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filingDate 2002-10-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2007-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5138f4ab2b834365c687f9b6f738877f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7e95c6566675278fdbaca9f11d038f9c
publicationDate 2007-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2462459-C
titleOfInvention Copolymers for suppression of autoimmune diseases, and methods of use
abstract Random three- and four-amino acid copolymers having lengths of 14-,35- and 50-amino acid residues are provided. Fifty-mers of FEAK were effective inhibitors of MBP 85-99 or proteolipid protein (PLP) 40-60-specific HLA-DR-2-restricted T cell clones. These copolymers efficiently suppressed EAE induced in susceptible SJL/J (H-2s) strain of mice with either whole spinal cord homogenate (WSCH) or with the encephalitogenic epitope PLP 139-151. YFAK 50-mer having a molar ratio of about y 0.8:F 0.2 inhibited binding of biotinylated MBP 85-99 epitope to HLA-DR-2 molecules more efficiently than either unlabeled MBP 85-99 or Copaxone®. YFAK and FAK copolymers efficiently suppressed EAE induced in SJL/J (H-2s) mice with the encephalitogenic epitope PLP 139-151. Copolymers YFK, VYAK and tryptophan-containing VWAK were efficacious in alleviating severity and duration of symptoms of EAE induced by MBP 85-99, in a humanized mouse model expressing genes for both an HLA-DR-2 linked to multiple sclerosis (MS) in humans and for a T cell receptor from an MS patient.
priorityDate 2001-10-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 527.