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The role of bactericidal and opsonic activity in immunity against Bordetella pertussis

  • Pascal Blanc*
  • , Yuanqing Liu
  • , Nathalie Reveneau
  • , Breeze Cavell
  • , Andrew Gorringe
  • , Geneviève Renauld-Mongénie
  • *Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

8 Citations (Scopus)

Abstract

Introduction: Pertussis vaccines have drastically reduced the disease burden in humans since their implementation. Despite their success, pertussis remains an important global public health challenge. Bordetella pertussis resurgence could be a result of greater surveillance combined with improved diagnosis methods, changes in Bordetella pertussis biology, vaccine schedules, and/or coverage. Additionally, mechanisms of protection conferred by acellular pertussis (aP) and whole-cell pertussis (wP) vaccines differ qualitatively. There are no clear immune correlates of protection for pertussis vaccines. Pertussis antigens can induce toxin neutralizing antibodies, block adherence or engage complement mediated phagocytic/bactericidal killing. Areas covered: We reviewed the existing evidence on antibody-mediated serum bactericidal and opsonophagocytic activity and discussed the relevance of these functional antibodies in the development of next-generation pertussis vaccines. Expert opinion: Current paradigm proposes that wP vaccines may confer greater herd protection than aP vaccines due to their enhanced clearance of bacteria from the nasopharynx in animal models. Functional antibodies may contribute to the reduction of nasal colonization, which differentiates aP and wP vaccines. Understanding the intrinsic differences in protective immune responses elicited by each class of vaccines will help to identify biomarkers that can be used as immunological end points in clinical trials.

Original languageEnglish
Pages (from-to)1727-1738
Number of pages12
JournalExpert Review of Vaccines
Volume21
Issue number12
DOIs
Publication statusPublished - 2022

Bibliographical note

Funding Information:
This manuscript was funded by Sanofi. We would like to thank Martina Ochs and Denis Macina for their review of the manuscript. We thank Roopsha Brahma, PhD, for manuscript coordination on behalf of Sanofi. Editorial support for this manuscript was provided by Saili Dharadhar (Sanofi).

Publisher Copyright:
© 2022 Sanofi. Published by Informa UK Limited, trading as Taylor & Francis Group.

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

  • Acellular pertussis
  • Whole-cell pertussis
  • bactericidal antibodies
  • mechanism of protection
  • opsonophagocytosis
  • review
  • vaccines

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