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Potentiating pneumococcal glycoconjugate vaccine PCV13 with saponin adjuvant VSA-1

VSA-1 is a semisynthetic saponin adjuvant prepared from naturally occurring Momordica saponin and capable of stimulating antigen-specific humoral and cellular immune responses. Its immunostimulating activity in enhancing the immune responses induced by the clinical glycoconjugate pneumococcal vaccin...

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Autores principales: Kim, Hyunjung, Yu, Jigui, Bai, Di, Nahm, Moon H., Wang, Pengfei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790987/
https://www.ncbi.nlm.nih.gov/pubmed/36578488
http://dx.doi.org/10.3389/fimmu.2022.1079047
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author Kim, Hyunjung
Yu, Jigui
Bai, Di
Nahm, Moon H.
Wang, Pengfei
author_facet Kim, Hyunjung
Yu, Jigui
Bai, Di
Nahm, Moon H.
Wang, Pengfei
author_sort Kim, Hyunjung
collection PubMed
description VSA-1 is a semisynthetic saponin adjuvant prepared from naturally occurring Momordica saponin and capable of stimulating antigen-specific humoral and cellular immune responses. Its immunostimulating activity in enhancing the immune responses induced by the clinical glycoconjugate pneumococcal vaccine PCV13 is compared with QS-21 in female BALB/c mice. Both VSA-1 and QS-21 boosted IgG and opsonic antibodies titers against seven selected serotypes, including serotypes 3, 14, and 19A that are involved in most PCV13 breakthroughs. Since VSA-1 is much more accessible and of lower toxicity than QS-21, it can be a practical saponin immunostimulant to be included in a new glycoconjugate pneumococcal vaccine formulation.
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spelling pubmed-97909872022-12-27 Potentiating pneumococcal glycoconjugate vaccine PCV13 with saponin adjuvant VSA-1 Kim, Hyunjung Yu, Jigui Bai, Di Nahm, Moon H. Wang, Pengfei Front Immunol Immunology VSA-1 is a semisynthetic saponin adjuvant prepared from naturally occurring Momordica saponin and capable of stimulating antigen-specific humoral and cellular immune responses. Its immunostimulating activity in enhancing the immune responses induced by the clinical glycoconjugate pneumococcal vaccine PCV13 is compared with QS-21 in female BALB/c mice. Both VSA-1 and QS-21 boosted IgG and opsonic antibodies titers against seven selected serotypes, including serotypes 3, 14, and 19A that are involved in most PCV13 breakthroughs. Since VSA-1 is much more accessible and of lower toxicity than QS-21, it can be a practical saponin immunostimulant to be included in a new glycoconjugate pneumococcal vaccine formulation. Frontiers Media S.A. 2022-12-12 /pmc/articles/PMC9790987/ /pubmed/36578488 http://dx.doi.org/10.3389/fimmu.2022.1079047 Text en Copyright © 2022 Kim, Yu, Bai, Nahm and Wang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Kim, Hyunjung
Yu, Jigui
Bai, Di
Nahm, Moon H.
Wang, Pengfei
Potentiating pneumococcal glycoconjugate vaccine PCV13 with saponin adjuvant VSA-1
title Potentiating pneumococcal glycoconjugate vaccine PCV13 with saponin adjuvant VSA-1
title_full Potentiating pneumococcal glycoconjugate vaccine PCV13 with saponin adjuvant VSA-1
title_fullStr Potentiating pneumococcal glycoconjugate vaccine PCV13 with saponin adjuvant VSA-1
title_full_unstemmed Potentiating pneumococcal glycoconjugate vaccine PCV13 with saponin adjuvant VSA-1
title_short Potentiating pneumococcal glycoconjugate vaccine PCV13 with saponin adjuvant VSA-1
title_sort potentiating pneumococcal glycoconjugate vaccine pcv13 with saponin adjuvant vsa-1
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790987/
https://www.ncbi.nlm.nih.gov/pubmed/36578488
http://dx.doi.org/10.3389/fimmu.2022.1079047
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