Abstract
Immune surveillance of the CNS is critical for preventing infections; however, there is no accepted experimental model to assess the risk of infection when utilizing disease-modifying agents. We tested two approved agents for patients with multiple sclerosis (MS), glatiramer acetate and fingolimod, in an experimental model of CNS immune surveillance. C57BL/6 mice were infected with the ME49 strain of the neuroinvasive parasite Toxoplasma gondii (T. gondii) and then treated with GA and fingolimod. Neither treatment affected host survival; however, differences were observed in parasite load and in leukocyte numbers in the brains of infected animals. Here we demonstrate that this model could be a useful tool for analyzing immune surveillance.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 232-235 |
| Number of pages | 4 |
| Journal | Journal of Neuroimmunology |
| Volume | 276 |
| Issue number | 1-2 |
| DOIs | |
| State | Published - Nov 15 2014 |
Keywords
- EAE
- Experimental autoimmune encephalomyelitis
- Immune surveillance
- Toxoplasma gondii
ASJC Scopus subject areas
- Immunology and Allergy
- Immunology
- Neurology
- Clinical Neurology