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Origins and evolution of antigenic diversity in malaria parasites.

机译:疟原虫中抗原多样性的起源和进化。

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Each year, malaria parasites cause more than 500 million infections and 0.5-3 million deaths worldwide, mostly among children under five living in sub-Saharan Africa. In contrast with several viral and bacterial pathogens, which elicit long-lived immunity after a primary infection, these parasites require several years of continuous exposure to confer partial, usually non-sterilizing immune protection. One of the main obstacles to the acquisition of antimalarial immunity is the high degree of antigenic diversity in potential target antigens, which enables parasites to evade immune responses elicited by past exposure to variant forms of the same antigen. Allelic polymorphism, the existence of genetically stable alternative forms of antigen-coding genes, originates from nucleotide replacement mutations and intragenic recombination. In addition, malaria parasites display antigenic variation, whereby a clonal lineage of parasites expresses successively alternate forms of an antigen without changes in genotype. This review focuses on molecular and evolutionary processes that promote allelic polymorphism and antigenic variation in natural malaria parasite populations and their implications for naturally acquired immunity and vaccine development.
机译:每年,疟疾寄生虫在全世界造成超过5亿例感染,0.5-300万例死亡,其中大多数是生活在撒哈拉以南非洲五岁以下儿童中。与几种病毒和细菌病原体相比,它们在初次感染后会引发长期的免疫力,而这些寄生虫则需要连续暴露数年,才能提供部分的,通常是非灭菌的免疫保护。获得抗疟疾免疫力的主要障碍之一是潜在靶抗原中高度的抗原多样性,这使得寄生虫能够逃避过去暴露于相同抗原变体形式引起的免疫反应。等位基因多态性是抗原编码基因的遗传稳定替代形式的存在,其起因于核苷酸置换突变和基因内重组。另外,疟原虫显示出抗原变异,由此寄生虫的克隆谱系连续表达抗原的其他形式,而基因型不变。这篇综述的重点是促进天然疟疾寄生虫种群中等位基因多态性和抗原变异的分子和进化过程,以及它们对自然获得性免疫和疫苗开发的影响。

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