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Spontaneous HBsAg loss in Korean patients: relevance of viral genotypes, S gene mutations, and covalently closed circular DNA copy numbers
Article in En | WPRIM | ID: wpr-106801
Responsible library: WPRO
ABSTRACT
BACKGROUND/AIMS: Occult HBV infection can persist following HBsAg loss and be transmitted, but the virological features are not well defined. METHODS: Here we investigated 25 Korean patients who lost HBsAg during follow up, either spontaneously or subsequent to therapy. RESULTS: Whereas subtype adr (genotype C) was found in 96% of HBsAg positive patients, 75 % of patients who lost HBsAg spontaneously were seemed to be infected with the ayw subtype with sequence similar to genotype D. Mutations in the major hydrophilic region (MHR) of HBsAg were found in 7 patients who lost HBsAg spontaneously. The mutations include T123S, M125I/N, C139R, D144E, V177A, L192F, and W196L, some of which have not been reported before. Functional analysis via transfection experiments indicate that the C139R and D144E mutations drastically reduced HBsAg antigenicity, while the Y225del mutation found in one interferon-treated patient impaired HBsAg secretion. CONCLUSIONS: Lack of detectable HBsAg in patient serum could be explained by low level of ccc DNA in liver tissue, low antigenicity of the surface protein, or its secretion defect.
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Full text: 1 Index: WPRIM Main subject: Antiviral Agents / Remission, Spontaneous / DNA, Circular / Molecular Sequence Data / Serotyping / Hepatitis B virus / Amino Acid Sequence / Hep G2 Cells / Republic of Korea / Genotype Limits: Adult / Aged / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Clinical and Molecular Hepatology Year: 2014 Type: Article
Full text: 1 Index: WPRIM Main subject: Antiviral Agents / Remission, Spontaneous / DNA, Circular / Molecular Sequence Data / Serotyping / Hepatitis B virus / Amino Acid Sequence / Hep G2 Cells / Republic of Korea / Genotype Limits: Adult / Aged / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Clinical and Molecular Hepatology Year: 2014 Type: Article