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移植后不久,巨细胞病毒(CMV)血症风险与供者来源造血干细胞移植后受者的血浆中 torque teno 病毒(TTV)DNA 载量动力学有关。

The kinetics of torque teno virus plasma DNA load shortly after engraftment predicts the risk of high-level CMV DNAemia in allogeneic hematopoietic stem cell transplant recipients.

机构信息

Microbiology Service, Hospital Clínico Universitario, Institute for Research INCLIVA, Valencia, Spain.

Hematology Service, Hospital Clínico Universitario, Institute for Research INCLIVA, Valencia, Spain.

出版信息

Bone Marrow Transplant. 2018 Feb;53(2):180-187. doi: 10.1038/bmt.2017.235. Epub 2017 Oct 30.

Abstract

Monitoring Torque teno virus (TTV) DNA load helps to estimate the risk of opportunistic infections in solid organ transplant recipients. We investigated whether the early kinetic pattern of plasma TTV DNA load after allogeneic hematopoietic stem cell transplantation (allo-HSCT) associates with subsequent CMV and EBV DNAemia. This study included 71 allo-HSCT patients. We found that the area under the curve (AUC) for log TTV DNA loads quantified by days 20 and 30 after transplantation (TTV DNA load AUC), was significantly lower (P=0.036) in patients who subsequently developed CMV DNAemia requiring preemptive antiviral therapy (n=17) than in those who did not (n=8) or had no CMV DNAemia (n=19). Patients displaying TTV DNA load AUC⩽2.8 copies × days × mL were more likely to have high-level CMV DNAemia. A trend towards a direct correlation between TTV DNA AUC and CMV-specific interferon-γ CD8+ T-cell counts by day +30 was noted (P=0.095). However, this dynamic parameter was not useful for anticipating the occurrence of either CMV recurrences (n=12) or EBV DNAemia (n=34). In summary, it may be possible to identify a subset of allo-HSCT patients at a high risk of developing high-level CMV DNAemia by analyzing the kinetics of plasma TTV DNA load early after engraftment.

摘要

监测扭结瘤病毒(TTV)DNA 载量有助于评估实体器官移植受者发生机会性感染的风险。我们研究了异基因造血干细胞移植(allo-HSCT)后血浆 TTV DNA 载量的早期动力学模式是否与随后的 CMV 和 EBV DNA 血症相关。这项研究纳入了 71 例 allo-HSCT 患者。我们发现,移植后第 20 天和第 30 天定量的 TTV DNA 载量的曲线下面积(TTV DNA 载量 AUC)在随后发生需要抢先抗病毒治疗的 CMV DNA 血症(n=17)的患者中明显低于未发生 CMV DNA 血症(n=8)或未发生 CMV DNA 血症(n=19)的患者(P=0.036)。TTV DNA 载量 AUC ⩽2.8 拷贝×天×毫升的患者更有可能发生高水平 CMV DNA 血症。TTV DNA AUC 与移植后第 30 天的 CMV 特异性干扰素-γ CD8+ T 细胞计数之间存在直接相关性的趋势(P=0.095)。然而,该动态参数对于预测 CMV 复发(n=12)或 EBV DNA 血症(n=34)的发生均无意义。总之,通过分析移植后早期血浆 TTV DNA 载量的动力学,可能可以识别出一组 allo-HSCT 患者发生高水平 CMV DNA 血症的风险较高。

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