Selected article for: "clinical course and disease clinical course"

Author: Evonuk, Kirsten S.; Moseley, Carson E.; Doyle, Ryan E.; Weaver, Casey T.; DeSilva, Tara M.
Title: Determining Immune System Suppression versus CNS Protection for Pharmacological Interventions in Autoimmune Demyelination
  • Document date: 2016_9_12
  • ID: vr83284f_15
    Snippet: After induction of EAE in the C57BL/6 mouse model ( Figure 1A , day 0), antigen presentation and proliferation of T cells in the spleen occur on days 1 -5 followed by immune cell infiltration into the CNS around day 7. Approximately 3 to 5 days after the initial immune cell infiltration mice present with clinical scores. To assess if a therapeutic agent is blocking immune cell infiltration into the spinal cord, drugs or vehicle are introduced on .....
    Document: After induction of EAE in the C57BL/6 mouse model ( Figure 1A , day 0), antigen presentation and proliferation of T cells in the spleen occur on days 1 -5 followed by immune cell infiltration into the CNS around day 7. Approximately 3 to 5 days after the initial immune cell infiltration mice present with clinical scores. To assess if a therapeutic agent is blocking immune cell infiltration into the spinal cord, drugs or vehicle are introduced on day 7 after antigen presentation and proliferation in the spleens but before immune cells start to infiltrate into the spinal cord. If immune cell infiltration has been attenuated, the clinical disease course should reflect improved clinical scores during the rising phase of the disease from days 10 to 15 (Figure 2) .

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