@article{22be4d79f464481f80bc12467c1fac85,
title = "T-cell receptor peptide therapy in EAE and MS",
abstract = "Synthetic peptides corresponding to germline TCR Vβ8.2 sequences overexpressed by Lewis rat encephalitogenic T cells are effective in the prevention and treatment of autoimmune encephalomyelitis (EAE). In evaluating optimal conditions for identifying disease-relevant target Vβ genes, we found that the biased expression of Vβ8.2 was most pronounced in the CNS among activated, IL-2 responsive T cells, but was weakly reflected in the cerebrospinal fluid. Evaluation of basic protein reactive T cells from patients with multiple sclerosis revealed biased expression of Vβ5.2 and to a lesser degree, Vβ6.1. Treatment of 11 MS patients with synthetic TCR Vβ5.2 and Vβ6.1 CDR2 peptides boosted the frequency of anti-TCR reactive T cells in a majority of patients, without compromising recall immunity or causing side effects. TCR peptides may be useful in the treatment of human autoimmune diseases, providing that disease-relevant V genes can be identified.",
author = "Vandenbark, \{A. A.\} and Bourdette, \{D. N.\} and R. Whitham and Chou, \{Y. K.\} and Hashim, \{G. A.\} and H. Offner",
year = "1993",
language = "English (US)",
volume = "11",
pages = "S51--S53",
journal = "Clinical and experimental rheumatology",
issn = "0392-856X",
publisher = "Clinical and Experimental Rheumatology S.A.S.",
number = "SUPPL. 8",
}