Special Pathogens Programme, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada; Department of Medical Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada.
Special Pathogens Programme, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
Clin Microbiol Infect. 2019 Apr;21S:e17-e27. doi: 10.1111/1469-0691.12630. Epub 2015 Jun 22.
Viral haemorrhagic fever can be caused by one of a diverse group of viruses that come from four different families of RNA viruses. Disease severity can vary from mild self-limiting febrile illness to severe disease characterized by high fever, high-level viraemia, increased vascular permeability that can progress to shock, multi-organ failure and death. Despite the urgent need, effective treatments and preventative vaccines are currently lacking for the majority of these viruses. A number of factors preclude the effective study of these diseases in humans including the high virulence of the agents involved, the sporadic nature of outbreaks of these viruses, which are typically in geographically isolated areas with underserviced diagnostic capabilities, and the requirements for high level bio-containment. As a result, animal models that accurately mimic human disease are essential for advancing our understanding of the pathogenesis of viral haemorrhagic fevers. Moreover, animal models for viral haemorrhagic fevers are necessary to test vaccines and therapeutic intervention strategies. Here, we present an overview of the animal models that have been established for each of the haemorrhagic fever viruses and identify which aspects of human disease are modelled. Furthermore, we discuss how experimental design considerations, such as choice of species and virus strain as well as route and dose of inoculation, have an influence on animal model development. We also bring attention to some of the pitfalls that need to be avoided when extrapolating results from animal models.
病毒性出血热可由来自四种不同 RNA 病毒家族的多种病毒引起。疾病的严重程度从轻微的自限性发热疾病到以高热、高水平病毒血症、增加的血管通透性为特征的严重疾病不等,这些都可能进展为休克、多器官衰竭和死亡。尽管有迫切的需求,但目前大多数这些病毒仍然缺乏有效的治疗方法和预防疫苗。一些因素妨碍了对这些疾病在人类中的有效研究,包括相关病原体的高毒性、这些病毒爆发的零星性质,这些病毒通常发生在地理上孤立的地区,诊断能力不足,并且需要高水平的生物控制。因此,能够准确模拟人类疾病的动物模型对于深入了解病毒性出血热的发病机制至关重要。此外,病毒性出血热的动物模型对于测试疫苗和治疗干预策略也是必要的。在这里,我们概述了为每种出血热病毒建立的动物模型,并确定了哪些方面的人类疾病得到了模拟。此外,我们还讨论了实验设计考虑因素(如物种和病毒株的选择以及接种途径和剂量)如何影响动物模型的发展。我们还提请注意在从动物模型推断结果时需要避免的一些陷阱。