Molecular Biology of Malaria and Opportunistic Parasites Research Unit, Department of Parasitology, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand.
Vaccine. 2010 Apr 19;28(18):3112-7. doi: 10.1016/j.vaccine.2010.02.062. Epub 2010 Mar 1.
A number of cell surface antigens of the infective stages of malaria parasites (genus Plasmodium) have been proposed as vaccine candidates, but high levels of polymorphism at the loci encoding these antigens are problematic for vaccine effectiveness. In order to test for the effects of anti-malarial control measures (including drugs and vector control) on polymorphism at antigen-encoding loci, we analyzed sequences of four antigen-encoding loci from P. vivax and two from P. falciparum collected in 2006-2007 from two areas of Thailand: (1) the NW, where malaria cases have remained high until recently; and (2) the South, where control measures have caused a dramatic decline in numbers of cases since 1990. Polymorphism in non-repeat regions of antigen-encoding loci was dramatically reduced in the South compared to the NW. These results suggest a two-pronged strategy for malaria eradication: (1) strenuous non-vaccine control measures that will cause a severe population bottleneck in the parasite; and (2) a subsequent local vaccine focused on one or a few locally occurring alleles at antigen-encoding loci.
疟原虫感染阶段的一些细胞表面抗原已被提议作为疫苗候选物,但编码这些抗原的基因座的高水平多态性对疫苗的有效性是一个问题。为了检测抗疟控制措施(包括药物和病媒控制)对抗原编码基因座多态性的影响,我们分析了 2006 年至 2007 年在泰国两个地区采集的四种疟原虫 vivax 和两种疟原虫 falciparum 的四个抗原编码基因座的序列:(1)西北,直到最近疟疾病例一直居高不下;(2)南部,自 1990 年以来,控制措施导致病例数量急剧下降。与西北相比,南部抗原编码基因座中非重复区的多态性明显降低。这些结果表明了一种双管齐下的疟疾消除策略:(1)采取严格的非疫苗控制措施,这将导致寄生虫严重的种群瓶颈;(2)随后在抗原编码基因座上针对一个或几个当地出现的等位基因进行局部疫苗接种。