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Experimental and molecular predictions of the adjuvanticity of snail mucin on hepatitis B vaccine in albino mice

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) f...

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Autores principales: Joshua, Parker Elijah, Nwauzor, Cynthia Ogochukwu, Odimegwu, Damian Chukwu, Ukachukwu, Uzochukwu Gospel, Asomadu, Rita Onyekachukwu, Ezeorba, Timothy Prince Chidike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301616/
https://www.ncbi.nlm.nih.gov/pubmed/34297725
http://dx.doi.org/10.1371/journal.pone.0246915
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author Joshua, Parker Elijah
Nwauzor, Cynthia Ogochukwu
Odimegwu, Damian Chukwu
Ukachukwu, Uzochukwu Gospel
Asomadu, Rita Onyekachukwu
Ezeorba, Timothy Prince Chidike
author_facet Joshua, Parker Elijah
Nwauzor, Cynthia Ogochukwu
Odimegwu, Damian Chukwu
Ukachukwu, Uzochukwu Gospel
Asomadu, Rita Onyekachukwu
Ezeorba, Timothy Prince Chidike
author_sort Joshua, Parker Elijah
collection PubMed
description 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.
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spelling pubmed-83016162021-07-31 Experimental and molecular predictions of the adjuvanticity of snail mucin on hepatitis B vaccine in albino mice Joshua, Parker Elijah Nwauzor, Cynthia Ogochukwu Odimegwu, Damian Chukwu Ukachukwu, Uzochukwu Gospel Asomadu, Rita Onyekachukwu Ezeorba, Timothy Prince Chidike PLoS One Research Article 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. Public Library of Science 2021-07-23 /pmc/articles/PMC8301616/ /pubmed/34297725 http://dx.doi.org/10.1371/journal.pone.0246915 Text en © 2021 Joshua et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Joshua, Parker Elijah
Nwauzor, Cynthia Ogochukwu
Odimegwu, Damian Chukwu
Ukachukwu, Uzochukwu Gospel
Asomadu, Rita Onyekachukwu
Ezeorba, Timothy Prince Chidike
Experimental and molecular predictions of the adjuvanticity of snail mucin on hepatitis B vaccine in albino mice
title Experimental and molecular predictions of the adjuvanticity of snail mucin on hepatitis B vaccine in albino mice
title_full Experimental and molecular predictions of the adjuvanticity of snail mucin on hepatitis B vaccine in albino mice
title_fullStr Experimental and molecular predictions of the adjuvanticity of snail mucin on hepatitis B vaccine in albino mice
title_full_unstemmed Experimental and molecular predictions of the adjuvanticity of snail mucin on hepatitis B vaccine in albino mice
title_short Experimental and molecular predictions of the adjuvanticity of snail mucin on hepatitis B vaccine in albino mice
title_sort experimental and molecular predictions of the adjuvanticity of snail mucin on hepatitis b vaccine in albino mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301616/
https://www.ncbi.nlm.nih.gov/pubmed/34297725
http://dx.doi.org/10.1371/journal.pone.0246915
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