Jiménez-Díaz María-Belén, Möhrle Jörg J, Angulo-Barturen Iñigo, Demarta-Gatsi Claudia
The Art of Discovery, 48160 Derio, Basque Country, Spain.
Medicines for Malaria Venture, 1215 Geneva, Switzerland.
Microorganisms. 2023 Aug 31;11(9):2209. doi: 10.3390/microorganisms11092209.
In addition to vector control, long-lasting insecticidal nets and case management, the prevention of infection through vaccination and/or chemoprevention are playing an increasing role in the drive to eradicate malaria. These preventative approaches represent opportunities for improvement: new drugs may be discovered that target the early infectious stages of the parasite in the liver (rather than the symptomatic, abundant blood stage), and new, exciting vaccination technologies have recently been validated (using mRNA or novel adjuvants). Exploiting these possibilities requires the availability of humanized mouse models that support infection yet avoid the hazardous use of infectious mosquitoes. Here, we show that commercially available sporozoites and FRG mice carrying human hepatocytes and red blood cells faithfully recapitulate the early human malaria disease process, presenting an opportunity to use this model for the evaluation of prophylactic treatments with a novel mode of action.
除了病媒控制、长效驱虫蚊帐和病例管理外,通过疫苗接种和/或化学预防来预防感染在根除疟疾的努力中发挥着越来越重要的作用。这些预防方法存在改进的机会:可能会发现针对寄生虫在肝脏中早期感染阶段(而非有症状的、数量众多的血液阶段)的新药,并且最近新的、令人兴奋的疫苗技术已经得到验证(使用信使核糖核酸或新型佐剂)。利用这些可能性需要有支持感染但避免使用感染性蚊子这种危险做法的人源化小鼠模型。在此,我们表明,市售的子孢子以及携带人类肝细胞和红细胞的FRG小鼠忠实地再现了早期人类疟疾疾病过程,为使用该模型评估具有新型作用方式的预防性治疗提供了机会。