4.2 Article

Serology for Plasmodium vivax surveillance: A novel approach to accelerate towards elimination

Journal

PARASITOLOGY INTERNATIONAL
Volume 87, Issue -, Pages -

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.parint.2021.102492

Keywords

Malaria; Plasmodium vivax; Multiplex assay; Surveillance; Malaria elimination; Naturally acquired immunity

Categories

Funding

  1. National Health and Medical Research Council (NHMRC) [GNT #173210]
  2. Department of Foreign Affairs and Trade (DFAT)
  3. NHMRC [1043345, 1092789]
  4. Australian Centre for Research Excellence in Malaria Elimination (ACREME)
  5. National Health and Medical Research Council of Australia [1092789] Funding Source: NHMRC

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Plasmodium vivax is the most prevalent cause of human malaria worldwide, and despite efforts to control the disease, case reduction rates have decreased in recent years. Surveillance of malaria transmission levels is crucial, with serological tools providing valuable insights especially as transmission declines. Antibodies can remain in the host system for extended periods after parasite clearance, highlighting the importance of understanding antibody longevity and measuring antibodies to multiple antigens for accurate assessment of population exposure and immune status.
Plasmodium vivax is the most widespread causative agent of human malaria in the world. Despite the ongoing implementation of malaria control programs, the rate of case reduction has declined over the last 5 years. Hence, surveillance of malaria transmission should be in place to identify and monitor areas that require intensified malaria control interventions. Serological tools may offer additional insights into transmission intensity over parasite and entomological measures, especially as transmission levels decline. Antibodies can be detected in the host system for months to even years after parasite infections have been cleared from the blood, enabling malaria exposure history to be captured. Because the Plasmodium parasite expresses more than 5000 proteins, it is important to a) understand antibody longevity following infection and b) measure antibodies to more than one antigen in order to accurately inform on the exposure and/or immune status of populations. This review summarises current practices for surveillance of P. vivax malaria, the current state of research into serological exposure markers and their potential role for accelerating malaria elimination, and discusses further studies that need to be undertaken to see such technology implemented in malaria-endemic areas.

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