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Diminished Hepatitis B Antibody Response in Pediatrics With Type 1 Diabetes; the Need for Revaccination Protocol: A
Erfanehsadat Shahim1, Rosemina Bahrololoom2, Maryam Ataollahi3
1Department of Pediatrics Nemazee Teaching Hospital, Shiraz University of Medical Sciences Shiraz Iran.
Insights
Children with type 1 diabetes have significantly lower protective antibody levels after Hepatitis B vaccination compared to healthy children. Vaccination timing and diabetes status impact immune response, necessitating careful consideration for these pediatric patients.
Area of Science:
- Pediatric Endocrinology
- Immunology
- Vaccinology
Background:
- Hepatitis B virus (HBV) infection poses chronic risks, including cirrhosis and hepatocellular carcinoma.
- Anti-Hepatitis B surface antibodies (anti-HBs) indicate protective immunity post-vaccination.
- Assessing seroprotection in pediatric patients with type 1 diabetes mellitus (T1DM) is crucial due to long-term health risks.
Purpose of the Study:
- To compare Hepatitis B vaccine-induced seroprotection in children with T1DM versus nondiabetic children.
- To identify factors influencing inadequate antibody titers in pediatric HBV vaccination.
Main Methods:
- A case-control study involving 127 children with T1DM and 124 healthy controls, all fully vaccinated against HBV.
- Exclusion criteria included immunosuppression, incomplete vaccination, or hepatitis history.
- Logistic regression analyzed odds of inadequate antibody titers, controlling for vaccination timing and diabetes status.
Main Results:
- Children with T1DM had a significantly higher non-protection rate (54.3%) compared to nondiabetics (28.2%).
- Inadequate antibody titers were associated with vaccination timing and T1DM status (OR=2.34).
- Sex, glycemic control, and disease duration over one year did not significantly affect antibody titers.
Conclusions:
- Children with T1DM exhibit diminished anti-HBs antibody levels post-HBV vaccination compared to nondiabetic peers.
- Immune response to HBV vaccination is influenced by diabetes status and vaccination timing.
- These factors are critical for evaluating seroprotection in pediatric populations with T1DM.
Background And Aims:
Hepatitis B virus (HBV) infection is a significant chronic infection in pediatric patients. Vaccination induces production of anti-Hepatitis B surface antibodies, which serve as markers of protective immunity. Given the long-term risks of cirrhosis and hepatocellular carcinoma during adulthood, this study aimed to assess and compare seroprotection between children with type 1 diabetes mellitus (T1DM) and nondiabetic participants.
Methods:
In this case-control study, 127 children with T1DM and 124 controls, all in a healthy immune state and fully vaccinated against HBV, were recruited from Shiraz University pediatric endocrinology clinics. Exclusion criteria included immunosuppression, incomplete vaccination, or hepatitis history in the child/family. Ethical approval was obtained from Shiraz University of Medical Sciences. Comparisons of sex, age, antibody titers, and diabetes indices used appropriate inferential tests; odds of inadequate antibody titers were assessed by logistic regression.
Results:
Considering an antibody titer of 10 mIU/mL as adequate, the non-protection rate was 54.3% (95% CI: 45.3%-63.2%) in diabetic individuals and 28.2% (95% CI:20.5%-37.0%) in non-diabetics. In a multivariable model controlling for time from vaccination, time from vaccination (OR = 1.26, 95% CI: 1.06-1.49, p < 0.001), and diabetes status (OR = 2.34, 95% CI: 1.33-4.14, p = 0.002) contributed to inadequate antibody titers. Sex, glycemic control, and disease duration over 1 year had no significant effect.
Conclusion:
Children with type 1 Diabetes Mellitus exhibited lower anti-HBs antibody titers compared to their nondiabetic counterparts, with no association found with sex or glycemic control. The timing of vaccination and diabetes status should be considered when evaluating immune responses to HBV vaccination in children.
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