T. Caballero et al., DETECTION OF HEPATITIS-B VIRUS IN THE LIVER BY IN-SITU HYBRIDIZATION (ISH) IN HBSAG SEROPOSITIVE AND SERONEGATIVE PATIENTS, Histology and histopathology, 10(2), 1995, pp. 265-270
The presence of hepatitis B virus (HBV) DNA in the liver of 119 patien
ts was studied to assess the diagnostic value of in situ hybridization
(ISH) and its relationship with viral replication and histological li
ver damage. Liver biopsies of 119 patients (55 hepatitis B surface ant
igen -HBsAg- seropositive and 64 HBsAg seronegative) were studied retr
ospectively. Among the HBsAg seropositive patients, the ISH was positi
ve in 26 cases (47%) and negative in 29 (53%) and the former group had
higher levels of serum transaminases. The hepatocyte number with posi
tivity for HBsAg and hepatitis B core antigen (HBcAg) in the liver wer
e similar in both ISH-positive and -negative patients. The histologica
l activity index (Knodell) was higher in ISH-positive patients (11 vs
7, p<0.001). Six patients out of 12 were positive by PCR. In the HBsAg
seronegative patients, the ISH was negative in 57 cases and positive
in 7. These 7 were positive for anti-HBs (5 cases) and/or anti-HBc (6
cases); 4 were confirmed by PCR. Thus, our data suggest that the ISH t
echnique is useful for detecting viral nucleic acid in the liver, but
that the HBV-DNA cannot always be considered as a replication marker,
because we also show that some HBsAg seronegative patients with chroni
c liver disease do have HBV-DNA in their liver cells.