Acosta Eliana G, Bartenschlager Ralf
Department of Infectious Diseases, Molecular Virology, Heidelberg University, Heidelberg, Germany.
Department of Infectious Diseases, Molecular Virology, Heidelberg University, Heidelberg, Germany; German Center for Infection Research (DZIF), Partner-site Heidelberg, Germany.
Curr Opin Virol. 2016 Oct;20:47-54. doi: 10.1016/j.coviro.2016.09.003. Epub 2016 Sep 17.
Dengue virus (DENV) is a human threat of increasing importance. Although a tetravalent vaccine has been recently approved, owing to limited efficacy there is still an urgent need for antiviral drugs to prevent or treat DENV infections. Traditionally, antiviral drug discovery has focused on molecules targeting viral factors. However, thus far the identification of direct-acting antiviral drugs with potent DENV pan-serotypic activity has been problematic. An alternative are host-targeting antiviral drugs that hold great promise for broad-spectrum activity. In this review, we summarize cellular factors and pathways required by DENV for efficient replication and in principle suitable for antiviral therapy, including host-directed inhibitors that have even been advanced into clinical trials.
登革病毒(DENV)对人类的威胁日益严重。尽管最近一种四价疫苗已获批准,但由于疗效有限,仍迫切需要抗病毒药物来预防或治疗登革病毒感染。传统上,抗病毒药物的研发主要集中在针对病毒因子的分子上。然而,迄今为止,鉴定具有强大登革病毒泛血清型活性的直接作用抗病毒药物一直存在问题。另一种选择是靶向宿主的抗病毒药物,这类药物具有实现广谱活性的巨大潜力。在本综述中,我们总结了登革病毒高效复制所需的细胞因子和途径,这些在原则上适用于抗病毒治疗,包括甚至已进入临床试验阶段的宿主导向性抑制剂。