T cell responses to myelin basic protein (MBP) are potentially involved in
the pathogenesis of multiple sclerosis (MS). In this study, we demonstrated
that subcutaneous inoculations with irradiated autologous MBP-reactive T c
ell clones (T cell vaccination) elicited CD8(+) antiidiotypic T cell respon
ses and CD4(+) Th2 cell responses in patients with MS. Both regulatory cell
types induced by T cell vaccination contributed to the inhibition of MBP-r
eactive T cells while they differed in the recognition pattern and function
al properties. We describe for the first time that the Th2 regulatory cells
reacted with activated but not resting T cells in the context of MHC class
II molecules and inhibited the proliferation of MBP-reactive T cells throu
gh the secretion of IL-4 and IL-10. The T-T cell interaction mediated by Th
2 regulatory cells was independent of the antigen specificity of activated
T cells. The findings have important implications for our understanding of
the regulatory mechanism induced by T cell vaccination.