Interventions & Clinical Trials Department, Ifakara Health Institute, P.O. Box 74, Bagamoyo, Tanzania.
Nelson Mandela African Institution of Science and Technology, Tengeru, P. O. Box 447, Arusha, Tanzania.
Malar J. 2022 Jun 2;21(1):159. doi: 10.1186/s12936-022-04173-y.
Malaria control relies heavily on the use of anti-malarial drugs and insecticides against malaria parasites and mosquito vectors. Drug and insecticide resistance threatens the effectiveness of conventional malarial interventions; alternative control approaches are, therefore, needed. The development of malaria transmission-blocking vaccines that target the sexual stages in humans or mosquito vectors is among new approaches being pursued. Here, the immunological mechanisms underlying malaria transmission blocking, status of Pfs25-based vaccines are viewed, as well as approaches and capacity for first in-human evaluation of a transmission-blocking candidate vaccine Pfs25-IMX313/Matrix-M administered to semi-immune healthy individuals in endemic settings. It is concluded that institutions in low and middle income settings should be supported to conduct first-in human vaccine trials in order to stimulate innovative research and reduce the overdependence on developed countries for research and local interventions against many diseases of public health importance.
疟疾控制主要依赖于使用抗疟药物和杀虫剂来对抗疟原虫和蚊子媒介。药物和杀虫剂耐药性威胁着常规疟疾干预措施的有效性;因此,需要替代控制方法。正在探索的新方法之一是开发针对人类或蚊子媒介有性阶段的疟疾传播阻断疫苗。本文综述了疟疾传播阻断的免疫机制、基于 Pf s25 的疫苗的现状,以及在流行地区对半免疫健康个体接种Pf s25-IMX313/Matrix-M 候选疫苗进行首次人体试验的方法和能力。结论是,应支持中低收入国家的机构开展首次人体疫苗试验,以激发创新性研究,减少对发达国家在许多重要公共卫生疾病的研究和本地干预的过度依赖。