Abstract
A T-cell receptor (TCR) peptide vaccine from the Vβ5.2 sequence expressed in multiple sclerosis (MS) plaques and on myelin basic protein (MBP)-specific T cells boosted peptide-reactive T cells in patients with progressive MS. Vaccine responders had a reduced MBP response and remained clinically stable without side effects during one year of therapy, whereas nonresponders had an increased MBP response and progressed clinically. Peptide-specific T helper 2 cells directly inhibited MBP-specific T helper 1 cells in vitro through the release of interleukin-10, implicating a bystander suppression mechanism that holds promise for treatment of MS and other autoimmune diseases.
Original language | English (US) |
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Pages (from-to) | 1109-1115 |
Number of pages | 7 |
Journal | Nature medicine |
Volume | 2 |
Issue number | 10 |
DOIs | |
State | Published - Oct 1996 |
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)