Circulating Monocytes, Tissue Macrophages, and Malaria.
Nida OzarslanJoshua F RobinsonStephanie L GawPublished in: Journal of tropical medicine (2019)
Malaria is a significant cause of global morbidity and mortality. The Plasmodium parasite has a complex life cycle with mosquito, liver, and blood stages. The blood stages can preferentially affect organs such as the brain and placenta. In each of these stages and organs, the parasite will encounter monocytes and tissue-specific macrophages-key cell types in the innate immune response. Interactions between the Plasmodium parasite and monocytes/macrophages lead to several changes at both cellular and molecular levels, such as cytokine release and receptor expression. In this review, we summarize current knowledge on the relationship between malaria and blood intervillous monocytes and tissue-specific macrophages of the liver (Kupffer cells), central nervous system (microglia), and placenta (maternal intervillous monocytes and fetal Hofbauer cells). We describe their potential roles in modulating outcomes from infection and areas for future investigation.
Keyphrases
- plasmodium falciparum
- immune response
- dendritic cells
- life cycle
- induced apoptosis
- peripheral blood
- cell cycle arrest
- healthcare
- signaling pathway
- cell death
- single cell
- endoplasmic reticulum stress
- inflammatory response
- multiple sclerosis
- toll like receptor
- mesenchymal stem cells
- stem cells
- neuropathic pain
- spinal cord
- body mass index
- resting state
- risk assessment
- preterm birth
- birth weight
- climate change
- blood brain barrier
- dengue virus