Cargando…
Generating enhanced mucosal immunity against Bordetella pertussis: current challenges and new directions
Bordetella pertussis (Bp) is the highly transmissible etiologic agent of pertussis, a severe respiratory disease that causes particularly high morbidity and mortality in infants and young children. Commonly known as “whooping cough,” pertussis is one of the least controlled vaccine-preventable disea...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9990818/ https://www.ncbi.nlm.nih.gov/pubmed/36895562 http://dx.doi.org/10.3389/fimmu.2023.1126107 |
_version_ | 1784902017072758784 |
---|---|
author | Caulfield, Amanda D. Callender, Maiya Harvill, Eric T. |
author_facet | Caulfield, Amanda D. Callender, Maiya Harvill, Eric T. |
author_sort | Caulfield, Amanda D. |
collection | PubMed |
description | Bordetella pertussis (Bp) is the highly transmissible etiologic agent of pertussis, a severe respiratory disease that causes particularly high morbidity and mortality in infants and young children. Commonly known as “whooping cough,” pertussis is one of the least controlled vaccine-preventable diseases worldwide with several countries experiencing recent periods of resurgence despite broad immunization coverage. While current acellular vaccines prevent severe disease in most cases, the immunity they confer wanes rapidly and does not prevent sub clinical infection or transmission of the bacterium to new and vulnerable hosts. The recent resurgence has prompted new efforts to generate robust immunity to Bp in the upper respiratory mucosa, from which colonization and transmission originate. Problematically, these initiatives have been partially hindered by research limitations in both human and animal models as well as potent immunomodulation by Bp. Here, we consider our incomplete understanding of the complex host-pathogen dynamics occurring in the upper airway to propose new directions and methods that may address critical gaps in research. We also consider recent evidence that supports the development of novel vaccines specifically designed to generate robust mucosal immune responses capable of limiting upper respiratory colonization to finally halt the ongoing circulation of Bordetella pertussis. |
format | Online Article Text |
id | pubmed-9990818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99908182023-03-08 Generating enhanced mucosal immunity against Bordetella pertussis: current challenges and new directions Caulfield, Amanda D. Callender, Maiya Harvill, Eric T. Front Immunol Immunology Bordetella pertussis (Bp) is the highly transmissible etiologic agent of pertussis, a severe respiratory disease that causes particularly high morbidity and mortality in infants and young children. Commonly known as “whooping cough,” pertussis is one of the least controlled vaccine-preventable diseases worldwide with several countries experiencing recent periods of resurgence despite broad immunization coverage. While current acellular vaccines prevent severe disease in most cases, the immunity they confer wanes rapidly and does not prevent sub clinical infection or transmission of the bacterium to new and vulnerable hosts. The recent resurgence has prompted new efforts to generate robust immunity to Bp in the upper respiratory mucosa, from which colonization and transmission originate. Problematically, these initiatives have been partially hindered by research limitations in both human and animal models as well as potent immunomodulation by Bp. Here, we consider our incomplete understanding of the complex host-pathogen dynamics occurring in the upper airway to propose new directions and methods that may address critical gaps in research. We also consider recent evidence that supports the development of novel vaccines specifically designed to generate robust mucosal immune responses capable of limiting upper respiratory colonization to finally halt the ongoing circulation of Bordetella pertussis. Frontiers Media S.A. 2023-02-21 /pmc/articles/PMC9990818/ /pubmed/36895562 http://dx.doi.org/10.3389/fimmu.2023.1126107 Text en Copyright © 2023 Caulfield, Callender and Harvill 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 Caulfield, Amanda D. Callender, Maiya Harvill, Eric T. Generating enhanced mucosal immunity against Bordetella pertussis: current challenges and new directions |
title | Generating enhanced mucosal immunity against Bordetella pertussis: current challenges and new directions |
title_full | Generating enhanced mucosal immunity against Bordetella pertussis: current challenges and new directions |
title_fullStr | Generating enhanced mucosal immunity against Bordetella pertussis: current challenges and new directions |
title_full_unstemmed | Generating enhanced mucosal immunity against Bordetella pertussis: current challenges and new directions |
title_short | Generating enhanced mucosal immunity against Bordetella pertussis: current challenges and new directions |
title_sort | generating enhanced mucosal immunity against bordetella pertussis: current challenges and new directions |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9990818/ https://www.ncbi.nlm.nih.gov/pubmed/36895562 http://dx.doi.org/10.3389/fimmu.2023.1126107 |
work_keys_str_mv | AT caulfieldamandad generatingenhancedmucosalimmunityagainstbordetellapertussiscurrentchallengesandnewdirections AT callendermaiya generatingenhancedmucosalimmunityagainstbordetellapertussiscurrentchallengesandnewdirections AT harvillerict generatingenhancedmucosalimmunityagainstbordetellapertussiscurrentchallengesandnewdirections |