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在一个全流行地区人群中,恶性疟原虫血期寄生虫增长率随年龄下降。

Decreased growth rate of P. falciparum blood stage parasitemia with age in a holoendemic population.

机构信息

Centre for Vascular Research, University of New South Wales, Sydney, New South Wales, Australia.

出版信息

J Infect Dis. 2014 Apr 1;209(7):1136-43. doi: 10.1093/infdis/jit613. Epub 2013 Nov 21.

Abstract

In malaria holoendemic settings, decreased parasitemia and clinical disease is associated with age and cumulative exposure. The relative contribution of acquired immunity against various stages of the parasite life cycle is not well understood. In particular, it is not known whether changes in infection dynamics can be best explained by decreasing rates of infection, or by decreased growth rates of parasites in blood. Here, we analyze the dynamics of Plasmodium falciparum infection after treatment in a cohort of 197 healthy study participants of different ages. We use both polymerase chain reaction (PCR) and microscopy detection of parasitemia in order to understand parasite growth rates and infection rates over time. The more sensitive PCR assay detects parasites earlier than microscopy, and demonstrates a higher overall prevalence of infection than microscopy alone. The delay between PCR and microscopy detection is significantly longer in adults compared with children, consistent with slower parasite growth with age. We estimated the parasite multiplication rate from delay to PCR and microscopy detections of parasitemia. We find that both the delay between PCR and microscopy infection as well as the differing reinfection dynamics in different age groups are best explained by a slowing of parasite growth with age.

摘要

在疟疾全疫区环境中,寄生虫血症减少和临床疾病与年龄和累积暴露有关。针对寄生虫生命周期各个阶段获得性免疫的相对贡献尚不清楚。特别是,尚不清楚感染动态的变化是否可以通过感染率的降低,或者通过血液中寄生虫的生长率的降低来最好地解释。在这里,我们分析了在不同年龄的 197 名健康研究参与者的队列中,治疗后疟原虫感染的动态。我们使用聚合酶链反应(PCR)和寄生虫血症的显微镜检测来了解随时间推移的寄生虫生长率和感染率。更敏感的 PCR 检测比显微镜更早地检测到寄生虫,并证明比单独显微镜检测更高的总感染率。与儿童相比,PCR 和显微镜检测之间的延迟在成年人中明显更长,这与年龄相关的寄生虫生长速度较慢一致。我们从寄生虫血症的 PCR 和显微镜检测之间的延迟估计寄生虫倍增率。我们发现,PCR 和显微镜感染之间的延迟以及不同年龄组的不同再感染动态都可以通过寄生虫随年龄增长而生长速度减慢来最好地解释。

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