Small Animal Models for Evaluating Filovirus Countermeasures

被引:15
|
作者
Banadyga, Logan [1 ,2 ]
Wong, Gary [1 ,2 ,3 ]
Qiu, Xiangguo [1 ,2 ]
机构
[1] Publ Hlth Agcy Canada, Special Pathogens Program, Natl Microbiol Lab, 1015 Arlington St, Winnipeg, MB R3E 3R2, Canada
[2] Univ Manitoba, Dept Med Microbiol & Infect Dis, 745 Bannatyne St, Winnipeg, MB R3E 0J9, Canada
[3] Third Peoples Hosp, Shenzhen Key Lab Pathogen & Immun, Guangdong Key Lab Diag & Treatment Emerging Infec, 29 Bulan Rd, Shenzhen 518000, Peoples R China
来源
ACS INFECTIOUS DISEASES | 2018年 / 4卷 / 05期
基金
中国国家自然科学基金; 加拿大健康研究院;
关键词
filovirus; Ebola virus; Marburg virus; countermeasure development; vaccine; therapeutic; animal models; rodent models; ferrets; EBOLA-VIRUS DISEASE; VERVET MONKEY DISEASE; SYRIAN GOLDEN-HAMSTER; HUMANIZED MOUSE MODEL; MUSTELA-PUTORIUS-FURO; GUINEA-PIGS; IN-VIVO; HEMORRHAGIC-FEVER; ADJUVANT ACTIVITY; IMMUNE-RESPONSES;
D O I
10.1021/acsinfecdis.7b00266
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The development of novel therapeutics and vaccines to treat or prevent disease caused by filoviruses, such as Ebola and Marburg viruses, depends on the availability of animal models that faithfully recapitulate clinical hallmarks of disease as it is observed in humans. In particular, small animal models (such as mice and guinea pigs) are historically and frequently used for the primary evaluation of antiviral countermeasures, prior to testing in nonhuman primates, which represent the gold-standard filovirus animal model. In the past several years, however, the filovirus field has witnessed the continued refinement of the mouse and guinea pig models of disease, as well as the introduction of the hamster and ferret models. We now have small animal models for most human-pathogenic filoviruses, many of which are susceptible to wild type virus and demonstrate key features of disease, including robust virus replication, coagulopathy, and immune system dysfunction. Although none of these small animal model systems perfectly recapitulates Ebola virus disease or Marburg virus disease on its own, collectively they offer a nearly complete set of tools in which to carry out the preclinical development of novel antiviral drugs.
引用
收藏
页码:673 / 685
页数:25
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