| Literature DB >> 25227585 |
Cyd Castro-Rojas1, Krystin Deason1, Rehana Z Hussain1, Liat Hayardeny2, Petra C Cravens1, Felix Yarovinsky3, Todd N Eagar4, Benjamine Arellano1, Olaf Stüve5.
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.Entities:
Keywords: EAE; Experimental autoimmune encephalomyelitis; Immune surveillance; Toxoplasma gondii
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Year: 2014 PMID: 25227585 PMCID: PMC4296723 DOI: 10.1016/j.jneuroim.2014.08.624
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.478