Seattle Biomedical Research Institute and Department of Global Health, University of Washington, Seattle, Washington, USA.
Expert Rev Mol Med. 2009 Dec 16;11:e39. doi: 10.1017/S1462399409001318.
Malaria remains one of the most devastating infectious diseases that threaten humankind. Human malaria is caused by five different species of Plasmodium parasites, each transmitted by the bite of female Anopheles mosquitoes. Plasmodia are eukaryotic protozoans with more than 5000 genes and a complex life cycle that takes place in the mosquito vector and the human host. The life cycle can be divided into pre-erythrocytic stages, erythrocytic stages and mosquito stages. Malaria vaccine research and development faces formidable obstacles because many vaccine candidates will probably only be effective in a specific species at a specific stage. In addition, Plasmodium actively subverts and escapes immune responses, possibly foiling vaccine-induced immunity. Although early successful vaccinations with irradiated, live-attenuated malaria parasites suggested that a vaccine is possible, until recently, most efforts have focused on subunit vaccine approaches. Blood-stage vaccines remain a primary research focus, but real progress is evident in the development of a partially efficacious recombinant pre-erythrocytic subunit vaccine and a live-attenuated sporozoite vaccine. It is unlikely that partially effective vaccines will eliminate malaria; however, they might prove useful in combination with existing control strategies. Elimination of malaria will probably ultimately depend on the development of highly effective vaccines.
疟疾仍然是威胁人类的最具破坏性的传染病之一。人类疟疾是由五种不同的疟原虫寄生虫引起的,每种寄生虫都是由雌性疟蚊叮咬传播的。疟原虫是具有 5000 多个基因的真核原生动物,其生命周期复杂,在蚊子媒介和人类宿主中进行。生命周期可分为红细胞前期、红细胞期和蚊媒期。疟疾疫苗的研究和开发面临着巨大的障碍,因为许多候选疫苗可能只在特定物种的特定阶段有效。此外,疟原虫积极地颠覆和逃避免疫反应,可能会破坏疫苗诱导的免疫。尽管早期用辐照、减毒活疟疾寄生虫进行成功的疫苗接种表明疫苗是可能的,但直到最近,大多数努力都集中在亚单位疫苗方法上。血期疫苗仍然是主要的研究重点,但在开发部分有效的重组红细胞前期亚单位疫苗和减毒活孢子疫苗方面已经取得了明显进展。部分有效的疫苗不太可能消除疟疾;然而,它们可能与现有的控制策略结合使用证明是有用的。消除疟疾可能最终取决于高度有效的疫苗的开发。