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Published on: July 11, 2025
Potential pharmacologic interventions targeting TLR signaling in placental malaria
Francis M Kobia1, Kaushik Maiti2, Moses M Obimbo3
1Directorate of Research and Innovation, Mount Kenya University, P.O. Box 342, 01000, Thika, Kenya; Centre for Malaria Elimination, Mount Kenya University, P.O. Box 342, 01000, Thika, Kenya.
Abstract:
Complications from placental malaria cause poor pregnancy outcomes, including low birthweight, preterm delivery, and stillbirths. Many of these complications are driven by maternal innate proinflammatory responses to the sequestration of Plasmodium falciparum in the placenta. However, recent studies show that, in reaction to maternal innate immune responses that are detrimental to the fetus, the fetus mounts innate immune counter-responses that ameliorate pregnancy outcomes. Such fetal-maternal conflict in placental malaria has potential for pharmacologic modulation for better pregnancy outcomes. Here, we discuss placental malaria pathogenesis, its complications, and the role of innate immunity and fetal-maternal innate immune conflict in placental malaria. Finally, we discuss pharmacologic immunomodulatory strategies and agents with the potential to improve placental malaria outcomes.

