儿童单倍体干细胞移植中的巨细胞病毒感染。

Abdulrahman AlSweed, Suliman Aljumaah, Hawazen AlSaedi, Hibah Alruwaisan, Raghad Alhuthil, Sami Al-Hajjar
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引用次数: 0

摘要

背景:人巨细胞病毒(CMV)是儿童造血干细胞移植(HSCT)发病和死亡的主要来源。巨细胞病毒的复制主要受t细胞介导的免疫控制。尽管接受了治疗,巨细胞病毒再激活仍然对移植后的预后有显著的不利影响。在这项研究中,我们研究了CMV再激活和疾病的临床方面和危险因素,以及治疗干预对接受HSCT的儿科患者的影响。方法:这项回顾性的单中心研究纳入了2013年至2018年在沙特阿拉伯利雅得费萨尔国王专科医院和研究中心接受单倍体造血干细胞移植的儿科患者。结果:共纳入94例HSCT受者:女性46例(48.94%),男性48例(51.06%),中位年龄为5岁[四分位数间距(IQR): 1.2-8.7]。献血者中男性57例(60.64%),女性37例(39.36%),中位年龄30.7岁(IQR: 23.0 ~ 35.3)。52例(55.32%)HSCT患者发生巨细胞病毒再激活。总死亡率为12.77%(12/94),其中83.33%(10/12)为CMV阳性。然而,没有患者发生巨细胞病毒肺炎、胃炎或结肠炎,巨细胞病毒未被确定为直接死亡原因。在CMV危险因素方面,较高的受体年龄和存在急性移植物抗宿主病与CMV再激活显著相关(P < 0.05)。结论:预防巨细胞病毒感染对移植后的病程有显著影响,特别是在供体不匹配的情况下。本研究表明,通过先发制人的治疗预防巨细胞病毒的检出率为78.85%。目前以聚合酶链反应(PCR)为指导的监测和预防已经降低了巨细胞病毒疾病和持续性dna血症的发生率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytomegalovirus infection in pediatric haploidentical stem cell transplantation.

Background: Human cytomegalovirus (CMV) is a major source of morbidity and mortality in pediatric hematopoietic stem cell transplantation (HSCT). CMV replication is mainly controlled by T-cell-mediated immunity. Despite treatment, CMV reactivation continues to have a significant adverse impact on post-transplant outcomes. In this study, we examine the clinical aspects and risk factors for CMV reactivation and disease, and the effect of therapeutic interventions in pediatric patients who underwent HSCT.

Methods: This retrospective, single-center study included pediatric patients who underwent haploidentical HSCT at King Faisal Specialist Hospital and Research Center in Riyadh, Saudi Arabia, from 2013 to 2018.

Results: A total of 94 HSCT recipients were included: 46 (48.94%) females and 48 (51.06%) males, with a median age of 5 years [interquartile range (IQR): 1.2-8.7]. As for donors, 57 (60.64%) were males and 37 (39.36%) were females, with a median age of 30.7 years (IQR: 23.0-35.3). CMV reactivation occurred in 52 (55.32%) of the HSCT patients. The overall mortality rate was 12.77% (12/94), and of those, 83.33% (10/12) were CMV positive. However, no patient developed CMV pneumonitis, gastritis, or colitis, and CMV was not identified as the direct cause of death. Regarding CMV risk factors, higher recipient age and the presence of acute graft-versus-host disease were significantly associated with CMV reactivation (P < 0.05).

Conclusion: Preventing CMV infection significantly impacts the post-transplant course, especially in the setting of mismatched donors. This study showed that preventing CMV by preemptive therapy revealed an undetectable rate of 78.85%. Current polymerase chain reaction (PCR)-directed surveillance and prophylaxis have lowered the incidence of CMV disease and persistent DNAemia.

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