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

Vaccine
|June 28, 2001
PubMed

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.

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