4.5 Article

Induction of a robust T- and B-cell immune response in non- and low-responders to conventional vaccination against hepatitis B by using a third generation PreS/S vaccine

Journal

VACCINE
Volume 32, Issue 39, Pages 5077-5082

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2014.06.076

Keywords

Hepatitis B Virus; Third generation hepatitis B vaccine; Cellular immune response; Vaccination failure

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Non-responsiveness to conventional hepatitis B vaccines in individuals at high risk of exposure to hepatitis B virus (HBV) is an important public health problem and of particular relevance in health care providers. Yeast-derived conventional HBsAg vaccines fail to induce protective antibody titers in up to 10% of immune competent vaccinees. Therefore, a third generation HBV vaccine, Sci-B-Vac (TM), was developed which contains in addition to the small S antigen the PreS1 and PreS2 antigens. This vaccine proved to induce a highly potent cellular and humoral immune response in healthy individuals as well as protective antibody levels in non- and low-responders to conventional HBV vaccines. The aim of the study was to examine whether Sci-B-Vac (TM) triggers cellular and humoral immunity in individuals who failed immunization with conventional vaccines. We immunized 21 volunteers (15 non- and 6 low-responders) according to the standard vaccination schedule (0, 4 and 24 weeks), determined the cellular immunity by proliferation assay and interferon (IFN)-gamma ELISpot and measured the anti-HBs antibody titers prior to each vaccination and four weeks after the third vaccine dose. Following three vaccinations, PreS/S-specific T-cell proliferation was detected in 8 out of 15 non-responders and 5 out of 6 low-responders. Specific IFN-gamma responses were measured in 2 out of 15 non-responders and 4 out of 6 low-responders. All but one (20/21) study participants developed anti-HBs titers >= 10 IU/I after three vaccinations. Anti-HBs >= 100 IU/L were detected in 12 out of 15 non-responders and in 6 out of 6 low-responders. Anti-HBs >= 10 IU/I and <= 100 IU/I were found in 2 non-responders. These results indicate that Sci-B-Vac (TM) induces cellular immunity as well as protective anti-HBs antibody titers in non- and low-responders. In conclusion, these results confirm that Sci-B-Vac (TM) should be administered to non-responders to conventional HBV vaccines and patients with impaired immune function. (C) 2014 Elsevier Ltd. All rights reserved.

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