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The merozoite surface protein 1 (MSP1) is the most abundant protein on the surface of the invasive merozoite stages of Plasmodium falciparum and has long been considered a key target of protective immunity. We used samples from a single controlled human malaria challenge study to test whether the full-length version of MSP1 (MSP1FL) induced antibodies that mediated Fc-IgG functional activity in five independent assays. We found that anti-MSP1FL antibodies induced complement fixation via C1q, monocyte-mediated phagocytosis, neutrophil respiratory burst, and natural killer cell degranulation as well as IFNγ production. Activity in each of these assays was strongly associated with protection. The breadth of MSP1-specific Fc-mediated effector functions was more strongly associated with protection than the individual measures and closely mirrored what we have previously reported using the same assays against merozoites. Our findings suggest that MSP1FL is an important target of functional antibodies that contribute to a protective immune response against malaria.

Original publication

DOI

10.26508/lsa.202301910

Type

Journal

Life science alliance

Publication Date

08/2024

Volume

7

Addresses

https://ror.org/013czdx64 Centre of Infectious Diseases, Heidelberg University Hospital, Heidelberg, Germany micha.rosenkranz@web.de.

Keywords

Neutrophils, Killer Cells, Natural, Humans, Plasmodium falciparum, Malaria, Falciparum, Immunoglobulin G, Merozoite Surface Protein 1, Antibodies, Protozoan, Phagocytosis, Female, Merozoites, Interferon-gamma