Department of Pediatrics, University of Texas Medical Branch, Galveston, TX 77555, USA; Sealy Center for Vaccine Development, University of Texas Medical Branch, Galveston, TX 77555, USA; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Department of Pediatrics, University of Texas Medical Branch, Galveston, TX 77555, USA.
Antiviral Res. 2018 Jun;154:104-109. doi: 10.1016/j.antiviral.2018.04.012. Epub 2018 Apr 14.
Dengue is a mosquito-borne disease of global public health importance caused by four genetically and serologically related viruses (DENV-1 to DENV-4). Efforts to develop effective vaccines and therapeutics for dengue have been slowed by the paucity of preclinical models that mimic human disease. DENV-2 models in interferon receptor deficient AG129 mice were an important advance but only allowed testing against a single DENV serotype. We have developed complementary AG129 mouse models of severe disseminated dengue infection using strains of the other three DENV serotypes. Here we used the adenosine nucleoside inhibitor NITD-008 to show that these models provide the ability to perform comparative preclinical efficacy testing of candidate antivirals in vivo against the full-spectrum of DENV serotypes. Although NITD-008 was effective in modulating disease caused by all DENV serotypes, the variability in protection among DENV serotypes was greater than expected from differences in activity in in vitro testing studies emphasizing the need to undertake spectrum of activity testing to help in prioritization of candidate compounds for further development.
登革热是一种由 4 种基因和血清相关的病毒(DENV-1 至 DENV-4)引起的具有全球公共卫生重要性的蚊媒疾病。由于缺乏模拟人类疾病的临床前模型,因此开发有效的登革热疫苗和治疗方法的工作进展缓慢。干扰素受体缺陷型 AG129 小鼠中的 DENV-2 模型是一项重要进展,但仅允许针对单一 DENV 血清型进行测试。我们使用其他三种 DENV 血清型的菌株开发了严重播散性登革热感染的互补 AG129 小鼠模型。在这里,我们使用腺苷核苷抑制剂 NITD-008 表明,这些模型提供了在体内针对 DENV 血清型全谱对候选抗病毒药物进行比较临床前疗效测试的能力。尽管 NITD-008 对所有 DENV 血清型引起的疾病均有效,但 DENV 血清型之间的保护差异大于体外测试研究中活性差异所预期的,这强调了需要进行活性谱测试以帮助确定候选化合物的优先级,以便进一步开发。