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Comparative evaluation of a newly developed 13-valent pneumococcal conjugate vaccine in a mouse model

Animal models facilitate evaluation of vaccine efficacy at relatively low cost. This study was a comparative evaluation of the immunogenicity and protective efficacy of a new 13-valent pneumococcal conjugate vaccine (PCV13) with a control vaccine in a mouse model. After vaccination, anti-capsular an...

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Autores principales: Park, Chulmin, Kwon, Eun-Young, Choi, Su-Mi, Cho, Sung-Yeon, Byun, Ji-Hyun, Park, Jung Yeon, Lee, Dong-Gun, Kang, Jin Han, Shin, Jinhwan, Kim, Hun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443391/
https://www.ncbi.nlm.nih.gov/pubmed/27960627
http://dx.doi.org/10.1080/21645515.2016.1261772
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author Park, Chulmin
Kwon, Eun-Young
Choi, Su-Mi
Cho, Sung-Yeon
Byun, Ji-Hyun
Park, Jung Yeon
Lee, Dong-Gun
Kang, Jin Han
Shin, Jinhwan
Kim, Hun
author_facet Park, Chulmin
Kwon, Eun-Young
Choi, Su-Mi
Cho, Sung-Yeon
Byun, Ji-Hyun
Park, Jung Yeon
Lee, Dong-Gun
Kang, Jin Han
Shin, Jinhwan
Kim, Hun
author_sort Park, Chulmin
collection PubMed
description Animal models facilitate evaluation of vaccine efficacy at relatively low cost. This study was a comparative evaluation of the immunogenicity and protective efficacy of a new 13-valent pneumococcal conjugate vaccine (PCV13) with a control vaccine in a mouse model. After vaccination, anti-capsular antibody levels were evaluated by pneumococcal polysaccharide (PnP) enzyme-linked immunosorbent assay (ELISA) and opsonophagocytic killing assay (OPA). Also, mice were challenged intraperitoneally with 100-fold of the 50% lethal dose of Streptococcus pneumoniae. The anti-capsular IgG levels against serotypes 1, 4, 7F, 14, 18C, 19A, and 19F were high (quartile 2 >1,600), while those against the other serotypes were low (Q2 ≤ 800). Also, the OPA titres were similar to those determined by PnP ELISA. Comparative analysis between new PCV13 and control vaccination group in a mouse model exhibited significant differences in serological immunity of a few serotypes and the range of anti-capsular IgG in the population. Challenge of wild-type or neutropenic mice with serotypes 3, 5, 6A, 6B, and 9V showed protective immunity despite of induced relatively low levels of anti-capsular antibodies. With comparison analysis, a mouse model should be adequate for evaluating serological efficacy and difference in the population level as preclinical trial.
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spelling pubmed-54433912017-06-02 Comparative evaluation of a newly developed 13-valent pneumococcal conjugate vaccine in a mouse model Park, Chulmin Kwon, Eun-Young Choi, Su-Mi Cho, Sung-Yeon Byun, Ji-Hyun Park, Jung Yeon Lee, Dong-Gun Kang, Jin Han Shin, Jinhwan Kim, Hun Hum Vaccin Immunother Research Paper Animal models facilitate evaluation of vaccine efficacy at relatively low cost. This study was a comparative evaluation of the immunogenicity and protective efficacy of a new 13-valent pneumococcal conjugate vaccine (PCV13) with a control vaccine in a mouse model. After vaccination, anti-capsular antibody levels were evaluated by pneumococcal polysaccharide (PnP) enzyme-linked immunosorbent assay (ELISA) and opsonophagocytic killing assay (OPA). Also, mice were challenged intraperitoneally with 100-fold of the 50% lethal dose of Streptococcus pneumoniae. The anti-capsular IgG levels against serotypes 1, 4, 7F, 14, 18C, 19A, and 19F were high (quartile 2 >1,600), while those against the other serotypes were low (Q2 ≤ 800). Also, the OPA titres were similar to those determined by PnP ELISA. Comparative analysis between new PCV13 and control vaccination group in a mouse model exhibited significant differences in serological immunity of a few serotypes and the range of anti-capsular IgG in the population. Challenge of wild-type or neutropenic mice with serotypes 3, 5, 6A, 6B, and 9V showed protective immunity despite of induced relatively low levels of anti-capsular antibodies. With comparison analysis, a mouse model should be adequate for evaluating serological efficacy and difference in the population level as preclinical trial. Taylor & Francis 2016-12-14 /pmc/articles/PMC5443391/ /pubmed/27960627 http://dx.doi.org/10.1080/21645515.2016.1261772 Text en © 2017 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Research Paper
Park, Chulmin
Kwon, Eun-Young
Choi, Su-Mi
Cho, Sung-Yeon
Byun, Ji-Hyun
Park, Jung Yeon
Lee, Dong-Gun
Kang, Jin Han
Shin, Jinhwan
Kim, Hun
Comparative evaluation of a newly developed 13-valent pneumococcal conjugate vaccine in a mouse model
title Comparative evaluation of a newly developed 13-valent pneumococcal conjugate vaccine in a mouse model
title_full Comparative evaluation of a newly developed 13-valent pneumococcal conjugate vaccine in a mouse model
title_fullStr Comparative evaluation of a newly developed 13-valent pneumococcal conjugate vaccine in a mouse model
title_full_unstemmed Comparative evaluation of a newly developed 13-valent pneumococcal conjugate vaccine in a mouse model
title_short Comparative evaluation of a newly developed 13-valent pneumococcal conjugate vaccine in a mouse model
title_sort comparative evaluation of a newly developed 13-valent pneumococcal conjugate vaccine in a mouse model
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443391/
https://www.ncbi.nlm.nih.gov/pubmed/27960627
http://dx.doi.org/10.1080/21645515.2016.1261772
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