A molecular analysis of viral persistence in surface
antigen-negative chronic hepatitis B.
Kato J, Hasegawa K, Torii N, Yamauchi K, Hayashi N.
Department of Medicine, Institute of Gastroenterology, Tokyo Women's Medical
College, Japan.
To identify the mechanisms of viral persistence in patients with chronic
hepatitis B after the acquisition of anti-hepatitis B surface antigen antibodies
(antiHBs), we serially analyzed the nucleotide sequence of the envelope region
in a cohort of infected patients. Four patients with histological diagnoses of
chronic hepatitis B who had at least 5 years of observance by our hospital staff
were studied. All but one showed
normalization of serum alanineaminotransferase
(ALT) concentration after clearance of the hepatitis B surface of antigen
(HBsAg) and the appearance of anti-HBs. Hepatitis B virus (HBV) DNA was still
detectable by polymerase chain reaction (PCR)
amplification assay in serum specimens from two patients, even in the presence
of circulating anti-HBs. The envelope gene was amplified by PCR in serum
samples obtained both before and after seroconversion, and direct cycle
sequencing of the PCR products was performed. A mutation resulting in a
premature stop codon was found in the pre-S1 region of one patient just prior to
clearance of HBsAg. Two years later, the stop codon was converted to a leucine
codon and three mutations developed in the "a" loop. In the other patient, 16
amino acids had been deleted between amino acids 8 and 23 in the pre-S2 region
before clearance of HBsAg. After the appearance of circulating anti-HBs, the
pre-S2 gene reverted to the wild type but three additional mutations appeared
inside the "a" loop. These results
suggest that HBV mutates when HBsAg is cleared, which may contribute to viral
persistence due to an evasion of the host immune surveillance.