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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/29177
Title: Evidence that the erythrocyte invasion ligand PfRh2 is a target of protective immunity against Plasmodium falciparum malaria
Authors: Linda Reiling
Jack S. Richards
Freya J.I. Fowkes
Alyssa E. Barry
Tony Triglia
Watcharee Chokejindachai
Pascal Michon
Livingstone Tavul
Peter M. Siba
Alan F. Cowman
Ivo Mueller
James G. Beeson
Walter and Eliza Hall Institute of Medical Research
University of Melbourne
Burnet Institute
Mahidol University
Papua New Guinea Institute of Medical Research
Keywords: Immunology and Microbiology
Issue Date: 15-Nov-2010
Citation: Journal of Immunology. Vol.185, No.10 (2010), 6157-6167
Abstract: Abs targeting blood-stage Ags of Plasmodium falciparum are important in acquired immunity to malaria, but major targets remain unclear. The P. falciparum reticulocyte-binding homologs (PfRh) are key ligands used by merozoites during invasion of erythrocytes. PfRh2a and PfRh2b are functionally important members of this family and may be targets of protective immunity, but their potential role in human immunity has not been examined. We expressed eight recombinant proteins covering the entire PfRh2 common region, as well as PfRh2a-and PfRh2b-specific regions. Abs were measured among a cohort of 206 Papua New Guinean children who were followed prospectively for 6 mo for reinfection and malaria. At baseline, Abs were associated with increasing age and active infection. High levels of IgG to all PfRh2 protein constructs were strongly associated with protection from symptomatic malaria and high-density parasitemia. The predominant IgG subclasses were IgG1 and IgG3, with little IgG2 and IgG4 detected. To further understand the significance of PfRh2 as an immune target, we analyzed PfRh2 sequences and found that polymorphisms are concentrated in an N-terminal region of the protein and seem to be under diversifying selection, suggesting immune pressure. Cluster analysis arranged the sequences into two main groups, suggesting that many of the haplotypes identified may be antigenically similar. These findings provide evidence suggesting that PfRh2 is an important target of protective immunity in humans and that Abs act by controlling blood-stage parasitemia and support its potential for vaccine development. Copyright © 2010 by The American Association of Immunologists, Inc.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=78650650970&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/29177
ISSN: 15506606
00221767
Appears in Collections:Scopus 2006-2010

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