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Host iron status and iron supplementation mediate susceptibility to erythrocytic stage Plasmodium falciparum

机译:宿主铁状态和铁补充介导对红细胞阶段恶性疟原虫的敏感性

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摘要

Iron deficiency and malaria have similar global distributions, and frequently co-exist in pregnant women and young children. Where both conditions are prevalent, iron supplementation is complicated by observations that iron deficiency anaemia protects against falciparum malaria, and that iron supplements increase susceptibility to clinically significant malaria, but the mechanisms remain obscure. Here, using an in vitro parasite culture system with erythrocytes from iron-deficient and replete human donors, we demonstrate that Plasmodium falciparum infects iron-deficient erythrocytes less efficiently. In addition, owing to merozoite preference for young erythrocytes, iron supplementation of iron-deficient individuals reverses the protective effects of iron deficiency. Our results provide experimental validation of field observations reporting protective effects of iron deficiency and harmful effects of iron administration on human malaria susceptibility. Because recovery from anaemia requires transient reticulocytosis, our findings imply that in malarious regions iron supplementation should be accompanied by effective measures to prevent falciparum malaria.
机译:缺铁和疟疾在全球分布相似,在孕妇和幼儿中经常并存。在两种情况都普遍存在的情况下,铁的补充由于观察到缺铁性贫血可预防恶性疟疾而变得复杂,铁的补充增加了对临床上显着的疟疾的易感性,但机制仍不清楚。在这里,使用体外寄生虫培养系统与缺铁和充足人类供体的红细胞,我们证明恶性疟原虫感染铁缺乏红细胞的效率较低。此外,由于裂殖子对幼年红细胞的偏好,缺铁个体的补铁会逆转缺铁的保护作用。我们的结果提供了实地观察的实验验证,报告了铁缺乏的保护作用和铁施用对人类疟疾易感性的有害影响。因为从贫血中恢复需要短暂的网状细胞增多,所以我们的发现表明在疟疾流行地区,应补充铁剂并采取有效措施预防恶性疟疾。

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