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Updated: Jun 19, 2026

An Optimized Hemagglutination Inhibition (HI) Assay to Quantify Influenza-specific Antibody Titers
Published on: December 1, 2017
Anti-preS responses influence the anti-HBs response in newborns after vaccination with the third generation Sci-B-Vac
Staffan P E Sylvan1, Kazimierz Madalinski, Ulla B Hellström
1Department of Communicable Disease Control and Prevention, Uppsala County Council, Sweden. staffan.sylvan@lul.se
Insights
This study examined antibody responses to hepatitis B vaccine components in newborns. Higher antibody levels to hepatitis B surface antigen (anti-HBs) were observed in infants lacking reactivity to the preS2 (131-140) epitope.
Area of Science:
- Immunology
- Vaccinology
- Hepatitis B Research
Background:
- The preS1 and preS2 regions of the hepatitis B virus (HBV) are crucial for viral entry and immune response.
- Sci-B-Vac is a preS-containing hepatitis B vaccine used for infant immunization.
- Understanding antibody responses to specific preS epitopes is vital for vaccine efficacy assessment.
Purpose of the Study:
- To analyze the antibody response to the preS1 (21-47) and preS2 (131-140) epitopes following Sci-B-Vac vaccination in newborns.
- To determine the relationship between anti-preS1 and anti-preS2 antibody responses and the overall antibody response to hepatitis B surface antigen (anti-HBs).
Main Methods:
- Twenty-eight healthy newborns were vaccinated with three doses of Sci-B-Vac.
- Antibody levels against preS1 (21-47), preS2 (131-140), and HBsAg were measured at 6 and/or 9 months post-vaccination.
- Statistical analysis was performed to compare anti-HBs levels between groups based on preS reactivity.
Main Results:
- 61% of newborns developed detectable anti-preS1 (21-47) antibodies, and 50% were reactive to anti-preS2 (131-140).
- Mean anti-HBs levels were significantly higher in infants non-reactive to preS2 (131-140) compared to those who were reactive (24580 IU/l vs 7287 IU/l).
- The highest anti-HBs levels were observed in infants with anti-preS1 (21-47) reactivity but without anti-preS2 (131-140) reactivity.
Conclusions:
- Antibody responses to preS1 and preS2 epitopes vary among infants vaccinated with Sci-B-Vac.
- Lack of reactivity to the preS2 (131-140) epitope is associated with significantly higher anti-HBs levels.
- These findings highlight the differential impact of preS epitope responses on hepatitis B vaccine immunogenicity.
Abstract:
We analysed the specificity and significance of the antibody response towards the linear preS1 sequence that has been shown to represent the "hepatocyte binding site" comprising amino acids preS1 (21-47) or the specific preS2 (131-140) antibody response to the "polymerised albumin receptor" in relation to the antibody response to hepatitis B surface antigen during immunisation of healthy children with the preS-containing Sci-B-Vac vaccine. Twenty-eight healthy newborns received three doses of the Sci-B-Vac vaccine according to a 0-, 1-, and 6-month scheme. Seventeen (61%) of the 28 newborns had detectable levels of anti-preS1 (21-47) antibodies and 14 (50%) were anti-preS2 (131-140) reactive at 6 and/or 9 months after initiation of the vaccination. The mean levels of anti-HBs were significantly higher in the anti-preS2 (131-140) non-reactive (24580+/-7815IU/l, mean+SEM) compared with the reactive sera (7287+/-2317IU/l, p<0.025). The highest anti-HBs levels were found in newborns who exhibited reactivity towards the aa 21-47 of the preS1 but lacked anti-preS2 (131-140) reactivity.
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