The myelin oligodendrocyte glycoprotein (MOG): a model for antibody-mediated demyelination in experimental autoimmune encephalomyelitis and multiple sclerosis
A. Stefferl et al., The myelin oligodendrocyte glycoprotein (MOG): a model for antibody-mediated demyelination in experimental autoimmune encephalomyelitis and multiple sclerosis, J NEUR TR-S, (58), 2000, pp. 123-133
The myelin oligodendrocyte glycoprotein (MOG) is a major target for autoant
ibody mediated demyelination in experimental autoimmune encephalomyelitis (
EAE). In the current review we discuss the epitope specificity of this anti
body response, in particular evidence suggesting that pathogenic anti-MOG a
ntibodies are preferentially directed against conformation-dependent epitop
es present on the extracellular immunoglobulin domain of the protein. Surpr
isingly, recent data suggest that this autoimmune response is in part regul
ated by polymorphisms in the MOG gene itself, an observation that may have
important implications for the genetic and immunological stratification of
patients with multiple sclerosis.