Evaluation of a recombinant DNA hepatitis B vaccine in a vaccinated Nigerian population

Authors

  • Moses P. Adoga Faculty of Natural and Applied Sciences, Nasarawa State University, Keffi, Nigeria.
  • Grace Pennap Faculty of Natural and Applied Sciences, Nasarawa State University, Keffi, Nigeria
  • Becky O. Akande Faculty of Natural and Applied Sciences, Nasarawa State University, Keffi, Nigeria
  • Jamey P. Mairiga Faculty of Natural and Applied Sciences, Nasarawa State University, Keffi, Nigeria
  • Simon Pechulano Innovative Biotech Ltd, Keffi, Nasarawa State, Nigeria.
  • Simon M. Agwale Innovative Biotech USA Inc, Frederick Innovative Technology Center, Frederick Maryland, USA.

DOI:

https://doi.org/10.3855/jidc.823

Keywords:

Shanvac-B, hepatitis B vaccine, HBV, sero-conversion, antibody titre

Abstract

Introduction: Recombinant hepatitis B vaccine was introduced in 1986 and has gradually replaced the plasma-derived hepatitis B vaccine. No published data are available on the immunogenicity of hepatitis B vaccines in Nigerians. The current study aimed to evaluate protective sero-conversion rates after vaccination with Shanvac-B rDNA hepatitis B vaccine in Nigerian subjects between January and September 2009.

Methodology:  After having obtained informed consent and ethical clearance, 2 mL of blood were aseptically collected from each participant aged ≤ 50 years, one month after the first, second and third doses of the vaccine. Sera were separated into cryovials and frozen at -21oC until analysed for the detection of the protective antibody titre induction. Protective antibody titre was defined as a titre of ≥10 mIU/mL.

Results: Of the 376 participants, 192 (51.1%) were males and 184 (48.9%) were females. A total of 144 subjects participated in the first-dose group, nine (6.3%) of whom developed protective antibody titre (8.3% of males and 4.2% of females). Of the 121 participants in the second-dose group, 108 (89.3%) developed protective antibody titre (98.3% of males and 80.3% of females), while of the 111 participants in the third-dose group, 100% protectively sero-converted. Males were more likely to develop protective antibody titre than females after the second dose (P < 0.05).

Conclusion: This data provides additional evidence for the efficacy of Shanvac-B rDNA hepatitis B vaccine and the need to adhere to the recommended three-dose schedule to achieve full and lasting sero-protection among Nigerians.

Author Biographies

Moses P. Adoga, Faculty of Natural and Applied Sciences, Nasarawa State University, Keffi, Nigeria.

Microbiology Unit, Department of Biological Sciences.

 

Lecturer.

Grace Pennap, Faculty of Natural and Applied Sciences, Nasarawa State University, Keffi, Nigeria

Microbiology Unit, Department of Biological Sciences.          

 

Senior Lecturer.

Becky O. Akande, Faculty of Natural and Applied Sciences, Nasarawa State University, Keffi, Nigeria

Graduate

Jamey P. Mairiga, Faculty of Natural and Applied Sciences, Nasarawa State University, Keffi, Nigeria

Department of Biochemistry and Molecular Biology.

Lecturer II. 

Simon Pechulano, Innovative Biotech Ltd, Keffi, Nasarawa State, Nigeria.

Clinical Services Department.

HAART and Site Co-ordinator.

Simon M. Agwale, Innovative Biotech USA Inc, Frederick Innovative Technology Center, Frederick Maryland, USA.

 

Virologist, Vaccinologist, Senior Scientist / CEO.

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Published

2010-08-06

How to Cite

1.
Adoga MP, Pennap G, Akande BO, Mairiga JP, Pechulano S, Agwale SM (2010) Evaluation of a recombinant DNA hepatitis B vaccine in a vaccinated Nigerian population. J Infect Dev Ctries 4:740–744. doi: 10.3855/jidc.823

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Section

Original Articles