
Plasmodium vivax is the most widespread malaria parasite worldwide, with up to 2,000,000,000 people at risk of infection. As well as causing illness and death in its “active” stage of infection, the parasite can hide as hypnozoites, a dormant stage, in the liver, and is a significant cause of “relapsing” malaria. These hypnozoites, undetectable with current diagnostics, can be responsible for >80% of all blood-stage infections. Identifying and targeting individuals with hypnozoites is thus essential for accelerating and achieving malaria elimination. A major gap in the P. vivax elimination toolkit is the identification of individuals carrying clinically silent and undetectable hypnozoites. The current study developed a panel of serological exposure markers capable of classifying individuals with P. vivax infections within the previous nine months who have a high likelihood of harboring hypnozoites. Using the Perkin-Elmer AlphaScreen system (https://www.perkinelmer.com/Content/RelatedMaterials/Brochures/BRO_AlphaScreen2004.pdf), the researchers measured IgG antibody responses to 342 P. vivax proteins expressed by a wheat germ cell-free system, invented at Ehime University in Japan, in longitudinal clinical cohorts conducted in Thailand and Brazil, and identified 60 candidate serological markers of exposure. Candidate markers were then validated using samples from year-long observational cohorts conducted in Thailand, Brazil, and the Solomon Islands and antibody responses to eight P. vivax proteins classified P. vivax infections in the previous 9 months with 80% sensitivity and specificity. Mathematical models demonstrate that a serological testing and treatment strategy based on testing for responses to these eight
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