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比较无并发症和严重儿童恶性疟原虫疟疾中的寄生虫隔离。

Comparison of parasite sequestration in uncomplicated and severe childhood Plasmodium falciparum malaria.

机构信息

Department of Immunology and Infection, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT, UK.

出版信息

J Infect. 2013 Sep;67(3):220-30. doi: 10.1016/j.jinf.2013.04.013. Epub 2013 Apr 23.

Abstract

OBJECTIVES

To determine whether sequestration of parasitized red blood cells differs between children with uncomplicated and severe Plasmodium falciparum malaria.

METHODS

We quantified circulating-, total- and sequestered-parasite biomass, using a mathematical model based on plasma concentration of P. falciparum histidine rich protein 2, in Gambian children with severe (n = 127) and uncomplicated (n = 169) malaria.

RESULTS

Circulating- and total-, but not sequestered-, parasite biomass estimates were significantly greater in children with severe malaria than in those with uncomplicated malaria. Sequestered biomass estimates in children with hyperlactataemia or prostration were similar to those in uncomplicated malaria, whereas sequestered biomass was higher in patients with severe anaemia, and showed a trend to higher values in cerebral malaria and fatal cases. Blood lactate concentration correlated with circulating- and total-, but not sequestered parasite biomass. These findings were robust after controlling for age, prior antimalarial treatment and clonality of infection, and over a realistic range of variation in model parameters.

CONCLUSION

Extensive sequestration is not a uniform requirement for severe paediatric malaria. The pathophysiology of hyperlactataemia and prostration appears to be unrelated to sequestered parasite biomass. Different mechanisms may underlie different severe malaria syndromes, and different therapeutic strategies may be required to improve survival.

摘要

目的

确定寄生虫感染的红细胞在无并发症和严重恶性疟原虫疟疾儿童之间是否存在差异。

方法

我们使用基于恶性疟原虫游离组氨酸丰富蛋白 2 血浆浓度的数学模型,定量检测冈比亚儿童无并发症(n=169)和严重疟疾(n=127)的循环、总和寄生生物质。

结果

严重疟疾儿童的循环和总寄生虫生物量估计值,但不是寄生虫滞留量,均明显高于无并发症疟疾儿童。乳酸酸中毒或虚脱的儿童的寄生虫滞留量与无并发症疟疾相似,而严重贫血的儿童的寄生虫滞留量较高,并且在脑型疟疾和致命病例中,寄生虫滞留量有更高的趋势。血乳酸浓度与循环和总寄生虫生物量相关,但与寄生虫滞留量无关。这些发现经过年龄、先前抗疟治疗和感染的克隆性控制以及模型参数的实际变化范围的调整后仍然成立。

结论

广泛的滞留并不是严重儿童疟疾的普遍要求。乳酸酸中毒和虚脱的病理生理学似乎与寄生虫滞留量无关。不同的严重疟疾综合征可能有不同的发病机制,可能需要不同的治疗策略来提高生存率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc3f/3744804/50411d652327/gr1.jpg

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