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Gene-Specific Countermeasures against Ebola Virus Based on Antisense Phosphorodiamidate Morpholino Oligomers

机译:基于反义磷酸二酰胺吗啉代寡聚物的埃博拉病毒基因特异性对策

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摘要

The filoviruses Marburg virus and Ebola virus (EBOV) quickly outpace host immune responses and cause hemorrhagic fever, resulting in case fatality rates as high as 90% in humans and nearly 100% in nonhuman primates. The development of an effective therapeutic for EBOV is a daunting public health challenge and is hampered by a paucity of knowledge regarding filovirus pathogenesis. This report describes a successful strategy for interfering with EBOV infection using antisense phosphorodiamidate morpholino oligomers (PMOs). A combination of EBOV-specific PMOs targeting sequences of viral mRNAs for the viral proteins (VPs) VP24, VP35, and RNA polymerase L protected rodents in both pre- and post-exposure therapeutic regimens. In a prophylactic proof-of-principal trial, the PMOs also protected 75% of rhesus macaques from lethal EBOV infection. The work described here may contribute to development of designer, “druggable” countermeasures for filoviruses and other microbial pathogens.
机译:线状病毒马尔堡病毒和埃博拉病毒(EBOV)迅速超过宿主的免疫反应并引起出血热,导致人类的病死率高达90%,非人类的灵长类动物高达近100%。有效的EBOV治疗药物的开发是一项艰巨的公共卫生挑战,并且由于缺乏有关丝状病毒发病机理的知识而受到阻碍。该报告描述了使用反义二氨基磷酸二氨基吗啉代寡聚物(PMO)干扰EBOV感染的成功策略。在暴露前和暴露后的治疗方案中,针对病毒蛋白(VPs)VP24,VP35和RNA聚合酶L的EBOV特异性PMO靶向病毒mRNA序列的组合。在一项预防性原则证明试验中,PMO还保护了75%的猕猴免受致命性EBOV感染。此处描述的工作可能有助于开发针对丝状病毒和其他微生物病原体的设计者,“可吸收”的对策。

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