Accumulating evidence indicates that multiple sclerosis, a chronic inf
lammatory disease of the central nervous system, has an autoimmune ori
gin. Since T cells reactive to myelin basic protein (MBP) are thought
to play an important role in the pathogenesis of this disease, it was
assumed that inactivation or depletion of this pathogenic T cell subse
t may have therapeutic effects in multiple sclerosis. We have recently
reported that T cell vaccination, i.e. immunisation with attenuated a
utologous MBP-reactive T cell clones, leads to the depletion of the MB
P-reactive T cells. Furthermore, this approach induced favourable clin
ical effects in the treated patients, encouraging further studies of T
cell vaccination in multiple sclerosis.