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首页> 外文期刊>BMC Infectious Diseases >Plasmodium falciparum malaria parasite var gene expression is modified by host antibodies: longitudinal evidence from controlled infections of Kenyan adults with varying natural exposure
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Plasmodium falciparum malaria parasite var gene expression is modified by host antibodies: longitudinal evidence from controlled infections of Kenyan adults with varying natural exposure

机译:恶性疟原虫疟原虫var基因表达被宿主抗体修饰:来自肯尼亚成年人自然暴露量不同的受控感染的纵向证据

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Background The PfEMP1 family of Plasmodium falciparum antigens play a key role in pathogenesis of severe malaria through their insertion into the surface of parasite infected erythrocytes, and adhesion to host cells. Previous studies have suggested that parasites expressing PfEMP1 subclasses group A and DC8, associated with severe malaria, may have a growth advantage in immunologically na?ve individuals. However, this idea has not been tested in longitudinal studies. Methods Here we assessed expression of the var genes encoding PfEMP1, in parasites sampled from volunteers with varying prior exposure to malaria, following experimental infection by sporozoites (PfSPZ). Using qPCR, we tested for associations between the expression of various var subgroups in surviving parasite populations from each volunteer and 1) the levels of participants’ antibodies to infected erythrocytes before challenge infection and 2) the apparent in vivo parasite multiplication rate. Results We show that 1) expression of var genes encoding for group A and DC8-like PfEMP1 were associated with low levels of antibodies to infected erythrocytes (αIE) before challenge, and 2) expression of a DC8-like CIDRα1.1 domain was associated with higher apparent parasite multiplication rate in a manner that was independent of levels of prior antibodies to infected erythrocytes. Conclusions This study provides insight into the role of antibodies to infected erythrocytes surface antigens in the development of naturally acquired immunity and may help explain why specific PfEMP1 variants may be associated with severe malaria. Trial registration Pan African Clinical Trial Registry: PACTR201211000433272 . Date of registration: 10th October 2012.
机译:背景恶性疟原虫抗原的PfEMP1家族通过将其插入寄生虫感染的红细胞表面并粘附于宿主细胞,在严重疟疾的发病机理中起关键作用。先前的研究表明,表达PfEMP1亚类A和DC8的寄生虫与严重的疟疾有关,在免疫上幼稚的个体中可能具有生长优势。但是,这种想法尚未在纵向研究中得到检验。方法在这里,我们评估了在被子孢子虫(PfSPZ)实验感染后,从先前有不同疟疾暴露水平的志愿者身上采集的寄生虫中编码PfEMP1的var基因的表达。使用qPCR,我们测试了每个志愿者在存活的寄生虫种群中各个var亚组的表达与1)攻击感染前参与者对被感染红细胞的抗体水平以及2)表观体内寄生虫繁殖率之间的关联。结果我们显示:1)攻击前编码A组和DC8样PfEMP1的var基因表达与感染的红细胞(αIE)抗体水平低相关; 2)DC8样CIDRα1.1结构域的表达相关具有较高的表观寄生虫繁殖率,且其方式与先前针对感染的红细胞的抗体水平无关。结论这项研究提供了关于感染的红细胞表面抗原抗体在自然获得性免疫发展中的作用的见解,并可能有助于解释为什么特定的PfEMP1变异体可能与严重的疟疾有关。试用注册泛非临床试验注册:PACTR201211000433272。注册日期:2012年10月10日。

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