Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Avenue Prof. Egas Moniz, 1649-028 Lisboa, Portugal.
EMBO Rep. 2011 Dec 1;12(12):1233-42. doi: 10.1038/embor.2011.213.
After the bite of a malaria-infected mosquito, the Plasmodium sporozoite infects liver cells and produces thousands of merozoites, which then infect red blood cells, causing malaria. In malaria-endemic areas, several hundred infected mosquitoes can bite an individual each year, increasing the risk of superinfection. However, in infants that are yet to acquire immunity, superinfections are infrequent. We have recently shown that blood-stage parasitaemia, above a minimum threshold, impairs the growth of a subsequent sporozoite infection of liver cells. Blood-stage parasites stimulate the production of the host iron-regulatory factor hepcidin, which redistributes iron away from hepatocytes, reducing the development of the iron-dependent liver stage. This could explain why Plasmodium superinfection is not often found in young nonimmune children. Here, we discuss the impact that such protection from superinfection might have in epidemiological settings or in programmes for controlling malaria, as well as how the induction of hepcidin and redistribution of iron might influence anaemia and the outcome of non-Plasmodium co-infections.
被感染疟疾的蚊子叮咬后,疟原虫子孢子感染肝细胞并产生数千个裂殖子,裂殖子随后感染红细胞,导致疟疾。在疟疾流行地区,每年可能有数百只受感染的蚊子叮咬一个人,增加了再次感染的风险。然而,在尚未获得免疫力的婴儿中,再次感染并不常见。我们最近表明,血液阶段寄生虫血症超过最低阈值会损害随后感染肝细胞的子孢子感染的生长。血液阶段寄生虫刺激宿主铁调节因子铁调素的产生,将铁从肝细胞重新分配,从而减少铁依赖性肝期的发育。这可以解释为什么年轻的非免疫儿童中通常不会发现疟原虫再次感染。在这里,我们讨论了这种免受再次感染的保护可能对流行病学环境或疟疾控制计划产生的影响,以及铁调素的诱导和铁的重新分配如何影响贫血和非疟原虫合并感染的结果。