To obtain a good animal model for polymyositis, we previously induced exper
imental autoimmune myositis (EAM) in Lewis rats by immunization with partia
lly purified skeletal myosin. However, the nature of EAM-inducing antigen(s
) in the partially purified myosin preparation remains unclear because it m
ay contain several myositogenic antigens. In the present study, we further
purified myosin and C-protein from partially purified myosin preparations a
nd examined their EAM-inducing ability. It was revealed that immunization w
ith both C-protein and purified myosin elicited EAM, which was essentially
the same as that induced by partially purified myosin. However, their myosi
togenic ability was quite different. C-protein induced severe EAM of high h
istological grade and lesion frequency, whereas purified myosin induced onl
y mild EAM. Immunohistochemical staining of C-protein-induced lesions demon
strated that muscle fiber-infiltrating cells were CD8 beta(+) T cells and m
acrophages and that CD4(+) cells were mainly located in the endomysium and
interfiber connective tissue. Collectively, these findings suggest that C-p
rotein in the skeletal muscle is the major myositogenic antigen and induces
inflammatory lesions mimicking those of human polymyositis. (C) 1999 Elsev
ier Science B.V. All rights reserved.