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Updated: Jul 28, 2026

Bioluminescence Imaging to Detect Late Stage Infection of African Trypanosomiasis
Published on: May 18, 2016
Macrophage procoagulant activity in experimental African trypanosomiasis
Infections with Trypanosoma brucei brucei elevate macrophage procoagulant activity (PCA), potentially causing blood coagulation issues. This effect was reversed with therapy, suggesting a link between parasite pathogenicity and PCA levels.
Area of Science:
- Immunology
- Parasitology
- Hematology
Background:
- Peritoneal macrophages play a key role in immune responses.
- Trypanosoma brucei brucei infection in mice leads to significant immunological changes.
- Procoagulant activity (PCA) in macrophages is crucial for hemostasis.
Purpose of the Study:
- To investigate the changes in procoagulant activity (PCA) of peritoneal macrophages during Trypanosoma brucei brucei infection.
- To determine the relationship between parasite pathogenicity and macrophage PCA.
- To explore the mechanism of macrophage activation by trypanosomes.
Main Methods:
- Induction of Trypanosoma brucei brucei and T. musculi infections in mice.
- Measurement of peritoneal macrophage procoagulant activity (PCA).
- Assessment of macrophage lysosomal enzyme secretion.
- In vitro stimulation of macrophages with trypanosomes (intact and decapsidated).
Main Results:
- Macrophage PCA was significantly elevated during T. brucei brucei infection, returning to normal after therapy.
- PCA levels correlated with parasite pathogenicity; non-pathogenic T. musculi caused minimal changes.
- Macrophages became hyperresponsive to zymosan stimulation for PCA but hyporesponsive for lysosomal enzyme secretion.
- Decapsidation of trypanosomes rendered them highly stimulatory for macrophages, suggesting indirect activation.
Conclusions:
- Elevated macrophage PCA during trypanosome infection may contribute to coagulation abnormalities.
- Parasite pathogenicity, rather than mere presence, influences macrophage PCA.
- Trypanosomes may indirectly activate macrophages, possibly via their glycoprotein coat, leading to altered immune cell function.
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