Centre for Virology, Department of Infection, UCL London, United Kingdom.
J Clin Virol. 2010 Sep;49(1):32-6. doi: 10.1016/j.jcv.2010.06.018. Epub 2010 Jul 27.
Cytomegalovirus (HCMV) remains an important infection following stem cell transplantation (SCT) and is managed via pre-emptive therapy. In some patients HCMV loads continue to increase after therapy and they experience multiple episodes of replication.
To identify the risk factors associated with failure to immediately control HCMV replication after antiviral therapy and for recurrence of replication.
Replication kinetics of human cytomegalovirus (HCMV) were studied a cohort of 153 T-cell depleted allogeneic SCT patients.
In 57 patients (31%) who experienced HCMV DNAemia, the mean growth rate of HCMV was 0.35 day(-1) equivalent to a doubling time of 2.2 days. In patients requiring anti-HCMV treatment with either ganciclovir or ganciclovir/foscarnet (n=49), HCMV load increased to a peak value of >2 days after initiation of therapy in 21 patients and only the growth rate prior to therapy was a risk factor (Odds ratio=1.4 per 0.1 day(-1) increase; p=0.004). In patients where antiviral intervention occurred after peak virus load the decline rate of HCMV load was accelerated 4-fold if the patient was subsequently initiated on anti-HCMV therapy (p=0.02). A subset of patients (38%) experienced a recurrence of their DNAemia at a mean of 20 days after the cessation of their first replication episode and this was only associated with receiving stem cells from a seronegative donor (Odds ratio=6.59; p<0.001).
The kinetics of response to therapy is closely associated with HCMV replication kinetics prior to therapy while recurrence of replication is associated with HCMV serostatus of the donor.
巨细胞病毒(HCMV)在干细胞移植(SCT)后仍然是一种重要的感染,通过抢先治疗进行管理。在一些患者中,HCMV 负荷在治疗后继续增加,并且经历多次复制。
确定与抗病毒治疗后不能立即控制 HCMV 复制以及复制复发相关的危险因素。
研究了一组 153 例 T 细胞耗尽的同种异体 SCT 患者的人类巨细胞病毒(HCMV)复制动力学。
在 57 例(31%)发生 HCMV DNA 血症的患者中,HCMV 的平均增长率为 0.35 天(相当于倍增时间为 2.2 天)。在需要用更昔洛韦或更昔洛韦/膦甲酸钠进行抗 HCMV 治疗的 49 例患者中,21 例患者在开始治疗后 HCMV 负荷增加到峰值超过 2 天,只有治疗前的增长率是一个危险因素(优势比=每增加 0.1 天(-1)增加 1.4;p=0.004)。在病毒负荷峰值后进行抗病毒干预的患者中,如果随后开始抗 HCMV 治疗,则 HCMV 负荷的下降速度加快 4 倍(p=0.02)。一组患者(38%)在第一次复制发作停止后平均 20 天出现 DNA 血症复发,这仅与接受来自血清阴性供体的干细胞有关(优势比=6.59;p<0.001)。
治疗反应的动力学与治疗前的 HCMV 复制动力学密切相关,而复制的复发与供体的 HCMV 血清状态有关。