[Vaccination against hepatitis B in children with chronic hematologic diseases treated with immunosuppression]
T Jackowska1, R Rokicka-Milewska, K Madaliński
1Katedra i Klinika Pediatrii, Hematologii i Onkologii Akademii Medycznej w Warszawie.
Insights
Vaccinating children against hepatitis B during early cancer treatment effectively builds immunity. Protective antibody levels persist for six years, but a shortened vaccine schedule proved ineffective for these patients.
Area of Science:
- Immunology
- Pediatric Oncology
- Vaccinology
Background:
- Hepatitis B infection poses risks in managing pediatric cancer and aplastic anemia.
- Effective hepatitis B prevention is crucial for immunocompromised children undergoing cancer therapy.
Purpose of the Study:
- To evaluate the efficacy of active immunization with hepatitis B vaccine (Engerix B) in children with various cancers.
- To determine the duration of protective antibody levels post-vaccination.
- To compare the effectiveness of standard versus shortened vaccination schedules.
Main Methods:
- Children with Hodgkin's disease, solid tumors, and leukemia received hepatitis B vaccination (Engerix B).
- Vaccination timing varied: during early immunosuppressive therapy for solid tumors/Hodgkin's, and post-therapy for leukemia.
- Antibody levels were monitored for seroconversion and long-term protection.
- A subset received a shortened vaccination schedule (0-10-20 days).
Main Results:
- Children with Hodgkin's disease and solid tumors responded well to vaccination during early immunosuppressive therapy.
- Leukemia patients achieved effective immunization after completing immunosuppressive therapy.
- Protective antibody levels were maintained for at least 6 years post-vaccination.
- The shortened vaccination schedule (0-10-20 days) was ineffective in this pediatric cohort.
- Immune disorders were identified as a cause for lack of seroconversion in 6 children.
Conclusions:
- Active immunization with hepatitis B vaccine is effective in pediatric cancer patients, with optimal timing depending on the specific condition and therapy.
- Long-term protection is achievable, highlighting the importance of timely vaccination.
- Standard vaccination schedules are recommended over shortened ones for immunocompromised children.
- Passive immunization is advised for children with chronic neoplastic hematological diseases during immunosuppression.
Abstract:
Prevention of hepatitis B infection is an important factor in the successful management of cancer and aplastic anaemia cases. Our result suggested that children with Hodgkin's disease and solid tumors vaccinated during early stage of immunosuppressive therapy are good responders to hepatitis B vaccine. Active immunisation with hepatitis B vaccine (Engerix B), was also effective in children with leukaemia after completing immunosuppressive therapy. Protective levels of antibodies remained 6 years after vaccination. Vaccination according to shortened schedule (0-10-20 days) was not effective in these children. Passive immunisation is indicated in children with chronic neoplastic haematological diseases during immunosuppressive therapy. In 6 children the lack of seroconversion after vaccination was due to immune disorders.
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