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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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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. |
format | Online Article Text |
id | pubmed-5443391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
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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