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Response to hepatitis A and B vaccination in pediatric patients with celiac disease
Nafiye Urganci1, Derya Kalyoncu
1Division of Pediatric Gastroenterology, Department of Pediatrics, Sisli Etfal Training and Research Hospital, Istanbul, Turkey.
Insights
Pediatric patients with celiac disease show a reduced response to hepatitis A and B vaccines compared to healthy children. This suggests a need for careful vaccination strategies in this population.
Area of Science:
- Immunology
- Pediatrics
- Gastroenterology
Background:
- Celiac disease (CD) is an autoimmune disorder affecting children.
- Assessing vaccine immunogenicity in pediatric CD patients is crucial for public health.
- Hepatitis A and B are significant viral infections preventable by vaccination.
Purpose of the Study:
- To evaluate the immune response to hepatitis A and B vaccinations in children diagnosed with celiac disease.
- To compare vaccination efficacy in pediatric CD patients versus healthy controls.
Main Methods:
- A cohort of 30 pediatric patients (ages 1-15) with CD was compared to 50 healthy controls.
- Participants received standard hepatitis A and B vaccine regimens.
- Serological testing assessed antibody levels before and after vaccination, including follow-up evaluations.
Main Results:
- Lower seroconversion rates were observed in CD patients for both hepatitis A (75% vs 100%) and hepatitis B (70% vs 90% after primary series).
- A significant difference in seroprotection was noted for hepatitis B vaccine efficacy (P=0.03 after primary, P=0.04 after full series).
- Four CD patients were unresponsive to both vaccines, and antibody levels remained stable during follow-up.
Conclusions:
- Pediatric patients with celiac disease exhibit a diminished seroconversion rate to hepatitis A and B vaccines compared to healthy individuals.
- The findings highlight potential challenges in achieving adequate immunity against hepatitis A and B in this vulnerable population.
- Further research may be warranted to optimize vaccination protocols for children with celiac disease.
Objectives:
The aim of the study was to evaluate the response to hepatitis A and B vaccinations in pediatric patients with celiac disease (CD).
Methods:
Thirty patients with CD ages 1 to 15 years were compared with 50 healthy age-, sex-, and body mass index-matched controls. Screening for hepatitis A and B serology was carried out before vaccination. Susceptible cases received 20 μg of recombinant DNA vaccine for hepatitis B (0,1, and 6 months) and 720 milliELISA units of inactivated hepatitis A virus (HAV) vaccine (0 and 6 months). Postvaccination serologic evaluation was performed 1 month after the last dose of primary vaccination, 1 month after the booster dose, and once every year during follow-up.
Results:
Sixteen patients and 35 controls received hepatitis A vaccine; protective anti-HAV antibodies were developed in 12 (75%) of the patients and all of the controls (75% vs 100%, respectively; 95% confidence interval [CI] 0.47-0.92, P=0.007). Thirty patients and 50 controls received hepatitis B vaccine, and 70% of the patients vs 90% of the controls achieved seroprotection (anti-HBs titers ≥10 mIU/mL) 1 month after primary vaccination (95% CI 0.74-0.90, P=0.03). Four patients were unresponsive to both of the vaccines. The overall seroprotection rates were 96% in controls and 80% in patients after the whole hepatitis B vaccination series (95% CI 0.04-0.18, P=0.04). No significant reduction was observed in antibody response among patients and controls during follow-up period.
Conclusions:
The rate of seroconversion to the hepatitis B virus- and HAV vaccine is lower in patients with CD than in healthy controls.
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