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Mutation analysis of DC-SIGN promoter in chronic hepatitis B patients.

Authors :
Chen L
Li C
Meng X
Zhu P
Tan D
Source :
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences [Zhong Nan Da Xue Xue Bao Yi Xue Ban] 2011 Nov; Vol. 36 (11), pp. 1052-8.
Publication Year :
2011

Abstract

Objective: To investigate whether there is mutation in DC-SIGN promoter region in patients with chronic hepatitis B (CHB) and healthy persons previously infected with hepatitis B virus (HBV) and to explore the relationship between the mutation in dendritic cell-specific intercellular adhension molecule-3-grabbing nonintegrin (DC-SIGN) promoter region and HBV.<br />Methods: The studied population was composed of two cohorts: 47 CHB patients and 20 healthy persons previously infected with HBV. The mutation in DC-SIGN promoter region was detected with PCR, single-stranded conformational polymorphism and heteroduplex analysis, cloning, sequencing and aligning the published DC-SIGN promoter sequence.<br />Results: The characteristic mutation within DC-SIGN promoter region in HBV infected individuals was observed. In the DC-SIGN promoter region, 4 hot spot mutations located in positions -139, -142, -222, and -336 were observed in the CHB patients, but only 1 spot mutation located in position -139 was observed in the healthy persons previously infected with HBV. The -336C which was absent in the healthy persons previously infected with HBV was shown in 11 CHB patients (23.40%). The -139T was far more frequent in the healthy persons previously infected with HBV (100%) than in the CHB patients (34.04%).<br />Conclusion: In the DC-SIGN promoter region, -336C may be a genetic risk factor for developing CHB, but -139T may be associated with protection against HBV.

Details

Language :
English
ISSN :
1672-7347
Volume :
36
Issue :
11
Database :
MEDLINE
Journal :
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences
Publication Type :
Academic Journal
Accession number :
22169718
Full Text :
https://doi.org/10.3969/j.issn.1672-7347.2011.11.004