Abstract
Trypanosoma congolense causes a syndrome of variable severity in animals in Africa. Cerebral trypanosomiasis is a severe form, but the mechanism underlying this severity remains unknown. We developed a mouse model of acute cerebral trypanosomiasis and characterized the cellular, behavioral and physiological consequences of this infection. We show large parasite sequestration in the brain vasculature for long periods of time (up to 8 hours) and extensive neuropathology that associate with ICAM1-mediated recruitment and accumulation of T cells in the brain parenchyma. Antibody-mediated ICAM1 blocking and lymphocyte absence reduce parasite sequestration in the brain and prevent the onset of cerebral trypanosomiasis. Here, we establish a mouse model of acute cerebral trypanosomiasis and we propose a mechanism whereby parasite sequestration, host ICAM1, and CD4+ T cells play a pivotal role.
| Original language | English |
|---|---|
| Article number | e77440 |
| Journal | eLife |
| Volume | 11 |
| DOIs | |
| Publication status | Published - Jul 2022 |
| Externally published | Yes |
Keywords
- Animal African trypanosomiasis
- Cerebral trypanosomiasis
- Disease severity
- Immunopathology
- Sequestration
- Trypanosoma congolense
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Dive into the research topics of 'Immunopathology and Trypanosoma congolense parasite sequestration cause acute cerebral trypanosomiasis'. Together they form a unique fingerprint.Research output
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Immunopathology and parasite sequestration cause severe cerebral trypanosomiasis in animals
Pereira, S. S., Niz, M. D., Serre, K., Ouarné, M., Franco, C. A. & Figueiredo, L. M., 5 Nov 2021, p. 1-39, 39 p. (Research Square).Research output: Working paper › Preprint
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