Amelioration of relapsing experimental autoimmune encephalomyelitis with altered myelin basic protein peptides involves different cellular mechanisms

J Neuroimmunol. 1997 Apr;74(1-2):149-58. doi: 10.1016/s0165-5728(96)00220-2.

Abstract

T-cells specific for a region of human myelin basic protein, amino acids 87-99 (hMBP87-99), have been implicated in the development of multiple sclerosis (MS) a demyelinating disease of the central nervous system. Administration of soluble altered peptide ligand (APL), made by substituting native residues with alanine at either positions 91(91K > A or A91) or 97 (97R > A or A97) in the hMBP87-99 peptide, blocked the development of chronic relapsing experimental autoimmune encephalomyelitis (R-EAE), in the SJL mouse. The non-encephalitogenic APL A91, appears to induce cytokine shifts from Th1 to Th2 in the target T-cells, whereas the encephalitogenic superagonist APL A97 causes deletion of the MBP87-99 responsive cells. Thus, single amino acid changes at different positions in the same peptide epitope can lead to APL capable of controlling auto-immune disease by different mechanisms.

MeSH terms

  • Animals
  • Cell Death
  • Cytokines / metabolism
  • Encephalomyelitis, Autoimmune, Experimental / immunology
  • Encephalomyelitis, Autoimmune, Experimental / pathology
  • Encephalomyelitis, Autoimmune, Experimental / physiopathology*
  • Female
  • Ligands
  • Lymphocyte Activation
  • Mice
  • Mice, Inbred Strains
  • Myelin Basic Protein / immunology
  • Myelin Basic Protein / pharmacology*
  • Peptide Fragments / immunology
  • Peptide Fragments / pharmacology*
  • Recurrence
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / metabolism
  • T-Lymphocytes / physiology

Substances

  • Cytokines
  • Ligands
  • Myelin Basic Protein
  • Peptide Fragments