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Artemisone demonstrates synergistic antiviral activity in combination with approved and experimental drugs active against human cytomegalovirus

机译:阿尔甲酮与批准的和实验药物联合患有针对人巨细胞病毒的协同抗病毒活动

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We have recently shown that the artemisinin derivative artemisone, which was screened against malaria in human clinical studies, is a potent inhibitor of human cytomegalovirus (HCMV). Here we evaluated the antiviral effect of artemisone when employed in 2-drug combinations with approved and experimental anti-HCMV agents. Using the Chou-Talalay method, we found that in-vitro combination of artemisone with cidofovir, brincidofovir, or with the HCMV UL97 inhibitor maribavir resulted in antiviral synergism and the combination of artemisone with ganciclovir or with the viral terminase inhibitors letermovir and BDCRB resulted in moderate synergism. Importantly, the combination of artemisone with maribavir demonstrated synergistic antiviral activity ex-vivo, in a clinically-relevant multicellular model of human placental tissues maintained in organ culture. Our findings provide the basis for the use of artemisone in synergistically acting drug combinations, to enhance viral control and reduce antiviral drug toxicities.
机译:我们最近表明,在人类临床研究中筛查疟疾的氨化蛋白衍生物蒿属植物是人巨细胞病毒(HCMV)的有效抑制剂。在这里,我们评估了在具有批准和实验性抗HCMV剂的2药物组合中使用时蒿酮的抗病毒作用。使用Chou-Talalay方法,我们发现与Cidofovir,Brincidofovir或HCMV UL97抑制剂Maribavir的体外组合导致抗病毒协同作用和与生命洛韦尔或病毒终止酶抑制剂Letermovir和BDCRB的组合中等协同作用。重要的是,在Maribavir与Maribavir的组合表明,在维持器官培养中的临床相关的多细胞模型中,在临床相关的人胎盘组织的多细胞模型中表现出协同抗病毒活性。我们的研究结果提供了在协同作用药物组合中使用蒿酮的基础,以提高病毒对照并减少抗病毒药物毒性。

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