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一种评估干预措施疗效的间日疟原虫实验性人体感染模型。

A Plasmodium vivax experimental human infection model for evaluating efficacy of interventions.

机构信息

QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.

Department of Medical Microbiology, Radboud University Medical Centre, Nijmegen, Netherlands.

出版信息

J Clin Invest. 2020 Jun 1;130(6):2920-2927. doi: 10.1172/JCI134923.

Abstract

BACKGROUNDInterventions that interrupt Plasmodium vivax transmission or eliminate dormant P. vivax liver-stage parasites will be essential for malaria elimination. Development of these interventions has been hindered by the lack of P. vivax in vitro culture and could be accelerated by a safe and reproducible clinical model in malaria-naive individuals.METHODSHealthy, malaria-naive adults were enrolled in 2 studies to assess the safety, infectivity, and transmissibility of a new P. vivax isolate. Participants (Study 1, n = 2; Study 2, n = 24) were inoculated with P. vivax-infected red blood cells to initiate infection, and were treated with artemether-lumefantrine (Study 1) or chloroquine (Study 2). Primary endpoints were safety and infectivity of the new isolate. In Study 2, transmission to mosquitoes was also evaluated using mosquito feeding assays, and sporozoite viability was assessed using in vitro cultured hepatocytes.RESULTSParasitemia and gametocytemia developed in all participants and was cleared by antimalarial treatment. Adverse events were mostly mild or moderate and none were serious. Sixty-nine percent of participants (11/16) were infectious to Anopheles mosquitoes at peak gametocytemia. Mosquito infection rates reached 97% following membrane feeding with gametocyte-enriched blood, and sporozoites developed into liver-stage schizonts in culture.CONCLUSIONWe have demonstrated the safe, reproducible, and efficient transmission of P. vivax gametocytes from humans to mosquitoes, and have established an experimental model that will accelerate the development of interventions targeting multiple stages of the P. vivax life cycle.TRIAL REGISTRATIONACTRN12614000930684 and ACTRN12616000174482.FUNDING(Australian) National Health and Medical Research Council Program Grant 1132975 (Study 1). Bill and Melinda Gates Foundation (OPP1111147) (Study 2).

摘要

背景

阻断间日疟原虫传播或消除休眠的间日疟原虫肝脏期寄生虫将是消除疟疾的关键。由于缺乏间日疟原虫的体外培养,这些干预措施的发展受到了阻碍,而在无疟疾个体中建立一种安全且可重复的临床模型可能会加速这一进程。

方法

在两项研究中,健康的、无疟疾史的成年人被招募来评估一种新的间日疟原虫分离株的安全性、感染性和传染性。参与者(研究 1,n=2;研究 2,n=24)接受感染的间日疟原虫红细胞接种以启动感染,并接受青蒿琥酯-咯萘啶(研究 1)或氯喹(研究 2)治疗。主要终点是新分离株的安全性和感染性。在研究 2 中,还使用蚊子喂食试验评估了向蚊子的传播情况,并使用体外培养的肝细胞评估了孢子体活力。

结果

所有参与者均出现疟原虫血症和配子体血症,并通过抗疟治疗清除。不良事件大多为轻度或中度,无严重不良事件。在峰值配子体血症时,有 69%的参与者(11/16)对疟蚊具有感染性。用富含配子体的血液进行膜喂食后,蚊子感染率达到 97%,孢子体在培养中发育成肝脏期裂殖体。

结论

我们已经证明了从人类向蚊子安全、可重复和高效地传播间日疟原虫配子体,并建立了一个实验模型,该模型将加速针对间日疟原虫生命周期多个阶段的干预措施的发展。

试验注册

ACTRN12614000930684 和 ACTRN12616000174482。

资金(澳大利亚)国家健康与医学研究理事会项目拨款 1132975(研究 1)。比尔和梅琳达·盖茨基金会(OPP1111147)(研究 2)。

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