Queensland Institute for Medical Research.
J Infect Dis. 2013 Nov 15;208(10):1688-94. doi: 10.1093/infdis/jit394. Epub 2013 Aug 1.
Major impediments to development of vaccines and drugs for Plasmodium vivax malaria are the inability to culture this species and the extreme difficulty in undertaking clinical research by experimental infection.
A parasite bank was collected from a 49-year-old woman with P. vivax infection, characterized, and used in an experimental infection study.
The donor made a full recovery from malaria after collection of a parasite bank, which tested negative for agents screened for in blood donations. DNA sequence analysis of the isolate indicated that it was clonal. Two subjects inoculated with the isolate became polymerase chain reaction positive on days 8 and 9, with onset of symptoms and positive blood smears on day 14, when they were treated with artemether-lumefantrine, with rapid clinical and parasitologic response. Transcripts of the parasite gene pvs25 that is expressed in gametocytes, the life cycle stage infectious to mosquitoes, were first detected on days 11 and 12.
This experimental system results in in vivo parasite growth, probably infectious to mosquitoes. It offers the opportunity to undertake studies previously impossible in P. vivax that will facilitate a better understanding of the pathology of vivax malaria and development of antimalarial drugs and vaccines. Trial Registration. ANZCTR: 12612001096842.
阻碍间日疟原虫疫苗和药物研发的主要障碍是无法培养这种寄生虫,以及通过实验性感染进行临床研究极其困难。
从一名患有间日疟原虫感染的 49 岁女性中采集寄生虫库,对其进行特征描述,并用于实验性感染研究。
在采集寄生虫库后,供体从疟疾中完全康复,寄生虫库经血液捐献筛查的试剂检测均为阴性。分离株的 DNA 序列分析表明其为克隆。两名接种者在第 8 天和第 9 天聚合酶链反应呈阳性,第 14 天出现症状和阳性血涂片,此时他们用青蒿琥酯-甲氟喹治疗,迅速出现临床和寄生虫学反应。寄生虫基因 pvs25 的转录本在配子体中表达,配子体是对蚊子具有感染性的生命周期阶段,于第 11 天和第 12 天首次检测到。
该实验系统导致体内寄生虫生长,可能对蚊子具有传染性。它为以前在间日疟原虫中无法进行的研究提供了机会,将有助于更好地理解间日疟原虫的病理学以及抗疟药物和疫苗的开发。
ANZCTR:12612001096842。