Pasternak Noa D, Dzikowski Ron
Department of Microbiology and Molecular Genetics, The Institute for Medical Research Israel-Canada, Kuvin Center for the Study of Infectious and Tropical Diseases, The Hebrew University-Hadassah Medical School, Jerusalem, Israel.
Int J Biochem Cell Biol. 2009 Jul;41(7):1463-6. doi: 10.1016/j.biocel.2008.12.012. Epub 2008 Dec 25.
The deadliest form of human malaria is caused by the protozoan parasite Plasmodium falciparum affecting millions worldwide every year. P. falciparum virulence is attributed to its ability to evade the human immune system by modifying infected host red blood cells to adhere to the vascular endothelium and to undergo antigenic variation. The main antigenic ligands responsible for both cytoadherence and antigenic variation are members of the P. falciparum Erythrocyte Membrane Protein-1 (PfEMP1) family. These polymorphic proteins are encoded by a multi-copy gene family called var. Each individual parasite expresses a single var gene at a time, maintaining the remaining approximately 60 var genes found in its genome in a transcriptionally silent state. As the antibody response against the single expressed PfEMP1 develops, small sub-populations of parasites switch expression to alternative forms of PfEMP1 and re-establish the infection. Therefore, PfEMP1 is considered a key player in the pathogenicity of P. falciparum.
人类疟疾最致命的形式是由原生动物寄生虫恶性疟原虫引起的,每年影响全球数百万人。恶性疟原虫的毒力归因于其通过修饰受感染的宿主红细胞以粘附于血管内皮并进行抗原变异来逃避人类免疫系统的能力。负责细胞粘附和抗原变异的主要抗原配体是恶性疟原虫红细胞膜蛋白1(PfEMP1)家族的成员。这些多态性蛋白由一个名为var的多拷贝基因家族编码。每个单独的寄生虫一次只表达一个var基因,将其基因组中发现的其余约60个var基因保持在转录沉默状态。随着针对单一表达的PfEMP1的抗体反应的发展,一小部分寄生虫会将表达切换为PfEMP1的替代形式并重新建立感染。因此,PfEMP1被认为是恶性疟原虫致病性的关键因素。