a UPMC Faculte de Medecine - INSERM U1135, CNRS ERL 8255, Centre d'Immunologie et des Maladies Infectieuses (CIMI-Paris) , Paris, Île-de-France France.
b Assistance Publique - Hopitaux de Paris - Hôpitaux Universitaires Paris-Est - Site Saint-Antoine , Paris, Île-de-France France.
Expert Opin Drug Discov. 2018 Feb;13(2):131-140. doi: 10.1080/17460441.2018.1410136. Epub 2017 Nov 28.
Efforts on malaria drug discovery are expected to increase in the coming years to achieve malaria eradication. Owing to the increasing number of new potential candidates together with the actual limitations of the primate models, humanized mouse models infected with human Plasmodium spp. (HmHP) now appear as an alternative to the primate model. Areas covered: The authors review the progress obtained in the HmHP in the last two decades, with a special emphasis of their input on the drug discovery pathway. The authors discuss the methodologies and strategies used in these models to obtain an accurate assessment of the compound activity and a reliable prediction of the human efficacious regimen. Expert opinion: Research efforts have led us to an era in which HmHP can successfully be infected with P. falciparum, P vivax and P. ovale. Furthermore, it is now a reality that the complete human cycle of P. falciparum can be obtained in HmHP. The HmHP has shown a real input mainly in the preclinical evaluation of new compounds against the erythrocytic stages of P. falciparum. However, further technical improvements are needed before HmHP may replace the primate model.
未来几年,预计将加大疟疾药物研发力度,以实现疟疾消除。由于新的潜在候选药物数量不断增加,以及灵长类动物模型的实际局限性,感染人类疟原虫的人源化小鼠模型(HmHP)现在似乎成为灵长类动物模型的替代品。
作者回顾了过去二十年中在 HmHP 中取得的进展,特别强调了它们在药物发现途径中的投入。作者讨论了这些模型中使用的方法和策略,以对化合物活性进行准确评估,并对人类有效方案进行可靠预测。
研究工作使我们进入了一个时代,在这个时代,HmHP 可以成功感染恶性疟原虫、间日疟原虫和卵形疟原虫。此外,现在已经可以在 HmHP 中获得恶性疟原虫的完整人类生命周期。HmHP 主要在新化合物对抗恶性疟原虫红细胞阶段的临床前评估中发挥了实际作用。然而,在 HmHP 可能取代灵长类动物模型之前,还需要进一步的技术改进。