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Acquisition of naturally occurring antibody responses to recombinant protein domains of Plasmodium falciparum erythrocyte membrane protein I

Abstract:
Background: Antibodies targeting variant antigens expressed on the surface of Plasmodium falciparum infected erythrocytes have been associated with protection from clinical malaria. The precise target for these antibodies is unknown. The best characterized and most likely target is the erythrocyte surface-expressed variant protein family Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1). Methods: Using recombinant proteins corresponding to five domains of the expressed A4 var gene, A4 PfEMP1, the naturally occurring antibody response was assessed, by ELISA, to each domain in serum samples obtained from individuals resident in two communities of differing malaria transmission intensity on the Kenyan coast. Using flow cytometry, the correlation in individual responses to each domain with responses to intact A4-infected erythrocytes expressing A4 PfEMP1 on their surface as well as responses to two alternative parasite clones and one clinical isolate was assessed. Results: Marked variability in the prevalence of responses between each domain and between each transmission area was observed, as wasa strong correlation between age and reactivity with some but not all domains. Individual responses to each domain varied strikingly, with some individuals showing reactivity to all domains and others with no reactivity to any, this was apparent at all age groups. Evidence for possible cross-reactivity in responses to the domain DBL4γ was found. Conclusion: Individuals acquire antibodies to surface expressed domains of a highly variant protein. The finding of potential cross-reactivity in responses to one of these domains is an important initial finding in the consideration of potential vaccine targets.
Publication status:
Published
Peer review status:
Peer reviewed

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Institution:
"Kenya Medical Research Institute Centre for Geographic Medicine Research Coast (KEMRI-CGMRC), Kilifi, Kenya", "University of Oxford"
Research group:
Molecular Parasitology Group
Department:
Medical Sciences Division - Clinical Medicine,Nuffield Department of - NDM John Radcliffe
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
Weatherall Insti. of Molecular Medicine
Research group:
Molecular Parasitology Group
Role:
Author
More by this author
Institution:
"Kenya Medical Research Institute Centre for Geographic Medicine Research Coast (KEMRI-CGMRC), Kilifi, Kenya"
Role:
Author
More by this author
Institution:
"Kenya Medical Research Institute Centre for Geographic Medicine Research Coast (KEMRI-CGMRC), Kilifi, Kenya"
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
Weatherall Insti. of Molecular Medicine
Research group:
Molecular Parasitology Group
Role:
Author


More from this funder
Funding agency for:
Mwangi, T
Mackintosh, C
Marsh, K
Newbold, C


Publisher:
BioMed Central
Journal:
Malaria Journal More from this journal
Volume:
7
Article number:
155
Publication date:
2008-08-01
Edition:
Publisher's version
DOI:
ISSN:
1475-2875


Language:
English
Subjects:
UUID:
uuid:7343bdea-b880-4e42-ac75-05c56f3b41cb
Local pid:
ora:3079
Deposit date:
2009-11-25

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