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Low-dose intradermal administration of recombinant hepatitis B vaccine in children: 5-year follow-up study
Z Kurugöl1, S Erensoy, S Akşit
1Department of Pediatrics, Ege University Faculty of Medicine, Izmir, Turkey. kurugol@med.ege.edu.tr
Insights
Low-dose intradermal hepatitis B vaccine provides long-term protection in children. Even after antibody levels decrease, immunologic memory ensures protection against hepatitis B virus infection for at least five years.
Area of Science:
- Immunology
- Vaccinology
- Pediatrics
Background:
- Low-dose intradermal hepatitis B vaccination efficacy is documented.
- Limited data exists on the long-term protection duration of this administration route.
Purpose of the Study:
- To evaluate the 5-year duration of protection after low-dose intradermal hepatitis B vaccination in children.
- To assess immunologic memory and protection against hepatitis B virus infection.
Main Methods:
- Follow-up of 200 healthy children (infants and preschoolers) immunized intradermally with 2 microg recombinant hepatitis B vaccine at 0, 1, and 6 months.
- Measurement of anti-HBs antibody levels and anti-HBc/HBsAg status over 5 years.
- Evaluation of anamnestic response to a booster dose in seronegative children.
Main Results:
- 97% achieved protective anti-HBs levels (>10 mlU/mL) by 8 weeks post-vaccination.
- Anti-HBs geometric mean titre (GMT) decreased over 5 years but remained protective in 87% of children.
- No children became infected with hepatitis B virus (anti-HBc/HBsAg negative).
- Demonstrated persistent immunologic memory with robust anamnestic response to a booster dose.
Conclusions:
- Intradermal administration of 2 microg recombinant hepatitis B vaccine offers sustained, long-term protection against hepatitis B virus in infants and preschool children.
- The vaccine elicits a persistent immunologic memory, ensuring protection even after antibody levels wane.
Abstract:
Several studies have documented the efficacy of low-dose intradermal administration of hepatitis B vaccine. However, little is known about the duration of protection provided by low-dose intradermal administration of hepatitis B vaccine. This study reports results from a 5-year follow up period of 200 healthy children (100 infants and 100 preschool children) immunized intradermally with 2 microg doses of recombinant hepatitis B vaccine (GenHevac B) at months 0,1, and 6. In the 8th week after the third vaccine dose, 97% of the children developed anti-HBs antibodies higher than or equal to 10 mlU ml(-1), and the antiHBs geometric mean titre (GMT) was 676 mlU ml(-1). In month 18 and year 5, the anti-HBs GMT decreased to approximately one-third (220 mlU ml(-1)) and one-tenth (68 mlU ml(-1)) of the initial levels, respectively. However, 87% of the children had protective levels of anti-HBs (> or =10 mlU ml(-1)) after 5 years. Among 156 children followed for 5 years, none became positive for anti-HBc and/or HbsAg. Seven children who were seronegative after 5 years developed anti-HBs antibodies higher than 1000 mlU ml(-1) after an additional 10 microg intramuscular hepatitis B vaccine. Persistent immunologic memory over periods of 5 years or more is evident, the anamnestic antibody response to a booster dose of vaccine, even in these children who have lost antibody. We conclude that intradermal administration of 2 microg recombinant hepatitis B vaccine provides long-term protection against hepatitis B virus in infants and preschool children.
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