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T Cell Receptor Peptide Therapy Triggers Autoregulation of Experimental Encephalomyelitis

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Encephalitogenic T cells specific for myelin basic protein share common V β 8 peptide sequences in their T cell receptor (TCR) that can induce autoregulatory T cells and antibodies that prevent clinical signs of experimental autoimmune encephalomyelitis (EAE). It is not known, however, if TCR peptides can treat established disease. To test its therapeutic value, TCR-V β 8-39-59 peptide was injected into rats with clinical signs of EAE. This treatment reduced disease severity and speeded recovery, apparently by boosting anti-V β 8 T cells and antibodies raised naturally in response to encephalitogenic V β 8 + T cells. These results demonstrate that synthetic TCR peptides can be used therapeutically, and implicate the TCR-V β 8-39-59 sequence as a natural idiotope involved in EAE recovery. Similarly, human TCR peptides may be effective in enhancing natural regulation of autoreactive T cells that share common V genes.
American Association for the Advancement of Science (AAAS)
Title: T Cell Receptor Peptide Therapy Triggers Autoregulation of Experimental Encephalomyelitis
Description:
Encephalitogenic T cells specific for myelin basic protein share common V β 8 peptide sequences in their T cell receptor (TCR) that can induce autoregulatory T cells and antibodies that prevent clinical signs of experimental autoimmune encephalomyelitis (EAE).
It is not known, however, if TCR peptides can treat established disease.
To test its therapeutic value, TCR-V β 8-39-59 peptide was injected into rats with clinical signs of EAE.
This treatment reduced disease severity and speeded recovery, apparently by boosting anti-V β 8 T cells and antibodies raised naturally in response to encephalitogenic V β 8 + T cells.
These results demonstrate that synthetic TCR peptides can be used therapeutically, and implicate the TCR-V β 8-39-59 sequence as a natural idiotope involved in EAE recovery.
Similarly, human TCR peptides may be effective in enhancing natural regulation of autoreactive T cells that share common V genes.

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