1. Pathology of livers infected with "silent" hepatitis B virus mutant.
- Author
-
Uchida T, Shimojima S, Gotoh K, Shikata T, and Mima S
- Subjects
- Acute Disease, Adult, Aged, Aged, 80 and over, Base Sequence genetics, Biopsy, Needle, Female, Hepatitis B Core Antigens analysis, Hepatitis B Surface Antigens analysis, Humans, Immunoenzyme Techniques, Male, Middle Aged, Molecular Sequence Data, Open Reading Frames genetics, Polymerase Chain Reaction, DNA, Viral analysis, Hepatitis B pathology, Hepatitis B virology, Hepatitis B virus genetics, Hepatitis, Chronic pathology, Hepatitis, Chronic virology, Hepatitis, Viral, Human pathology, Hepatitis, Viral, Human virology, Liver pathology, Liver virology, Point Mutation genetics, Sequence Deletion genetics
- Abstract
We have discovered that non-A, non-B, non-C, non-D, non-E (so-called type F) acute and chronic hepatitis is caused by a hepatitis B virus (HBV) variant with mutations in the X open reading frame. This silent HBV mutant does not induce immunoserological markers. In the present investigation we attempted to elucidate the putative mechanism of hepatocellular necrosis and expression patterns of hepatitis B surface antigen (HBsAg) and core antigen (HBcAg) in biopsied liver tissue. The subjects consisted of 14 patients with acute hepatitis, 11 with chronic hepatitis and eight with liver cirrhosis, all of whom had been previously diagnosed as having so-called hepatitis F. Nine of the 14, 10 of the 11 and all eight, respectively, of the above patients exhibited significant positive immunostaining for HBsAg within their hepatocellular cytoplasm, diffusely or focally. HBcAg stained in a few hepatocellular nuclei in 24.2% of the patients. Histological features were characterized by necroinflammation, indicating immune-mediated hepatocellular necrosis. Despite the serological-marker negativity, the results of immunostaining for HBsAg and HBcAg support replication and expression of HBV DNA, though weak.
- Published
- 1994
- Full Text
- View/download PDF