WebB cell antigen presentation is sufficient to drive neuro-inflammation in an animal model of multiple sclerosis. B cell antigen presentation is sufficient to drive neuro-inflammation in an animal model of multiple sclerosis. Michiko Shimoda. 2014, Journal of Neuroimmunology. WebHowever, B cells are known to be critical for disease development in the MOG 1-125-induced EAE model in C57BL/6 mice. As with MS in human patients, EAE is characterized by paralysis caused by CNS …
Experimental autoimmune encephalomyelitis induction in …
WebMOG, are pathogenic and cause EAE upon trans - fer to recipient mice. B-cell-independent EAE, in contrast, cannot be generated with human MOG in these mice, because the encephalitogenic T-cell response is dependent on a serine at position 42, where human MOG comprises a proline [Oliver et al. 2003]. Substituting proline with serine in human … WebSep 11, 2024 · MOG-induced EAE models are divided into B-cell-dependent disease, induced by the recombinant protein MOG 1-117 (rMOG), and B-cell-independent disease, induced by the peptide MOG … porthole style mirror
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WebWe finally evaluated B cell activities in MOG-induced EAE in LEW.1AV1 rats. At various time points, sera were taken and the titres of anti-MOG and anti-MBP antibodies were … WebEAE induction in single gene-deleted mice. Taken together, clinical stages of MOG 35–55-induced EAE in C57BL/6 mice can be separated into two phases: (i) an NR4A2-dependent early/acute phase; and (ii) an NR4A2-independent late/chronic phase (Fig. 1). Eomesodermin-positive helper T cells as a deteriorating component for late/chronic EAE WebJul 3, 2013 · The experimental autoimmune encephalitis (EAE) model is used for preclinical research into the pathogenesis of multiple sclerosis (MS), mostly in inbred, specific pathogen free (SPF)-raised laboratory mice. However, the naive state of the laboratory mouse immune system is considered a major hurdle in the translation of principles from … porthole tv