时的巨细胞病毒载量可预测病毒血症消退时间及治疗持续时间。
J Clin Virol. 2015 Aug;69:179-83. doi: 10.1016/j.jcv.2015.06.006. Epub 2015 Jun 10.
9
Time to initiation of pre-emptive therapy for cytomegalovirus impacts overall survival in pediatric hematopoietic stem cell transplant recipients.抢先治疗巨细胞病毒的时机对儿科造血干细胞移植受者的总生存时间有影响。
Cytotherapy. 2022 Apr;24(4):428-436. doi: 10.1016/j.jcyt.2021.10.002. Epub 2022 Jan 15.
10
Letermovir for pre-emptive cytomegalovirus therapy after allogeneic hematopoietic cell transplantation.更昔洛韦用于异基因造血细胞移植后抢先性巨细胞病毒治疗。
Transpl Infect Dis. 2023 Nov;25 Suppl 1:e14147. doi: 10.1111/tid.14147. Epub 2023 Sep 7.

引用本文的文献

1
Seeing the Bigger Picture: Cytomegalovirus Retinitis Screening in Pediatric Hematopoietic Stem Cell Transplant Patients.着眼大局:儿童造血干细胞移植患者的巨细胞病毒性视网膜炎筛查
Pediatr Blood Cancer. 2025 Jul 18:e31910. doi: 10.1002/pbc.31910.
2
[Reactivation of cytomegalovirus and its influencing factors in patients with B-lymphocyte malignancy after CAR-T cell therapy].[CAR-T细胞治疗后B淋巴细胞恶性肿瘤患者巨细胞病毒再激活及其影响因素]
Zhonghua Xue Ye Xue Za Zhi. 2024 Nov 14;45(11):1005-1009. doi: 10.3760/cma.j.cn121090-20240703-00249.
3
Cytomegalovirus viral load at initiation of pre-emptive antiviral therapy impacts cytomegalovirus dynamics in pediatric allogeneic hematopoietic cell transplantation recipients.
抢先抗病毒治疗开始时的巨细胞病毒载量影响儿童异基因造血细胞移植受者的巨细胞病毒动态变化。
Transpl Infect Dis. 2024 Dec;26(6):e14358. doi: 10.1111/tid.14358. Epub 2024 Aug 26.
4
CMV reactivation during pretransplantation evaluation: a novel risk factor for posttransplantation CMV reactivation.移植前评估期间的 CMV 再激活:移植后 CMV 再激活的一个新的危险因素。
Blood Adv. 2024 Sep 10;8(17):4568-4580. doi: 10.1182/bloodadvances.2023012234.
5
Optimizing Access to Unrelated Donors in Canada: Re-Examining the Importance of Donor Factors on Outcomes Following Hematopoietic Cell Transplantation.优化加拿大非亲属供者的获取途径:重新审视供者因素对造血细胞移植后结局的重要性。
Curr Oncol. 2024 Apr 30;31(5):2542-2551. doi: 10.3390/curroncol31050190.
6
Genetic variants associated with cytomegalovirus infection after allogeneic hematopoietic cell transplantation.与异基因造血细胞移植后巨细胞病毒感染相关的遗传变异。
Blood. 2021 Oct 28;138(17):1628-1636. doi: 10.1182/blood.2021012153.