Cited by 3Malaria Research and ControlBlood groups and transfusionVector-borne infectious diseases

Antibody Responses to Plasmodium falciparum and Plasmodium vivax and Prospective Risk of Plasmodium spp. Infection Postpartum

Open access
McLean, Alistair R. D., Boel, Machteld, McGready, Rose, Ataide, Ricardo, Drew, Damien, Tsuboi, Takafumi, Beeson, James G., Nosten, François +2 more·2017·The American Society of Tropical Medicine and Hygiene

Abstract

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.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.4269/ajtmh.16-0690

Cites

33 of 33 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • 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 measured
  • Sequestration 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)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Cited by

Sorted by citations

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.
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
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
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

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review