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

  • Chulmin Park
  • , Eun Young Kwon
  • , Su Mi Choi
  • , Sung Yeon Cho
  • , Ji Hyun Byun
  • , Jung Yeon Park
  • , Dong Gun Lee
  • , Jin Han Kang
  • , Jinhwan Shin
  • , Hun Kim

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)1169-1176
Number of pages8
JournalHuman Vaccines and Immunotherapeutics
Volume13
Issue number5
DOIs
StatePublished - 4 May 2017

Bibliographical note

Publisher Copyright:
© 2017 The Author(s). Published with license by Taylor & Francis © 2017, © Chulmin Park, Eun-Young Kwon, Su-Mi Choi, Sung-Yeon Cho, Ji-Hyun Byun, Jung Yeon Park, Dong-Gun Lee, Jin Han Kang, Jinhwan Shin, and Hun Kim.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Mouse model
  • Neutropenic infection model
  • Streptococcus pneumoniae
  • pneumococcal conjugate vaccine
  • protection efficacy
  • serological evaluation

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