Palacpac Nirianne Marie Q, Horii Toshihiro
Department of Malaria Vaccine Development, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.
F1000Res. 2020 Apr 27;9. doi: 10.12688/f1000research.22143.1. eCollection 2020.
Much of the gain in malaria control, in terms of regional achievements in restricting geographical spread and reducing malaria cases and deaths, can be attributed to large-scale deployment of antimalarial drugs, insecticide-treated bed nets, and early diagnostics. However, despite impressive progress, control efforts have stalled because of logistics, unsustainable delivery, or short-term effectiveness of existing interventions or a combination of these reasons. A highly efficacious malaria vaccine as an additional tool would go a long way, but success in the development of this important intervention remains elusive. Moreover, most of the vaccine candidate antigens that were investigated in early-stage clinical trials, selected partly because of their immunogenicity and abundance during natural malaria infection, were polymorphic or structurally complex or both. Likewise, we have a limited understanding of immune mechanisms that confer protection. We reflect on some considerable technological and scientific progress that has been achieved and the lessons learned.
就疟疾控制在限制地理传播以及减少疟疾病例和死亡方面的区域成就而言,很大程度上可归因于抗疟药物、经杀虫剂处理的蚊帐和早期诊断方法的大规模部署。然而,尽管取得了令人瞩目的进展,但由于后勤问题、现有干预措施的不可持续交付或短期有效性,或这些原因的综合作用,控制工作陷入了停滞。一种高效的疟疾疫苗作为一种额外的工具将大有帮助,但这种重要干预措施的研发成功仍然难以实现。此外,在早期临床试验中研究的大多数候选疫苗抗原,部分是因为它们在自然疟疾感染期间的免疫原性和丰度而被选择的,这些抗原具有多态性或结构复杂,或两者兼而有之。同样,我们对赋予保护作用的免疫机制了解有限。我们回顾了已经取得的一些重大技术和科学进展以及吸取的经验教训。