Ontology highlight
ABSTRACT:
Methods: This retrospective study utilized plasma samples collected longitudinally at six time points from children aged one to five years. Multiplex assays were used to measure antibody levels against four P. falciparum AMA 1 variants (from the 3D7, FVO, HB3 and CAMP parasite strains) and the 3D7 variant of the EBA 175 region II antigen and the levels compared between symptomatic and asymptomatic children. The relative proportions of cross-reactive and strain-specific antibodies against the four AMA 1 variants per sampling time point were assessed by Bland-Altman plots. The levels of antibodies against allelic AMA1 variants, measured by singleplex and multiplex luminex assays, were also compared.
Results: The data show that increased transmission intensity is associated with higher levels of cross-reactive antibody responses, most likely a result of a greater proportion of multiple parasite clone infections during the high transmission period. Anti-AMA1 antibodies were however associated with a history of infection rather than protection in this age group.
Conclusion: The data contribute to understanding the underlying mechanism of the acquisition of strain-transcending antibody immunity following repeated exposure to diverse parasite strains.
SUBMITTER: Kusi KA
PROVIDER: S-EPMC5612719 | biostudies-literature | 2017
REPOSITORIES: biostudies-literature
Kusi Kwadwo A KA Manu Emmanuel A EA Manful Gwira Theresa T Kyei-Baafour Eric E Dickson Emmanuel K EK Amponsah Jones A JA Remarque Edmond J EJ Faber Bart W BW Kocken Clemens H M CHM Dodoo Daniel D Gyan Ben A BA Awandare Gordon A GA Atuguba Frank F Oduro Abraham R AR Koram Kwadwo A KA
PloS one 20170925 9
<h4>Introduction</h4>Plasmodium falciparum induced antibodies are key components of anti-malarial immunity in malaria endemic areas, but their antigen targets can be polymorphic. Induction of a high proportion of strain-specific antibodies will limit the recognition of a broad diversity of parasite strains by these responses. There are indications that circulating parasite diversity varies with malaria transmission intensity, and this may affect the specificity of elicited anti-malarial antibodi ...[more]