Experimental allergic encephalomyelitis (EAE) is an autoimmune demyelinating disease of the central nervous system (CNS) that occurs after immunization of animals with myelin basic protein (MBP). The disease is a prototype model for the study of antigen-specific T helper cell-mediated autoimmune disease. In SJL/J mice, EAE is mediated by T helper cells directed against a 40-amino acid COOH-terminal peptic fragment of mouse small MBP. To identify the minimal T cell epitopes of MBP responsible for EAE, overlapping peptides completely encompassing the epitopes within this region were synthesized. A 28-residue peptide of mouse MBP spanning residues 87-114 (pM87-114) was able to elicit both a strong T cell response and chronic relapsing disease. To better localize the T cell epitopes, shorter peptides within this region were synthesized and two overlapping peptides, pM87-98 and pM91-104, were able to induce EAE. T cell clones and bulk lymph node cell populations reactive with pM87-98 did not respond to pM91-104. However, lymph node cells reactive with pM91-104 also reacted with pM87-98, thus showing that these two peptides represent contiguous, but distinct encephalitogenic epitopes and that both these epitopes may be contained within pM87-98. In addition, pM87-114 and pM87-98 were found to be minor determinants of the total T cell response to rat and rabbit MBP. The restricted response to MBP in SJL/J mice is similar to that of the PL/J mice in that each appears to have only a single peptide region in MBP that elicits encephalitogenic T cells. However, within the region studied, there were two if not more T cell epitopes. This differs from the single encephalitogenic PL/J epitope. These findings of a single encephalitogenic peptide region with multiple T cell epitopes and the fact that encephalitogenic T cell epitopes may be subdominant have implications for the design of treatments directed at the T cell receptor-MHC-peptide epitope complex in autoimmune disease.
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1 July 1988
Article|
July 01 1988
Two minor determinants of myelin basic protein induce experimental allergic encephalomyelitis in SJL/J mice.
D H Kono,
D H Kono
Division of Biology, California Institute of Technology, Pasadena 91125.
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J L Urban,
J L Urban
Division of Biology, California Institute of Technology, Pasadena 91125.
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S J Horvath,
S J Horvath
Division of Biology, California Institute of Technology, Pasadena 91125.
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D G Ando,
D G Ando
Division of Biology, California Institute of Technology, Pasadena 91125.
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R A Saavedra,
R A Saavedra
Division of Biology, California Institute of Technology, Pasadena 91125.
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L Hood
L Hood
Division of Biology, California Institute of Technology, Pasadena 91125.
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D H Kono
,
J L Urban
,
S J Horvath
,
D G Ando
,
R A Saavedra
,
L Hood
Division of Biology, California Institute of Technology, Pasadena 91125.
Online ISSN: 1540-9538
Print ISSN: 0022-1007
J Exp Med (1988) 168 (1): 213–227.
Citation
D H Kono, J L Urban, S J Horvath, D G Ando, R A Saavedra, L Hood; Two minor determinants of myelin basic protein induce experimental allergic encephalomyelitis in SJL/J mice.. J Exp Med 1 July 1988; 168 (1): 213–227. doi: https://doi.org/10.1084/jem.168.1.213
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