MAJOR HISTOCOMPATIBILITY COMPLEX-CONTROLLED PROTECTIVE INFLUENCES ON EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS ARE PEPTIDE-SPECIFIC

The myelin basic protein (MBP) peptide 63-88-induced experimental auto immune encephalomyelitis (EAE) and its associated T cell cytokine prof ile are influenced by the rat major histocompatibility complex (MHC). There is an allele-specific protective influence of the MHC class I re gion, whereas the MHC class II region display either disease-protectiv e or -promoting effects. To investigate if the MHC-associated protecti on is dependent on certain combinations of MBP peptide and MHC molecul es, we have now used another peptide (MBP 89-101). A broader and diffe rent set of rat MHC alleles were associated with EAE induced with MBP 89-101 as compared to MBP 63-88. All EAE-susceptible strains mounted p eptide-specific strong T helper (Th) 1-like immune responses in vitro. Immunization of rats with an extended peptide (MBP 87-110) induced EA E associated with the same MHC haplotypes as the 89-101 peptide, excep t in LEW.1N (RT1(n)) rats which were relatively resistant. Only this s train responded with additional Th2-like and transforming growth facto r-beta responses to the peptide iii vitro. In vivo depletion of CD8(+) cells aggravated the disease in this strain. We conclude that both MH C-controlled promoting and protective influences on EAE are dependent on certain MHC/MBP peptide combinations, and that the 87-110 region of MBP contains a major MHC-associated encephalitogenic epitope in the r at.