The immunopathogenesis of autoimmune hepatitis (AIH), and the role of
T cells in the onset and maintenance of this disease, are still unclea
r, Since T cells expand clonally after stimulation by an antigen, it i
s important to analyze the behavior of T cells at a clonal level, We h
ave established recently a novel system, using reverse transcriptase-p
olymerase chain reaction (RTPCR) and subsequent single-strand conforma
tion poly morphism (SSCP) that allows the identification of clonal acc
umulation of T cells in a lymphocyte population, Using this system, we
demonstrated that oligoclonal T cells were accumulated in the liver o
f patients with AIH, and that identical T-cell clonotypes were detecte
d in two different regions of the liver, although these features were
also observed in cases with viral hepatitis. Only in cases with AIH, h
owever, nearly all identical T cells were found to belong to CD8(+) su
bset and there were very few CD4(+) T cells in this population, Our re
sults suggest that common antigens presented to CD8(+) T cells in the
context of HLA class I molecule are distributed diffusely in the liver
of AIH. These findings also suggest that antigens recognized by CD4() T cells may be relatively heterogeneous in the liver with AIH.