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家族之事:变异基因、PfEMP1结合与疟疾疾病

A family affair: var genes, PfEMP1 binding, and malaria disease.

作者信息

Kraemer Susan M, Smith Joseph D

机构信息

Seattle Biomedical Research Institute, Seattle, WA 98109-5219, USA.

出版信息

Curr Opin Microbiol. 2006 Aug;9(4):374-80. doi: 10.1016/j.mib.2006.06.006. Epub 2006 Jun 30.

Abstract

An immunovariant adhesion protein family in Plasmodium falciparum named erythrocyte membrane protein 1 (PfEMP1), encoded by var genes, is responsible for both antigenic variation and cytoadhesion of infected erythrocytes at blood microvasculature sites throughout the body. Elucidation of the genome sequence of P. falciparum has revealed that var genes can be classified into different groups, each with distinct 5' flanking sequences, chromosomal locations and gene orientations. Recent binding and serological comparisons suggest that this genomic organization might cause var genes to diversify into separately recombining adhesion groups that have different roles in infection and disease. Detailed understanding of PfEMP1 expression and receptor binding mechanisms during infection and of the antigenic relatedness of disease variants might lead to new approaches in prevention of malaria disease.

摘要

恶性疟原虫中一个名为红细胞膜蛋白1(PfEMP1)的免疫变异黏附蛋白家族,由var基因编码,负责感染红细胞在全身血液微血管部位的抗原变异和细胞黏附。恶性疟原虫基因组序列的阐明表明,var基因可分为不同的组,每组具有不同的5'侧翼序列、染色体位置和基因方向。最近的结合和血清学比较表明,这种基因组组织可能导致var基因多样化,形成在感染和疾病中具有不同作用的独立重组黏附组。深入了解感染期间PfEMP1的表达和受体结合机制以及疾病变体的抗原相关性,可能会带来预防疟疾的新方法。

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