Steel Ryan Wj, Kappe Stefan Hi, Sack Brandon K
Center for Infectious Disease Research, Formerly Seattle Biomedical Research Institute, 307 Westlake Avenue North, Suite 500, Seattle, WA 98109, USA.
Future Microbiol. 2016 Dec;11(12):1563-1579. doi: 10.2217/fmb-2016-0077. Epub 2016 Nov 18.
Malaria remains a significant public health burden with 214 million new infections and over 400,000 deaths in 2015. Elucidating relevant Plasmodium parasite biology can lead to the identification of novel ways to control and ultimately eliminate the parasite within geographic areas. Particularly, the development of an effective vaccine that targets the clinically silent pre-erythrocytic stages of infection would significantly augment existing malaria elimination tools by preventing both the onset of blood-stage infection/disease as well as spread of the parasite through mosquito transmission. In this Perspective, we discuss the role of small animal models in pre-erythrocytic stage vaccine development, highlighting how human liver-chimeric and human immune system mice are emerging as valuable components of these efforts.
疟疾仍然是一项重大的公共卫生负担,2015年有2.14亿新感染病例,死亡人数超过40万。阐明疟原虫相关生物学特性有助于找到控制并最终在特定地理区域内消灭该寄生虫的新方法。特别是,开发一种针对临床上无症状的感染前期的有效疫苗,将通过预防血期感染/疾病的发生以及寄生虫通过蚊子传播,显著增强现有的疟疾消除工具。在本综述中,我们讨论了小动物模型在感染前期疫苗开发中的作用,强调了人肝嵌合小鼠和人免疫系统小鼠如何成为这些努力中有价值的组成部分。