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Human cytomegalovirus kinetics following institution of artesunate after hematopoietic stem cell transplantation.

机译:造血干细胞移植后建立青蒿琥酯后的人巨细胞病毒动力学。

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The anti-malaria drug artesunate has been shown to be an effective inhibitor of cytomegalovirus (CMV) in vitro, in an experimental animal model, and in a recent single-case clinical use. In this first case-series of 6 stem cell transplant recipients who received preemptive artesunate treatment for CMV infection, we have examined the viral kinetics following institution of artesunate, and employed first-phase viral kinetics studies to calculate its antiviral effectiveness. Two patients demonstrated a rapid 0.8-2.1 log viral load decline by 7 days, with a viral decay half-live of 0.9-1.9 days. Four patients demonstrated a continued yet stalled viral growth slope during treatment. No adverse events were noted in treatment courses of up to 28 days. Overall, a divergent antiviral efficacy was revealed, ranging from 43% to 90%, which appeared to be primarily dependent on the virus baseline growth dynamics. Further dose escalation studies are needed to examine the role of artesunate in the treatment of CMV infection in the transplantation setting.
机译:在体外,实验动物模型和最近的单例临床应用中,抗疟药青蒿琥酯已被证明是巨细胞病毒(CMV)的有效抑制剂。在这6名接受青蒿琥酯抢先治疗CMV感染的干细胞移植受者的第一个病例系列中,我们检查了青蒿琥酯治疗后的病毒动力学,并采用了第一阶段病毒动力学研究来计算其抗病毒效力。两名患者在7天后显示出0.8-2.1 log病毒载量快速下降,病毒衰老半衰期为0.9-1.9天。四名患者在治疗期间表现出持续但停滞的病毒生长斜率。长达28天的治疗过程中未发现不良事件。总体而言,显示出不同的抗病毒功效,范围从43%到90%,这似乎主要取决于病毒基线生长动态。需要进一步的剂量递增研究以检查青蒿琥酯在移植环境中在CMV感染治疗中的作用。

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