Amelioration of EAE by a c ryptic e pitope of m yelin o ligodendrocyte g lycoprotein

Abstract Previous work demonstrated that EAE induced by recombinant human MOG was B cell-dependent. Data presented here reveal a T cell response to MOG61 – 85 in human rMOG-immunized B cell − / − mice not observed in WT mice. Further study revealed this peptide to be a cryptic epitope in WT mice. Co...

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Veröffentlicht in:Journal of neuroimmunology 2016
Hauptverfasser: Lyons, Jeri A, Riter, Melissa M, Almatrook, Alaa M, Ramsbottom, Michael J, Cross, Anne H
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Sprache:eng
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Zusammenfassung:Abstract Previous work demonstrated that EAE induced by recombinant human MOG was B cell-dependent. Data presented here reveal a T cell response to MOG61 – 85 in human rMOG-immunized B cell − / − mice not observed in WT mice. Further study revealed this peptide to be a cryptic epitope in WT mice. Co-immunization of B cell − / − mice with MOG35 – 55 and MOG61 – 85 peptides led to less severe disease compared to mice immunized with MOG35 – 55 alone. Disease amelioration was associated with decreased production of Interferon-γ by lymph node cells. Thus, MOG61 – 85 represents a protective epitope to human rMOG induced EAE in B cell − / − mice.
ISSN:0165-5728
DOI:10.1016/j.jneuroim.2016.06.006