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Published on: February 1, 2017
Perinatal hepatitis B prevention program in Shandong Province, China. Evaluation and progress
Li Zhang1, Stephen Ko, Jingjing Lv
1a Shandong Provincial Key Laboratory of Infectious Disease Control and Prevention; Shandong Center for Disease Control and Prevention ; Jinan , China.
Hepatitis B vaccine (HepB) and immune globulin (HBIG) significantly reduce perinatal hepatitis B virus (HBV) transmission. Implementation in Shandong Province, China, improved maternal screening and HepB birth dose coverage, but HBIG coverage needs enhancement, especially in western regions.
Area of Science:
- Public Health
- Immunology
- Infectious Diseases
Background:
- Hepatitis B virus (HBV) poses a significant risk for perinatal transmission.
- The World Health Organization recommends hepatitis B vaccine (HepB) for all infants within 24 hours of birth.
- Hepatitis B immune globulin (HBIG) alongside HepB enhances protection for infants born to HBsAg-positive mothers.
Purpose of the Study:
- To assess the implementation progress of HepB birth dose and HBIG in Shandong Province, China.
- To evaluate the effectiveness of these interventions in preventing perinatal HBV transmission.
- To identify barriers and areas for improvement in the vaccination program.
Main Methods:
- Utilized hospital-based reporting data from Shandong Province, China.
- Analyzed trends in maternal screening for HBsAg.
- Tracked HepB birth dose coverage (within 24 hours) and HBIG coverage for infants of HBsAg-positive mothers.
Main Results:
- Maternal screening increased from 70.7% to 96.9% (2004-2012).
- HepB birth dose coverage remained high (96.3-97.1%).
- HBIG coverage for at-risk infants increased from 85.0% to 92.1% after July 2011, but remained lower (81.1%) in western Shandong.
Conclusions:
- HepB birth dose and HBIG integration has improved perinatal HBV prevention in Shandong.
- Consistent high coverage of HepB birth dose is achieved.
- Further efforts are needed to improve HBIG coverage, particularly in western Shandong, and address delays in HepB administration.
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