Abstract

Antibodies to selected Plasmodium falciparum merozoite antigens are often reported to be associated with protection from malaria in one epidemiological cohort, but not in another. Here, we sought to understand this paradox by exploring the hypothesis that a threshold concentration of antibodies is necessary for protection. We analyzed data from two independent cohorts along the Kenyan coast, one in which antibodies to AMA1, MSP-2 and MSP-3 were associated with protection from malaria (Chonyi) and another in which this association was not observed (Junju). We used a malaria reference reagent to standardize antibody measurements across both cohorts, and applied statistical methods to derive the threshold concentration of antibodies against each antigen that best correlated with a reduced risk of malaria (the protective threshold), in the Chonyi cohort. We then tested whether antibodies in Junju reached the protective threshold concentrations observed in the Chonyi cohort. Except for children under 3 years, the age-matched proportions of children achieving protective threshold concentrations of antibodies against AMA1 and MSP-2 were significantly lower in Junju compared to Chonyi (Fishers exact test, P<0.01). For MSP-3, this difference was significant only among 4–5 year olds. We conclude that although antibodies are commonly detected in malaria endemic populations, they may be present in concentrations that are insufficient for protection. Our results have implications for the analysis and interpretation of similar data from immuno-epidemiological studies.

Highlights

  • Antibodies play an important role in mediating protection against clinical malaria

  • Using the purified IgG as a standard for measuring relative antibody concentrations, we determined for each antigen, the relative IgG antibody concentration that best correlated with protection from malaria by selecting the model with the least log pseudolikelihood [31]

  • An increasing body of evidence suggests that protection from malaria is dependent on high antibody concentrations [5,6,7,8,9,10]

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Summary

Introduction

Antibodies play an important role in mediating protection against clinical malaria. Immuno-epidemiological studies are widely used to assess the potential protective efficacy of antibodies against Plasmodium falciparum antigens in humans. Such studies have often yielded inconsistent results with some studies demonstrating a protective role for antibodies to a specific antigen, while others do not [4]. While there is reasonable agreement that high levels of antibodies are better indicators of protection than sero-positivity, the definition of “high” varies considerably between studies [5,6,7,8,9,10], making it difficult to compare findings from different sites

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