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Development of a Hepatitis B Virus Reporter System to Monitor the Early Stages of the Replication Cycle
Published on: February 1, 2017
Long-term efficacy of immunization against hepatitis B virus in infants at high-risk analyzed by polymerase chain
1The First Department of Internal Medicine, Nagasaki University School of Medicine, 1-7-1 Sakamoto, Nagasaki, Japan.
Insights
Hepatitis B virus (HBV) immunization effectively protects high-risk infants from perinatal transmission. Most HBV infections occur within the first year, but vaccination provides protection up to 4-6 years of age.
Area of Science:
- Immunology
- Virology
- Pediatrics
Background:
- Perinatal transmission of hepatitis B virus (HBV) is a primary cause of chronic infection.
- Effective immunization strategies are crucial for preventing long-term HBV sequelae in infants.
Purpose of the Study:
- To evaluate the long-term efficacy of hepatitis B immunization in high-risk infants.
- To assess the rate of HBV transmission and viral load using polymerase chain reaction (PCR).
Main Methods:
- A cohort of 251 high-risk infants received hepatitis B immunoglobulin and vaccine between 1981 and 1993.
- Follow-up assessments included HBV-DNA detection via PCR at 1 year and 4-6 years of age.
Main Results:
- HBV-DNA was detected in 36% of infants at 1 year.
- By 4-6 years, the prevalence decreased to 14%, with 2 cases showing breakthrough HBV variants.
- Most HBV infections were identified within the first year of life.
Conclusions:
- Infant immunization against HBV is effective in preventing perinatal transmission up to 4-6 years of age.
- Early detection and intervention are critical, as most infections occur during the first year.
Abstract:
Perinatal transmission of hepatitis B virus (HBV) is a common cause of chronic infection. In the present study, we evaluated the long-term efficacy of immunization against HBV in infants at high-risk, by using polymerase chain reaction (PCR). Two hundred and fifty-one infants received hepatitis B immunoglobulin at birth and a course of hepatitis B vaccine within 6 months of age between 1981 and 1993. Of 251 infants, 203 (81%) and 97 (39%) were followed until 1 and 4-6 years of age, respectively. HBV-DNA was detected by PCR in 74 (36%) of 203 children at 1 year of age, while the prevalence rate of children positive for HBV-DNA decreased to 14 (14%) of 97 children at 4-6 years of age, including 2 children who had the breakthrough variants of HBV. Our results indicate that most of HBV infections occur early, during the first year, and that immunization against HBV effectively protects infants at high-risk against viral transmission, at least up to 4-6 years of age.
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