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Updated: Feb 10, 2026

Measuring Naturally Acquired Phagocytosis-Inducing Antibodies to Plasmodium falciparum Parasites by a Flow Cytometry-Based Assay
Published on: August 6, 2020
The naturally acquired immunity in severe malaria and its implication for a PfEMP-1 based vaccine
1Department of Parasitology, Mycology and Environmental Microbiology, Swedish Institute for Infectious Disease Control, Sweden. qijun.chen@smi.ki.se
Abstract:
Malaria vaccine development has so far been largely focused on antigens involved in parasite invasion pathways rather than on antigens associated with severe disease and naturally acquired immunity. Individuals repeatedly exposed to Plasmodium falciparum will eventually become immune to severe disease. Parasite-derived antigens expressed on the infected red blood cell (iRBC) surface are the main targets of protective immunity and can be explored as a rational alternative in development of an anti-malaria vaccine.
Insights
Developing a malaria vaccine requires focusing on antigens linked to severe disease and immunity. Targeting parasite antigens on infected red blood cells offers a promising strategy for effective malaria vaccines.
Area of Science:
- Immunology
- Parasitology
- Vaccinology
Background:
- Current malaria vaccine research primarily targets parasite invasion pathways.
- Naturally acquired immunity to severe Plasmodium falciparum malaria develops after repeated exposure.
Purpose of the Study:
- To explore parasite-derived antigens on infected red blood cells as potential vaccine targets.
- To shift vaccine development focus towards antigens associated with severe disease and immunity.
Main Methods:
- Analysis of immune responses to Plasmodium falciparum infection.
- Identification of parasite antigens expressed on the surface of infected red blood cells.
Main Results:
- Antigens on the infected red blood cell surface are key targets of protective immunity.
- Naturally acquired immunity correlates with exposure to these surface antigens.
Conclusions:
- Antigens expressed on the infected red blood cell surface represent a rational target for malaria vaccine development.
- This approach may lead to more effective vaccines against severe malaria.
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