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Ebola virus (EBOV) infection: Therapeutic strategies

机译:埃博拉病毒(EBOV)感染:治疗策略

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Within less than a year after its epidemic started (in December 2013) in Guinea, Ebola virus (EBOV), a member of the filoviridae, has spread over a number of West-African countries (Guinea, Sierra Leone and Liberia) and gained allures that have been unprecedented except by human immunodeficiency virus (HIV). Although EBOV is highly contagious and transmitted by direct contact with body fluids, it could be counteracted by the adequate chemoprophylactic and -therapeutic interventions: vaccines, antibodies, siRNAs (small interfering RNAs), interferons and chemical substances, i.e. neplanocin A derivatives (i.e. 3-deazaneplanocin A), BCX4430, favipiravir (T-705), endoplasmic reticulum (ER) alpha-glucosidase inhibitors and a variety of compounds that have been found to inhibit EBOV infection blocking viral entry or by a mode of action that still has to be resolved. Much has to be learned from the mechanism of action of the compounds active against VSV (vesicular stomatitis virus), a virus belonging to the rhabdoviridae, that in its mode of replication could be exemplary for the replication of filoviridae. (C) 2014 Elsevier Inc. All rights reserved.
机译:几内亚流行的埃博拉病毒(EBOV)在几内亚开始流行后不到一年(2013年12月),已传播到许多西非国家(几内亚,塞拉利昂和利比里亚),并获得了吸引力除了人类免疫缺陷病毒(HIV)以外,这是前所未有的。尽管EBOV具有高度传染性,并通过与体液直接接触而传播,但可以通过适当的化学预防和治疗干预措施来抵消:疫苗,抗体,siRNA(小干扰RNA),干扰素和化学物质,例如奈普罗辛A衍生物(即3 -deazaneplanocin A),BCX4430,favipiravir(T-705),内质网(ER)α-葡萄糖苷酶抑制剂和多种化合物已被发现能够抑制EBOV感染从而阻止病毒进入或通过仍然需要的作用方式解决。从对属于横纹病毒科的病毒VSV(水泡性口炎病毒)有活性的化合物的作用机理中必须学到很多,以其复制方式可以作为丝状病毒科复制的示例。 (C)2014 Elsevier Inc.保留所有权利。

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