Antibody Responses to Plasmodium falciparum and Plasmodium vivax and Prospective Risk of Plasmodium spp. Infection Postpartum
Open accessAbstract
Postpartum women may have an altered susceptibility to Plasmodium falciparum and Plasmodium vivax. The relationship between naturally acquired malarial immunity and susceptibility to malaria postpartum is yet to be determined. IgG levels were measured against P. falciparum and P. vivax antigens from delivery in 201 postpartum and 201 nonpregnant controls over 12 weeks. Associations between time-varying antibody levels and time to first microscopically confirmed species-specific infection were determined by Cox regression. Associations between antibody levels and prospective risk of Plasmodium infection were similar in postpartum and control women. A 2-fold increase in P. falciparum antibody levels was associated with increased prospective risk of P. falciparum infection (hazard ratio [HR] range = 1.37–1.94). Antibody levels against most P. vivax antigens displayed no association with prospective risk of P. vivax infection (HR range = 1.02–1.05) with the exception of Pv MSP1 19 antibodies that were weakly associated with prospective risk of P. vivax infection (HR = 1.14 (95% confidence interval = 1.02, 1.28) per 2-fold increase in levels). Associations between antibody levels and prospective risk of infection attenuated when adjusted for documented retrospective exposure. Serology may be a useful tool to predict and monitor women at increased risk of P. falciparum infection postpartum, particularly in the absence of a detailed history of retrospective infections.
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These knobs express PfEMP1, enabling infected cells to adhere to receptors on the capillary and venous endothelium, a process known as sequestration.
“These knobs express an adhesive protein called P.falciparum erythrocyte membrane protein 1 (PfEMP1), enabling the infected cells to adhere to receptors on the capillary and venous endothelium, a process known as sequestration.”
From Current update on malaria in pregnancy: a systematic review (2025) · cites this paper as [93]
The Introduction (page unavailable) says PfEMP1 is the predominant antigen on the surface of P. falciparum-infected erythrocytes and that a PfEMP1 variant mediates placental sequestration through adherence. It does not mention knobs or establish adhesion to receptors on capillary and venous endothelium. (LLM, conf=0.86)
Experimental — accuracy not yet measuredSequestration and rosette formation impair the spleen's ability to effectively clear infected erythrocytes, ultimately leading to organ dysfunction.
“This sequestration and the formation of “rosettes” (the adherence of infected erythrocytes to uninfected cells) impair the spleen's ability to effectively clear the infected erythrocytes, ultimately leading to organ dysfunction [92, 93].”
From Current update on malaria in pregnancy: a systematic review (2025) · cites this paper as [93]
The Introduction (page unavailable) says that a parasite protein mediates sequestration of infected erythrocytes in the placenta. It does not discuss rosette formation, impaired splenic clearance, or organ dysfunction, so it supports only the sequestration element of the cited sentence. (LLM, conf=0.84)
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Current update on malaria in pregnancy: a systematic review
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- Authors
- McLean, A. R. D., Boel, M., McGready, R., Ataide, R., Drew, D., Tsuboi, T., Beeson, J. G., Nosten, F., Simpson, J. A., & Fowkes, F. J. I.
- Affiliations
- Burnet Institute (AU)
- Mahidol University (TH)
- Macfarlane Burnet Institute of Medical Research, Melbourne, Australia.
- Ehime University (JP)
- The University of Melbourne (AU)
- Corresponding author
- Fowkes, Freya J. I.
- ORCID
- Venue
- The American Society of Tropical Medicine and Hygiene
- Published
- 2017-05-03
- Volume
- 96
- Issue
- 5
- Pages
- 1197-1204
- ISSN
- 0002-9637 (ISSN-L)
- 1476-1645
- PMC
- PMC5417217
- OpenAlex
- W2610947996
- Cited by
- 3
- References
- 33
- Citations by year
- 2026: 1 · 2025: 1 · 2018: 1
- FWCI
- 0.26
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- American Journal of Tropical Medicine and Hygiene (publishedVersion)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Monash University Research Portal (Monash University) (submittedVersion, other-oa)
- Minerva Access (University of Melbourne) (submittedVersion, cc-by)
- Greater South Information System
- Funders
- Burnet Institute
- University of Oxford
- Medical Research Council
- National Health and Medical Research Council
- Topics
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Malaria Research and Control
- Health Sciences › Medicine › Hematology › Blood groups and transfusion
- Life Sciences › Immunology and Microbiology › Parasitology › Vector-borne infectious diseases
- Keywords
- Plasmodium falciparum, Plasmodium vivax, antibody response, IgG, malaria susceptibility
- MeSH terms
- Artesunate, Antibodies, Protozoan, Antimalarials, Chloroquine, Disease Susceptibility, Female, Humans, Immunoglobulin G, Plasmodium falciparum, Plasmodium vivax, Pregnancy, Risk, Time Factors, Cohort Studies, Mefloquine, Proportional Hazards Models, Malaria, Falciparum, Malaria, Vivax, Parasitemia, Merozoite Surface Protein 1, Parturition, Artemisinins, Adaptive Immunity, Disease Resistance
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