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Type: Journal article
Title: The Plasmodium falciparum erythrocyte invasion ligand Pfrh4 as a target of functional and protective human antibodies against malaria
Author: Reiling, L.
Richards, J.
Fowkes, F.
Wilson, D.
Chokejindachai, W.
Barry, A.
Tham, W.
Stubbs, J.
Langer, C.
Donelson, J.
Michon, P.
Tavul, L.
Crabb, B.
Siba, P.
Cowman, A.
Mueller, I.
Beeson, J.
Citation: PLoS One, 2012; 7(9):e45253-1-e45253-12
Publisher: Public Library of Science
Issue Date: 2012
ISSN: 1932-6203
Statement of
Linda Reiling, Jack S. Richards, Freya J. I. Fowkes, Danny W. Wilson, Watcharee Chokejindachai, Alyssa E. Barry, Wai-Hong Tham, Janine Stubbs, Christine Langer, John Donelson, Pascal Michon, Livingstone Tavul, Brendan S. Crabb, Peter M. Siba, Alan F. Cowman, Ivo Mueller, James G. Beeson
Abstract: Background: Acquired antibodies are important in human immunity to malaria, but key targets remain largely unknown. Plasmodium falciparum reticulocyte-binding-homologue-4 (PfRh4) is important for invasion of human erythrocytes and may therefore be a target of protective immunity. Methods: IgG and IgG subclass-specific responses against different regions of PfRh4 were determined in a longitudinal cohort of 206 children in Papua New Guinea (PNG). Human PfRh4 antibodies were tested for functional invasion-inhibitory activity, and expression of PfRh4 by P. falciparum isolates and sequence polymorphisms were determined. Results: Antibodies to PfRh4 were acquired by children exposed to P. falciparum malaria, were predominantly comprised of IgG1 and IgG3 subclasses, and were associated with increasing age and active parasitemia. High levels of antibodies, particularly IgG3, were strongly predictive of protection against clinical malaria and high-density parasitemia. Human affinity-purified antibodies to the binding region of PfRh4 effectively inhibited erythrocyte invasion by P. falciparum merozoites and antibody levels in protected children were at functionally-active concentrations. Although expression of PfRh4 can vary, PfRh4 protein was expressed by most isolates derived from the cohort and showed limited sequence polymorphism. Conclusions: Evidence suggests that PfRh4 is a target of antibodies that contribute to protective immunity to malaria by inhibiting erythrocyte invasion and preventing high density parasitemia. These findings advance our understanding of the targets and mechanisms of human immunity and evaluating the potential of PfRh4 as a component of candidate malaria vaccines
Keywords: Erythrocytes; Animals; Humans; Plasmodium falciparum; Parasitemia; Malaria, Falciparum; Immunoglobulin G; Membrane Proteins; Protozoan Proteins; Recombinant Fusion Proteins; Malaria Vaccines; Antibodies, Protozoan; Antigens, Protozoan; Gene Expression; Protein Binding; Polymorphism, Genetic; Adolescent; Child; Child, Preschool; Female; Male; Merozoites; Immunity, Humoral
Rights: © Reiling et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
RMID: 0020138022
DOI: 10.1371/journal.pone.0045253
Appears in Collections:Microbiology and Immunology publications

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