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促红细胞生成素诱导的网织红细胞增多对血液期疟疾病程及转归的调节作用

Modulation of the course and outcome of blood-stage malaria by erythropoietin-induced reticulocytosis.

作者信息

Chang Kai-Hsin, Tam Mifong, Stevenson Mary M

机构信息

Institute of Parasitology, McGill University, Macdonald Campus, Ste. Anne de Bellevue, Montreal General Hospital Research Institute, 1650 Cedar Avenue, Montreal, Quebec H3G 1A4, Canada.

出版信息

J Infect Dis. 2004 Feb 15;189(4):735-43. doi: 10.1086/381458. Epub 2004 Jan 30.

Abstract

Severe anemia is a major life-threatening complication of malaria. The roles of erythropoietin (Epo) and erythropoiesis during blood-stage malaria were investigated. By treating Plasmodium chabaudi AS-infected C57BL/6 (B6) mice, which are resistant to malaria, with polyclonal anti-human Epo neutralizing antibody, we demonstrated that Epo-induced reticulocytosis was important for alleviating malarial anemia and for host survival. By inducing erythropoiesis in A/J mice, which are susceptible to malaria, and in B6 mice at various periods during infection, by use of exogenous recombinant murine Epo, untimely onset of reticulocytosis was shown to augment multiplication of parasites and result in lethal infection. However, timely inducement of reticulocytosis with Epo treatment alleviated malarial anemia and increased survival. Our data reveal the important role of Epo-induced reticulocytosis in modulating the course and outcome of blood-stage malaria. However, the mechanisms underlying the increased mortality associated with untimely treatment with Epo and the increased protection associated with timely treatment with Epo remain to be investigated.

摘要

严重贫血是疟疾的一种主要的危及生命的并发症。我们研究了促红细胞生成素(Epo)和红细胞生成在血液期疟疾中的作用。通过用多克隆抗人Epo中和抗体处理感染了恰氏疟原虫AS的C57BL/6(B6)小鼠(该小鼠对疟疾具有抗性),我们证明Epo诱导的网织红细胞增多对于减轻疟疾贫血和宿主存活很重要。通过使用外源性重组鼠Epo在易患疟疾的A/J小鼠以及感染期间不同阶段的B6小鼠中诱导红细胞生成,结果显示网织红细胞增多的过早发生会增加寄生虫的增殖并导致致命感染。然而,用Epo治疗及时诱导网织红细胞增多可减轻疟疾贫血并提高存活率。我们的数据揭示了Epo诱导的网织红细胞增多在调节血液期疟疾的病程和结局中的重要作用。然而,与Epo治疗不及时相关的死亡率增加以及与Epo治疗及时相关的保护作用增加的潜在机制仍有待研究。

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