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异基因造血细胞移植后腺病毒血症的病毒动力学和结果。

Viral kinetics and outcomes of adenovirus viremia following allogeneic hematopoietic cell transplantation.

机构信息

Division of Infectious Diseases and International Medicine, University of Minnesota, Minneapolis, Minnesota, USA.

Department of Pharmacy, Sylvester Comprehensive Cancer Center, Miami, Florida, USA.

出版信息

Clin Transplant. 2021 Dec;35(12):e14481. doi: 10.1111/ctr.14481. Epub 2021 Sep 28.

Abstract

BACKGROUND

Adenovirus (AdV) is a serious infection following hematopoietic cell transplantation (HCT). Little is known about AdV viral kinetics and optimal threshold for initiation of pre-emptive therapy.

METHODS

Single-center retrospective study of 16 consecutive adult HCT recipients with detectable AdV identified over a 5-year period.

RESULTS

Median time to AdV reactivation after HCT was 176 days (IQR 86-408). Nine patients received cidofovir, although 14/16 had no tissue-invasive disease. Among treated patients, median duration of viremia was shorter when initiating treatment at viral loads < 10,000 copies/ml (28 vs. 52 days). All-cause mortality in this cohort was 44%. All six patients (five of which were untreated) with peak viral loads < 10,000 copies/ml survived; whereas only 30% (3/10) of patients with peak viral loads greater than this threshold survived, despite most (n = 8; 80%) of them receiving cidofovir (P = .01). Three-month survival following diagnosis of AdV viremia was significantly lower with peak viremia > 10,000 copies/ml (100 vs. 17%; P = .005).

CONCLUSION

AdV is associated with high all-cause mortality, especially for viremia > 10,000 copies/ml. Delaying therapy until viremia reaches AdV levels ≥10,000 copies/ml was associated with more protracted infection and poor outcomes. Larger studies are needed.

摘要

背景

腺病毒(AdV)是造血细胞移植(HCT)后的严重感染。对于 AdV 病毒动力学和启动先发治疗的最佳阈值知之甚少。

方法

对 5 年内连续 16 例可检测到 AdV 的成年 HCT 受者进行单中心回顾性研究。

结果

HCT 后 AdV 再激活的中位时间为 176 天(IQR 86-408)。9 例患者接受了更昔洛韦治疗,尽管 14/16 例患者无组织侵袭性疾病。在接受治疗的患者中,当病毒载量<10000 拷贝/ml 时开始治疗,病毒血症的中位持续时间更短(28 天与 52 天)。该队列的全因死亡率为 44%。所有 6 例(其中 5 例未经治疗)峰值病毒载量<10000 拷贝/ml 的患者存活;而峰值病毒载量大于此阈值的患者中只有 30%(3/10)存活,尽管他们中的大多数(n=8;80%)接受了更昔洛韦治疗(P=0.01)。AdV 血症诊断后,峰值病毒载量>10000 拷贝/ml 的患者 3 个月生存率显著降低(100%与 17%;P=0.005)。

结论

AdV 与全因死亡率高相关,尤其是病毒载量>10000 拷贝/ml 时。延迟治疗至病毒载量达到 AdV 水平≥10000 拷贝/ml 与感染时间延长和预后不良相关。需要更大规模的研究。

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