Regulation of encephalitogenic T cells with recombinant TCR ligands

Gregory G. Burrows, Kirsten L. Adlard, Bruce F. Bebo, Justin W. Chang, Kirill Tenditnyy, Arthur A. Vandenbark, Halina Offner

Research output: Contribution to journalArticlepeer-review

36 Scopus citations


We have previously described recombinant MHC class II β1 and α1 domains loaded with free antigenic peptides with potent inhibitory activity on encephalitogenic T cells. We have now produced single-chain constructs in which the peptide Ag is genetically encoded within the same exon as the linked β1 and α1 domains, overcoming the problem of displacement of peptide Ag from the peptide binding cleft. We here describe clinical effects of recombinant TCR ligands (RTLs) comprised of the rat RT1.B β1α1 domains covalently linked to the 72-89 peptide of guinea pig myelin basic protein (RTL-201), to the corresponding 72-89 peptide from rat myelin basic protein (RTL-200), or to cardiac myosin peptide CM-2 (RTL-203). Only RTL-201 possessed the ability to prevent and treat active or passive experimental autoimmune encephalomyelitis. Amelioration of experimental autoimmune encephalomyelitis was associated with a selective inhibition of proliferation response and cytokine production by Ag-stimulated lymph node T cells and a drastic reduction in the number of encephalitogenic and recruited inflammatory cells infiltrating the CNS. The exquisitely selective inhibition could be observed between molecules that differ by a single methyl group (the single amino acid residue difference between RTL-200 (threonine) and RTL-201 (serine) at position 80 of the myelin basic protein peptide). These novel RTLs provide a platform for developing potent and selective human diagnostic and therapeutic agents for treatment of autoimmune disease.

Original languageEnglish (US)
Pages (from-to)6366-6371
Number of pages6
JournalJournal of Immunology
Issue number12
StatePublished - Jun 15 2000

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology


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