Abstract

Although aluminum-containing adjuvants are widely used in human vaccination due to their excellent safety profile, they exhibit low effectiveness with many recombinant antigens. This study investigated the adjuvanticity of snail mucin with recombinant Hepatitis B Vaccine (rHBsAg). Twenty-five (25) female mice distributed unbiasedly into 5 groups were used in the study and were administered different rHBsAg/Mucin formulation at 7 days intervals. Blood samples were collected a day following the administration for analysis. The results of liver function and body weight analysis were indications that snail mucin had no adverse effect on the mice. The treatment group (administer mucin and rHBsAg) showed significantly (P<0.05) higher mean titres of anti-HBsAg antibodies when compared with the negative controls and the positive control administered with two doses of rHBsAg after the boost doses (day 28). Furthermore, a comparable immune response to positive control administered with three doses rHBaAG was recorded. In silico prediction, studies of the protein-protein interaction of a homology modelled snail mucus protein and HBsAg gave an indication of enhanced HBV antigen-antibody interaction. Therefore, this study has shown that snail mucin possesses some adjuvant properties and enhances immune response towards rHBsAg vaccine. However, there is a need for further molecular dynamics studies to understand its mechanism of action.

Highlights

  • Hepatitis B Virus (HBV) is a causative agent of hepatitis B infection, Approximately, a million people die annually from HBV-related chronic liver diseases, such as liver failure, liver cirrhosis and hepatocellular carcinoma (HCC) [1]

  • Snail mucin-adjuvanted recombinant hepatitis B surface antigen (rHBsAg) vaccine had no adverse effects on experimental mice

  • To investigate if Snail Mucin as an adjuvant could pose some adverse effects on the animals, the body weight of the mice was measured throughout the study

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Summary

Introduction

Hepatitis B Virus (HBV) is a causative agent of hepatitis B infection, Approximately, a million people die annually from HBV-related chronic liver diseases, such as liver failure, liver cirrhosis and hepatocellular carcinoma (HCC) [1]. The disease is majorly transmitted across human population through unprotected sex, birth transmission, transfusion of contaminated blood, and the use of object that are contaminated [2].

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