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埃博拉病毒预防和治疗的新兴靶点和新方法。

Emerging targets and novel approaches to Ebola virus prophylaxis and treatment.

机构信息

Division of Pharmaceutics, The University of Texas at Austin, College of Pharmacy, PHR 4.214D, 2409 W. University Ave., 1 University Station #A1920, Austin, TX, 78712-1074, USA.

出版信息

BioDrugs. 2013 Dec;27(6):565-83. doi: 10.1007/s40259-013-0046-1.

Abstract

Ebola is a highly virulent pathogen causing severe hemorrhagic fever with a high case fatality rate in humans and non-human primates (NHPs). Although safe and effective vaccines or other medicinal agents to block Ebola infection are currently unavailable, a significant effort has been put forth to identify several promising candidates for the treatment and prevention of Ebola hemorrhagic fever. Among these, recombinant adenovirus-based vectors have been identified as potent vaccine candidates, with some affording both pre- and post-exposure protection from the virus. Recently, Investigational New Drug (IND) applications have been approved by the US Food and Drug Administration (FDA) and phase I clinical trials have been initiated for two small-molecule therapeutics: anti-sense phosphorodiamidate morpholino oligomers (PMOs: AVI-6002, AVI-6003) and lipid nanoparticle/small interfering RNA (LNP/siRNA: TKM-Ebola). These potential alternatives to vector-based vaccines require multiple doses to achieve therapeutic efficacy, which is not ideal with regard to patient compliance and outbreak scenarios. These concerns have fueled a quest for even better vaccination and treatment strategies. Here, we summarize recent advances in vaccines or post-exposure therapeutics for prevention of Ebola hemorrhagic fever. The utility of novel pharmaceutical approaches to refine and overcome barriers associated with the most promising therapeutic platforms are also discussed.

摘要

埃博拉是一种高毒力病原体,可导致人类和非人类灵长类动物(NHPs)发生严重出血热,病死率高。尽管目前尚无安全有效的疫苗或其他药物来阻断埃博拉感染,但人们已经做出了巨大努力,以确定几种有希望的治疗和预防埃博拉出血热的候选药物。其中,重组腺病毒载体已被确定为有效的疫苗候选物,其中一些可提供针对病毒的预先和暴露后保护。最近,美国食品和药物管理局(FDA)已批准了两项新的研究性药物(IND)申请,并已启动了两种小分子治疗药物的 I 期临床试验:反义磷酸二酰胺吗啉寡聚物(PMO:AVI-6002、AVI-6003)和脂质纳米颗粒/小干扰 RNA(LNP/siRNA:TKM-Ebola)。这些基于载体的疫苗的潜在替代品需要多次给药才能达到治疗效果,这在患者依从性和疫情方面不理想。这些担忧促使人们寻求更好的疫苗接种和治疗策略。在这里,我们总结了最近在预防埃博拉出血热方面的疫苗或暴露后治疗方面的进展。还讨论了新型药物方法的实用性,以完善和克服最有前途的治疗平台相关的障碍。

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