Abstract
BackgroundPlasmodium falciparum-infected erythrocytes (IE) sequester in deep vascular beds where their adhesion is mediated by an array of endothelial surface receptors. Because parasite adhesion has been associated with disease, antibodies that block this activity may confer protective immunity. Here, levels of plasma anti-adhesion activity and surface reactivity against freshly collected IEs from malaria-infected children were measured in a Malian birth cohort and related to child age and malaria infection history.MethodsPlasma samples from children enrolled at birth in a longitudinal cohort study of mother–infant pairs in Ouelessebougou, Mali were collected at multiple time points during follow-up visits. Anti-adhesion antibodies (i.e., inhibit IE binding to any of several endothelial receptors) and reactivity with surface IE proteins were measured using a binding inhibition assay and by flow cytometry, respectively.ResultsLevels of antibodies that inhibit the binding of children’s IE to the receptors ICAM-1, integrin α3β1 and laminin increased with age. The breadth of antibodies that inhibit ICAM-1 and laminin adhesion (defined as the proportion of IE isolates whose binding was reduced by ≥ 50%) also significantly increased with age. The number of malaria infections prior to plasma collection was associated with levels of plasma reactivity to IE surface proteins, but not levels of anti-adhesion activity.ConclusionsAge is associated with increased levels of antibodies that reduce adhesion of children’s IE to three of the ten endothelial receptors evaluated here. These results suggest that anti-adhesion antibodies to some but not all endothelial receptors are acquired during the first few years of life.
Highlights
Plasmodium falciparum-infected erythrocytes (IE) sequester in deep vascular beds where their adhesion is mediated by an array of endothelial surface receptors
Study population Anti-adhesion and IE surface-reactive antibodies were measured in plasma samples collected from Malian children participating in longitudinal cohort studies
Plasma samples were tested for inhibiting IE adhesion to the following receptors: CD36, intercellular adhesion molecule-1 (ICAM-1), P-selectin, platelet endothelial cell adhesion molecule-1 (PECAM-1/CD31), integrin α3β1, integrin α5β1, integrin αvβ3, laminin, cellular fibronectin and JAM-B
Summary
Plasmodium falciparum-infected erythrocytes (IE) sequester in deep vascular beds where their adhesion is mediated by an array of endothelial surface receptors. Because parasite adhesion has been associated with disease, antibodies that block this activity may confer protective immunity. Among the five human malaria parasites, Plasmodium falciparum is able to sequester in deep vascular beds of various tissues. Acquisition of antibodies to IE surface proteins that block parasite adhesion have been associated with improved outcomes, including reduction in infection, parasite density, increased birthweight, gestational age and maternal haemoglobin levels [27,28,29,30,31]. Previous studies from areas of stable malaria transmission reported that antibody levels to surface IE proteins are low in children aged 6–36 months [32, 33], and levels increase with age [33,34,35]. Age was associated with increased IE agglutination activity [36]
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