Spontaneous HBsAg loss in Korean patients: relevance of viral genotypes, S gene mutations, and covalently closed circular DNA copy numbers.
10.3350/cmh.2014.20.3.251
- Author:
Kyun Hwan KIM
1
;
Hye Young CHANG
;
Jun Yong PARK
;
Eun Sook PARK
;
Yong Kwang PARK
;
Kwang Hyub HAN
;
Sang Hoon AHN
Author Information
1. Department of Pharmacology and Center for Cancer Research and Diagnostic Medicine, IBST, School of Medicine, Konkuk University, Seoul, Korea. khkim10@kku.ac.kr
- Publication Type:Case Reports ; Research Support, Non-U.S. Gov't
- Keywords:
Hepatitis B virus;
HBsAg loss;
ccc DNA;
Mutation
- MeSH:
Adult;
Aged;
Amino Acid Sequence;
Antiviral Agents/therapeutic use;
DNA, Circular/*analysis;
Female;
Genotype;
Hep G2 Cells;
Hepatitis B/drug therapy/*pathology/virology;
Hepatitis B Surface Antigens/blood/*genetics/metabolism;
Hepatitis B virus/genetics/*metabolism;
Humans;
Liver/virology;
Male;
Middle Aged;
Molecular Sequence Data;
Mutation;
Remission, Spontaneous;
Republic of Korea;
Serotyping
- From:Clinical and Molecular Hepatology
2014;20(3):251-260
- CountryRepublic of Korea
- Language:English
-
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.
