ABSTRACT
The diagnosis of autoimmune hepatitis (AIH) relies on the exclusion of viral, metabolic,
genetic, and toxic etiologies of chronic hepatitis or hepatic injury. There are few
parameters that positively predict the presence of AIH. Autoantibodies have been intensively
evaluated in this respect and have led to the classification of AIH into three serological
subgroups: antinuclear and smooth muscle antibody-positive (ANA/SMA, type 1), liver-kidney
microsomal antibody-positive (LKM-1, type 2), and soluble liver antigen/liver-pancreas
antigen antibody-positive (SLA/LP, type 3) AIH. Although there are few clinical implications
resulting from this classification, autoantibody profiles indicate that AIH is a heterogenous
group of entities. The molecular characterization of B cell autoimmunity has led to
the identification of major phase I and phase II metabolic enzymes as well as structural
and functional components of the cell nucleus as immunologic targets. Autoantibodies
and their corresponding autoantigens are intensively studied to provide clues to the
understanding of disease initiation, tissue specificity, and propagation of hepatic
autoimmune diseases.
KEYWORDS
Autoantibodies - metabolic enzymes - UGT - CYP - LKM - SLA