Abstract
Previous studies of experimental allergic encephalomyelitis (EAE) in the LER rat have suggested that amino acid differences present in the LER TCR V beta 8.2 chain may be associated with disease resistance. We report here that LEW rats bred to express a V beta 8.2 gene from DA rats, identical to that found in LER, are susceptible to EAE induction. Furthermore, T cells infiltrating the spinal cord of diseased animals primarily utilized V beta 8.2 and the associated AspSer CDR3 motif, typical of TCR V beta 8.2 chains expressed by pathogenic, anti-MBP responsive T cells in the LEW rat.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Alleles
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Animals
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Encephalomyelitis, Autoimmune, Experimental / genetics*
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Encephalomyelitis, Autoimmune, Experimental / metabolism
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Gene Rearrangement, beta-Chain T-Cell Antigen Receptor
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Genetic Predisposition to Disease
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Haplotypes
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Heterozygote
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Homozygote
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Lymph Nodes / immunology*
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Male
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Polymorphism, Genetic*
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Rats
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Rats, Inbred Lew
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Rats, Inbred Strains
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Receptors, Antigen, T-Cell, alpha-beta / chemistry
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Receptors, Antigen, T-Cell, alpha-beta / genetics*
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Spinal Cord / immunology
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T-Lymphocytes / immunology*
Substances
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Receptors, Antigen, T-Cell, alpha-beta