Estimation of Recent and Long-Term Malaria Transmission in a Population by Antibody Testing to Multiple Plasmodium falciparum Antigens

Background. Tools that estimate recent and long-term malaria transmission in a population would be highly useful for malaria elimination programs. Methods. The prevalence of antibodies to 11 Plasmodium falciparum antigens was assessed by cytometric bead assay or enzyme-linked immunosorbent assay in...

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Veröffentlicht in:The Journal of infectious diseases 2014-10, Vol.210 (7), p.1123-1132
Hauptverfasser: Ondigo, Bartholomew N., Hodges, James S., Ireland, Kathleen F., Magak, Ng'wena G., Lanar, David E., Dutta, Sheetij, Narum, David L., Park, Gregory S., Ofulla, Ayub V., John, Chandy C.
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Sprache:eng
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Zusammenfassung:Background. Tools that estimate recent and long-term malaria transmission in a population would be highly useful for malaria elimination programs. Methods. The prevalence of antibodies to 11 Plasmodium falciparum antigens was assessed by cytometric bead assay or enzyme-linked immunosorbent assay in 1000 people in a highland area of Kenya over 14 months, during a period of interrupted malaria transmission. Results. Antibodies differed by antigen in acquisition with age: rapid (> 80% antibody positive by age 20 years, 5 antigens), moderate (> 40% positive by age 20 years, 3 antigens), or slow (< 40% positive by age 20 years, 3 antigens). Antibody seroreversion rates in the 14 months between samples decreased with age rapidly (7 antigens), slowly (3 antigens), or remained high at all ages (schizont extract). Estimated antibody half-lives in individuals > 10 years of age were long (40 to > 80 years) for 5 antigens, moderate (5-20 years) for 3 antigens, and short (< 1 year) for 3 antigens. Conclusions. Antibodies to P. falciparum antigens in malaria-endemic areas vary by age, antigen, and time since last exposure to P. falciparum. Multiplex P. falciparum antibody testing could provide estimates of long-term and recent malaria transmission and potentially of a population's susceptibility to future clinical malaria.
ISSN:0022-1899
1537-6613
DOI:10.1093/infdis/jiu225