Amelioration of EAE by a cryptic epitope of myelin oligodendrocyte glycoprotein

髓鞘少突胶质细胞糖蛋白的隐蔽表位对实验性自身免疫性脑脊髓炎的缓解作用

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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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