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疟原虫自然感染的动力学。

The dynamics of natural Plasmodium falciparum infections.

机构信息

Swiss Tropical and Public Health Institute, Basel, Switzerland.

出版信息

PLoS One. 2012;7(9):e45542. doi: 10.1371/journal.pone.0045542. Epub 2012 Sep 18.

Abstract

BACKGROUND

Natural immunity to Plasmodium falciparum has been widely studied, but its effects on parasite dynamics are poorly understood. Acquisition and clearance rates of untreated infections are key elements of the dynamics of malaria, but estimating these parameters is challenging because of frequent super-infection and imperfect detectability of parasites. Consequently, information on effects of host immune status or age on infection dynamics is fragmentary.

METHODS

An age-stratified cohort of 347 individuals from Northern Ghana was sampled six times at 2 month intervals. High-throughput capillary electrophoresis was used to genotype the msp-2 locus of all P. falciparum infections detected by PCR. Force of infection (FOI) and duration were estimated for each age group using an immigration-death model that allows for imperfect detection of circulating parasites.

RESULTS

Allowing for imperfect detection substantially increased estimates of FOI and duration. Effects of naturally acquired immunity on the FOI and duration would be reflected in age dependence in these indices, but in our cohort data FOI tended to increase with age in children. Persistence of individual parasite clones was characteristic of all age-groups. Duration peaked in 5-9 year old children (average duration 319 days, 95% confidence interval 318;320).

CONCLUSIONS

The main age-dependence is on parasite densities, with only small age-variations in the FOI and persistence of infections. This supports the hypothesis that acquired immunity controls transmission mainly by limiting blood-stage parasite densities rather than changing rates of acquisition or clearance of infections.

摘要

背景

人们广泛研究了疟原虫自然免疫,但对其对寄生虫动力学的影响知之甚少。未治疗感染的获得和清除率是疟疾动力学的关键要素,但由于频繁的超级感染和寄生虫检测的不完美性,估计这些参数具有挑战性。因此,关于宿主免疫状态或年龄对感染动态的影响的信息是零碎的。

方法

来自加纳北部的 347 名年龄分层的个体在 2 个月的间隔内进行了六次采样。使用高通量毛细管电泳对通过 PCR 检测到的所有疟原虫感染的 msp-2 基因座进行基因分型。使用移民-死亡模型估计每个年龄组的感染率(FOI)和持续时间,该模型允许循环寄生虫的检测不完美。

结果

允许检测不完美性大大增加了 FOI 和持续时间的估计值。自然获得的免疫力对 FOI 和持续时间的影响将反映在这些指标的年龄依赖性中,但在我们的队列数据中,FOI 在儿童中随着年龄的增长而增加。个体寄生虫克隆的持久性是所有年龄组的特征。持续时间在 5-9 岁的儿童中达到峰值(平均持续时间为 319 天,95%置信区间为 318;320)。

结论

主要的年龄依赖性是寄生虫密度,感染的 FOI 和持久性只有很小的年龄变化。这支持了获得的免疫力主要通过限制血液阶段寄生虫密度而不是改变感染的获得或清除率来控制传播的假设。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d749/3445515/cc793954036b/pone.0045542.g001.jpg

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