Emerging Targets and Novel Approaches to Ebola Virus Prophylaxis and Treatment

被引:66
作者
Choi, Jin Huk [1 ]
Croyle, Maria A. [1 ,2 ]
机构
[1] Univ Texas Austin, Coll Pharm, Div Pharmaceut, Austin, TX 78712 USA
[2] Univ Texas Austin, Inst Cellular & Mol Biol, Austin, TX 78712 USA
基金
美国国家卫生研究院;
关键词
PROTECTS NONHUMAN-PRIMATES; MARBURG HEMORRHAGIC-FEVER; SMALL-MOLECULE INHIBITOR; NIEMANN-PICK C1; VACCINE PROTECTS; POSTEXPOSURE PROTECTION; GUINEA-PIGS; DELIVERY-SYSTEMS; ZAIRE-EBOLAVIRUS; DENDRITIC CELLS;
D O I
10.1007/s40259-013-0046-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:565 / 583
页数:19
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