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 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
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. |
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ISSN: | 0165-5728 |
DOI: | 10.1016/j.jneuroim.2016.06.006 |