# VAR2CSA-specific IgG and IgM antibodies are markers of exposure and protection against adverse malaria pregnancy outcomes

**Authors:** Akachukwu M. Onwuka, Elizabeth H. Aitken, Wina Hasang, Mwayiwawo Madanitsa, Victor Mwapasa, Kamija Phiri, Feiko O. ter Kuile, Stephen J. Rogerson

PMC · DOI: 10.1186/s12936-025-05773-0 · Malaria Journal · 2025-12-31

## TL;DR

This study shows that specific antibodies against VAR2CSA in pregnant women are linked to malaria exposure and can protect against harmful pregnancy outcomes like low birth weight and maternal anemia.

## Contribution

The study identifies VAR2CSA-specific IgG and IgM antibodies as novel markers for malaria exposure and protection during pregnancy.

## Key findings

- Women infected with malaria had higher VAR2CSA-specific antibody levels at enrollment compared to uninfected women.
- Higher IgG levels at delivery in uninfected women were associated with a lower risk of low birth weight.
- Higher IgM levels at enrollment in infected women were linked to reduced maternal anemia at delivery.

## Abstract

Placental malaria is caused by the binding of the Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) protein VAR2CSA, found on the surface of infected erythrocytes, to placental tissue. Complications include maternal anaemia, low birth weight, small for gestational age and preterm delivery. Acquisition of antibodies against VAR2CSA during pregnancy has been linked to immunity against infection.

Pregnant Malawian women were enrolled at their first antenatal care visit at 16–28 weeks’ gestation into a trial of malaria prevention. Women with malaria infection at enrolment (n = 321) or any later point in pregnancy (n = 145) were selected. The IgG and IgM plasma levels against the VAR2CSA DBL1X-ID2a domain were measured at enrolment and delivery. Associations between the DBL1X-ID2a VAR2CSA-specific IgG and IgM antibody levels at enrolment or delivery and low birth weight, small for gestational age, maternal anaemia at delivery, and preterm delivery were assessed using logistic regression with confounder adjustment.

Women with malaria infection at enrolment had higher antibody levels to DBL1X-ID2a than uninfected women, and these declined from enrolment to delivery. There were no significant associations between the IgG antibody level measured at enrolment and the birth outcomes of interest, but the IgG antibody level at delivery in women uninfected at enrolment was associated with a lower risk of low birth weight, adjusted odds ratio (aOR) 0.43 (95% CI 0.19–0.97) p = 0.04. Additionally, in women infected at enrolment, one log higher IgM antibodies to DBL1X-ID2a VAR2CSA at enrolment were associated with a significant 23% decrease in maternal anaemia at delivery, aOR 0.77 (95% CI 0.60–0.99), p = 0.04.

VAR2CSA-specific IgG and IgM antibodies are markers of malaria infection and protection against placental malaria outcomes.

The online version contains supplementary material available at 10.1186/s12936-025-05773-0.

## Linked entities

- **Diseases:** malaria (MONDO:0005136)
- **Species:** Plasmodium falciparum (taxon 5833)

## Full-text entities

- **Genes:** ID2 (inhibitor of DNA binding 2) [NCBI Gene 3398] {aka GIG8, ID2A, ID2H, bHLHb26}
- **Diseases:** malaria (MESH:D008288), preterm delivery (MESH:D047928), anaemia (MESH:D000743), infected (MESH:D007239)
- **Chemicals:** VAR2CSA (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC12866454/full.md

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Source: https://tomesphere.com/paper/PMC12866454