| Literature DB >> 17015460 |
Louise Joergensen1, Louise Turner, Pamela Magistrado, Madeleine A Dahlbäck, Lasse S Vestergaard, John P Lusingu, Martha Lemnge, Ali Salanti, Thor G Theander, Anja T R Jensen.
Abstract
The var gene-encoded Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) family is responsible for antigenic variation and sequestration of infected erythrocytes during malaria. We have previously grouped the 60 PfEMP1 variants of P. falciparum clone 3D7 into groups A and B/A (category A) and groups B, B/C, and C (category non-A). Expression of category A molecules is associated with severe malaria, and that of category non-A molecules is associated with uncomplicated malaria and asymptomatic infection. Here we assessed cross-reactivity among 60 different recombinant PfEMP1 domains derived from clone 3D7 by using a competition enzyme-linked immunosorbent assay and a pool of plasma from 63 malaria-exposed Tanzanian individuals. We conclude that naturally acquired antibodies are largely directed toward epitopes varying between different domains with a few, mainly category A, domains sharing cross-reactive antibody epitopes. Identification of groups of serological cross-reacting molecules is pivotal for the development of vaccines based on PfEMP1.Entities:
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Year: 2006 PMID: 17015460 PMCID: PMC1698063 DOI: 10.1128/IAI.01187-06
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441