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Expression of X protein and hepatitis B virus replication in chronic hepatitis
Author(s) -
Haruna Yoshimichi,
Hayashi Norio,
Katayama Kazuhiro,
Yuki Nobukabu,
Kasahara Akinori,
Sasaki Yutaka,
Fusamoto Hideyuki,
Kamada Takenobu
Publication year - 1991
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.1840130306
Subject(s) - hbcag , hbeag , hbsag , hepatitis b virus , virology , liver biopsy , antigen , hepatitis b , hepatitis b virus dna polymerase , virus , titer , biology , hepatitis , antibody , microbiology and biotechnology , medicine , immunology , biopsy
The X protein can act on the enhancer of hepatitis B virus in an in vitro system and elevate the transcriptional level of hepatitis B virus. However, because no relationship had been reported between X protein expression and hepatitis B virus replication in patients with chronic hepatitis B, we focused on its expression in the liver in comparison with markers of hepatitis B virus replication. Liver biopsy samples and sera from 59 carriers with HBsAg were examined immunohistochemically for X protein using rabbit IgG against recombinant X protein. There was a significant difference in the serum hepatitis B virus DNA level between X protein–positive and –negative patients (p < 0.001). Serum pre‐S1 and pre‐S2 antigens were also measured quantitatively by enzyme immunoassay using monoclonal antibodies specific against each antigen. The titers of pre‐S1 antigen in patients positive for X protein were significantly higher (p < 0.001) than those of the X protein–negative patients (3.02 ± 0.99 vs. 2.00 ± 0.59, respectively). Similarly, the titers of pre‐S2 antigen were 2.98 ± 0.91 vs. 1.94 ± 0.54, respectively (p < 0.001). The rate of positivity of the X protein was higher (38 of 49; 77.6%) in the replicative group (serum HBeAg, serum hepatitis B virus DNA or HBcAg in liver positive) compared with that observed in the nonreplicative group (3 of 10; 30% – serum HBeAg, serum hepatitis B virus DNA and HBcAg in liver negative) (p < 0.01). Our findings indicate that the X protein is closely correlated with hepatitis B virus replication and may have an important role in viral replication in chronic hepatitis B virus infection. (H EPATOLOGY 1991;13:417–421.)