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Circulating Monocytes, Tissue Macrophages, and Malaria.

Nida Ozarslan1, Joshua F Robinson2, Stephanie L Gaw2,3

  • 1Marmara University School of Medicine, Istanbul, Turkey.

Journal of Tropical Medicine
|October 31, 2019
PubMed
Summary
This summary is machine-generated.

Malaria infection involves the Plasmodium parasite interacting with monocytes and macrophages in various organs. This review explores these interactions and their impact on malaria outcomes.

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Area of Science:

  • Immunology
  • Infectious Diseases
  • Parasitology

Background:

  • Malaria remains a major global health burden, causing significant morbidity and mortality.
  • The Plasmodium parasite exhibits a complex life cycle involving mosquito, liver, and blood stages.
  • Blood-stage malaria can target organs like the brain and placenta.

Purpose of the Study:

  • To review the interactions between Plasmodium parasites and monocytes/macrophages.
  • To summarize knowledge on malaria's effects on specific immune cells in key organs.
  • To highlight potential roles of these interactions in disease outcomes and suggest future research directions.

Main Methods:

  • Literature review of current knowledge on malaria and immune cell interactions.
  • Focus on monocytes and tissue-specific macrophages (Kupffer cells, microglia, placental macrophages).
  • Analysis of cellular and molecular changes resulting from parasite-immune cell interactions.

Main Results:

  • Plasmodium parasites interact with monocytes and macrophages during various life cycle stages and in affected organs.
  • These interactions induce changes in immune cells, including cytokine release and receptor expression.
  • Specific immune cells discussed include Kupffer cells (liver), microglia (CNS), and placental macrophages.

Conclusions:

  • Monocytes and macrophages play crucial roles in modulating malaria infection outcomes.
  • Understanding these host-parasite interactions is vital for developing effective malaria control strategies.
  • Further research is needed to fully elucidate the complex interplay between malaria and the innate immune system.