Microsomal
antigen autoantibodies are typical of type 2
autoimmune hepatitis, and a strong association with
chronic hepatitis C virus (HCV)
infection has been reported in certain geographical areas. These
autoantibodies have been denominated
LKM-1 to differentiate them from those associated with
thienylic acid-induced
hepatitis (LKM-2) and from those seen in patients with
chronic delta hepatitis (LKM-3). To investigate the
antigenic specificity of
autoantibodies associated with
chronic hepatitis C and delta, we analyzed 52
LKM-1 positive serum samples from patients with
chronic hepatitis C and 17
LKM-3 positive serum samples from patients with
chronic delta hepatitis by indirect immunofluorescence and Western blotting (immunoblotting). Reactivity of subjects with
chronic hepatitis C was heterogeneous: only 5 out of 52
LKM-1 positive patients, tested by Western blot, recognized a single
protein of 50 kD, previously identified by Manns et al. with an immunogenic
epitope of
cytochrome P450IID6. Thirteen of the 52 patients also reacted with a 70 kD microsomal
protein, and 12 out of 52 reacted only with a 59 kD
protein. Twenty-two sera, notwithstanding the high titer in immunofluorescence, did not evidence any reactivity when tested by Western blot. The same sera tested positive in
LKM-1 ELISA when solubilized human microsomal
proteins were used. Fourteen out of 17
LKM-3 positive sera from patients with
chronic hepatitis delta recognized a 55 kD microsomal
protein in Western blot; three sera, HCV and HIV positive, did not react with any
protein by Western blot. None of these sera was positive in ELISA LKM-1.(ABSTRACT TRUNCATED AT 250 WORDS)