Low prevalence of antibodies to preerythrocytic but not blood-stage Plasmodium falciparum antigens in an area of unstable malaria transmission compared to prevalence in an area of stable malaria transmission
Department of Quantitative Health Sciences; Department of Pediatrics
Medical Subject Headings
Adolescent; Adult; Aged; Animals; Antibodies, Protozoan; Antigens, Protozoan; Child; Child, Preschool; Enzyme-Linked Immunosorbent Assay; Female; Humans; Immunoglobulin G; Kenya; Malaria, Falciparum; Male; Middle Aged; Plasmodium falciparum; Prevalence
Biostatistics | Epidemiology | Health Services Research | Immunology and Infectious Disease | Pediatrics
In areas where levels of transmission of Plasmodium falciparum are high and stable, the age-related acquisition of high-level immunoglobulin G (IgG) antibodies to preerythrocytic circumsporozoite protein (CSP) and liver-stage antigen 1 (LSA-1) has been associated with protection from clinical malaria. In contrast, age-related protection from malaria develops slowly or not at all in residents of epidemic-prone areas with unstable low levels of malaria transmission. We hypothesized that this suboptimal clinical and parasitological immunity may in part be due to reduced antibodies to CSP or LSA-1 and/or vaccine candidate blood-stage antigens. Frequencies and levels of IgG antibodies to CSP, LSA-1, thrombospondin-related adhesive protein (TRAP), apical membrane antigen 1 (AMA-1), erythrocyte binding antigen 175 (EBA-175), and merozoite surface protein 1 (MSP-1) were compared in 243 Kenyans living in a highland area of unstable transmission and 210 residents of a nearby lowland area of stable transmission. Levels of antibodies to CSP, LSA-1, TRAP, and AMA-1 in the oldest age group (>40 years) in the unstable transmission area were lower than or similar to those of children 2 to 6 years old in the stable transmission area. Only 3.3% of individuals in the unstable transmission area had high levels of IgG (>2 arbitrary units) to both CSP and LSA-1, compared to 43.3% of individuals in the stable transmission area. In contrast, antibody levels to and frequencies of MSP-1 and EBA-175 were similar in adults in areas of stable and unstable malaria transmission. Suboptimal immunity to malaria in areas of unstable malaria transmission may relate in part to infrequent high-level antibodies to preerythrocytic antigens and AMA-1.
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Citation: Infect Immun. 2008 Dec;76(12):5721-8. Epub 2008 Sep 22. Link to article on publisher's site
Noland, Gregory S.; Hendel-Paterson, Brett; Min, Xinan M.; Moormann, Ann M.; Vulule, John M.; Narum, David L.; Lanar, David E.; Kazura, James W.; and John, Chandy C., "Low prevalence of antibodies to preerythrocytic but not blood-stage Plasmodium falciparum antigens in an area of unstable malaria transmission compared to prevalence in an area of stable malaria transmission" (2008). Quantitative Health Sciences Publications and Presentations. 404.