Hepatitis B Virus Revaccination With Standard Versus Pre-S Vaccine in Previously Immunized Patients With Celiac Disease

J Pediatr Gastroenterol Nutr. 2015 Oct;61(4):400-3. doi: 10.1097/MPG.0000000000000856.

Abstract

Objective: Previous studies have suggested that hepatitis B virus (HBV) vaccines may be less immunogenic in individuals with celiac disease (CD). A pre-S vaccine (Sci-B-Vac) has demonstrated superior immunogenicity compared with standard HBV vaccines in several diseases. We compared the short-term immunogenicity of a pre-S vaccine with a HBV vaccine (Engerix B) for repeat vaccination of seronegative, previously immunized patients with CD.

Methods: Participants were 1 to 18-year-old children with CD who despite standard HBV vaccines in infancy had nonprotective hepatitis B surface antibody (HBs-Ab) concentrations (≤10 mIU/mL). Patients were randomized to receive either Engerix B or pre-S vaccine. HBs-Ab concentrations were measured 1 month after the first dose. For those who had not responded after 1 dose, measurement was repeated after the third dose.

Results: Children (n = 82) were analyzed (42 pre-S vaccine and 40 Engerix B). Baseline characteristics were similar for both groups, including gluten-free diet status. Both arms showed high response rates following the first injection: 41 (98%) versus 35 (87%) for pre-S vaccine and Engerix B recipients, respectively (P = 0.08). All other patients responded when measured after dose 3. HBs-Ab concentrations (mIU/mL) were higher in the pre-S vaccine group (median 925, interquartile range [IQR] 424-1000) than the Engerix B group (median 363, IQR 106-996, P = 0.005). Twenty (48%) of the pre-S vaccine recipients were "high responders" (>1000 mIU/mL) versus 10 (25%) in Engerix B recipients (P = 0.008).

Conclusions: Both vaccines elicited adequate booster responses in most previously vaccinated patients with CD with nonprotective HBs-Ab concentrations. Pre-S vaccine administration resulted in higher Hbs-Ab concentrations. Our data suggest that a single dose of either vaccine is sufficient to raise titers to protective levels in most patients with CD.

Publication types

  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Academic Medical Centers
  • Adolescent
  • Antibody Formation / drug effects
  • Capsid Proteins / adverse effects
  • Capsid Proteins / genetics
  • Capsid Proteins / metabolism
  • Capsid Proteins / therapeutic use*
  • Celiac Disease / blood
  • Celiac Disease / complications
  • Celiac Disease / immunology*
  • Child
  • Child, Preschool
  • Double-Blind Method
  • Hepatitis B / complications
  • Hepatitis B / immunology
  • Hepatitis B / prevention & control*
  • Hepatitis B Antibodies / analysis*
  • Hepatitis B Surface Antigens / adverse effects
  • Hepatitis B Surface Antigens / genetics
  • Hepatitis B Surface Antigens / metabolism
  • Hepatitis B Surface Antigens / therapeutic use*
  • Hepatitis B Vaccines / adverse effects
  • Hepatitis B Vaccines / genetics
  • Hepatitis B Vaccines / metabolism
  • Hepatitis B Vaccines / therapeutic use*
  • Humans
  • Immunity, Active / drug effects*
  • Immunization, Secondary*
  • Immunocompromised Host / drug effects
  • Infant
  • Israel
  • Lost to Follow-Up
  • Protein Precursors / adverse effects
  • Protein Precursors / genetics
  • Protein Precursors / metabolism
  • Protein Precursors / therapeutic use*
  • Vaccines, Synthetic / adverse effects
  • Vaccines, Synthetic / genetics
  • Vaccines, Synthetic / metabolism
  • Vaccines, Synthetic / therapeutic use

Substances

  • Capsid Proteins
  • Engerix-B
  • Hepatitis B Antibodies
  • Hepatitis B Surface Antigens
  • Hepatitis B Vaccines
  • Pre-S vaccine
  • Protein Precursors
  • Vaccines, Synthetic
  • presurface protein 1, hepatitis B surface antigen
  • presurface protein 2, hepatitis B surface antigen