A panel of autoantigens (myosin, actin, myelin basic protein MBP, and
thyroglobulin) was used to analyze antigen recognition by the peripher
al blood leukocytes (PBL) of patients with active and stable multiple
sclerosis (MS), patients with other neurological diseases (OND) and he
althy individuals. The immune responsiveness was studied by examining
the in vitro cell proliferation and the increase in the expression of
two T-cell-surface activation markers (the interleukin-2 receptor IL-2
R, and a late activation antigen recognized by the 19.2 monoclonal ant
ibody). In MS, autoantigen recognition occured more frequently than in
the other groups and it was manifested by moderate proliferation or m
arked elevation of the expression of the IL-2R, whereas autoantigen re
cognition in the other groups concerned essentially the expression of
the late activation antigen. Results similar to those described above
were obtained with enriched T lymphocytes either in the presence or ab
sence of IL-2. Our results suggest that the peripheral immune system i
n MS patients may recognize and can be activated by different autoanti
gens and not only by MBP, and that this response is quantitatively and
qualitatively different from that of PBL from OND patients and health
y individuals.