共 50 条
Hepatitis B virus large surface protein in serum as a candidate biomarker for evaluating hepatitis B virus infection
被引:11
|作者:
Wang, Nian-Yue
[2
]
Zhang, Dai
[1
]
Zhao, Wei
[2
]
Li, Bo-An
[3
]
Lin, Chang-Qin
[4
]
机构:
[1] Henan Univ Tradit Chinese Med, Affiliated Hosp 1, Dept Clin Lab, Zhengzhou 450000, Henan Province, Peoples R China
[2] Southeast Univ, Affiliated Hosp 2, Dept Clin Lab, Nanjing, Peoples R China
[3] 302 Hosp PLA, Ctr Clin Lab, Beijing, Peoples R China
[4] Beijing Hotgen Biotech Co Ltd, Beijing, Peoples R China
关键词:
Hepatitis B virus;
Large surface protein;
HBV DNA;
Hepatitis B surface antigens;
Chronic hepatitis B;
PRE-S-REGION;
ANTIGEN;
PARTICLES;
REPLICATION;
VARIANTS;
SEQUENCE;
MARKER;
LIVER;
MICE;
DNA;
D O I:
10.1016/j.clinbiochem.2011.07.002
中图分类号:
R446 [实验室诊断];
R-33 [实验医学、医学实验];
学科分类号:
1001 ;
摘要:
Aim: To develop a sandwich enzyme-linked immunosorbent assay (ELISA) for the detection of serum hepatitis B virus large surface protein (HBV-LP), and study the clinical value of HBV-LP. Methods: Serum HBV-LP levels and a panel of other HBV markers were investigated in a large population of patients with chronic HBV. The clinical value of HBV-LP was evaluated by comparing the coincidence of detection of HBV markers and the change of serum HBV-LP level during antiviral therapy. Results: The ELISA was found to be sensitive and specific for the detection of HBV-LP. Serum HBV-LP level was positively correlated with HBV DNA (r=0.743) in HBV patients. Among the five HBV markers tested, HBV-LP displayed the highest coincidence rate (94.7%) with HBV DNA. Conclusions: Serum HBV-LP was strongly correlated with HBV DNA. This ELISA therefore offers a promising approach for the diagnosis and treatment monitoring of HBV patients. (C) 2011 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
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页码:1199 / 1204
页数:6
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