Exploring the Ability of Meningococcal Vaccines to Elicit Mucosal Immunity: Insights from Humans and Mice

<i>Neisseria meningitidis</i> causes a devastating invasive disease but is also a normal colonizer of the human nasopharynx. Due to the rapid progression of disease, the best tool to protect individuals against meningococcal infections is immunization. Clinical experience with polysaccha...

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Main Authors: Elissa G. Currie, Scott D. Gray-Owen
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:Pathogens
Subjects:
Online Access:https://www.mdpi.com/2076-0817/10/7/906
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spelling doaj-ff132a333d4c4294b92ca5e356e0ea2d2021-07-23T13:59:44ZengMDPI AGPathogens2076-08172021-07-011090690610.3390/pathogens10070906Exploring the Ability of Meningococcal Vaccines to Elicit Mucosal Immunity: Insights from Humans and MiceElissa G. Currie0Scott D. Gray-Owen1Department of Molecular Genetics, Temerty Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A8, CanadaDepartment of Molecular Genetics, Temerty Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada<i>Neisseria meningitidis</i> causes a devastating invasive disease but is also a normal colonizer of the human nasopharynx. Due to the rapid progression of disease, the best tool to protect individuals against meningococcal infections is immunization. Clinical experience with polysaccharide conjugate vaccines has revealed that an ideal meningococcal vaccine must prevent both invasive disease and nasal colonization, which confers herd immunity. However, not all meningococcal vaccines are equal in their ability to prevent nasal colonization, for unknown reasons. Herein, we describe recent efforts to utilize humanized mouse models to understand the impact of different meningococcal vaccines on nasal colonization. These mice are susceptible to nasal colonization, and they become immune following live nasal infection or immunization with matched capsule-conjugate or protein-based vaccines, replicating findings from human work. We bring together insights regarding meningococcal colonization and immunity from clinical work with findings using humanized mouse models, providing new perspective into the different determinants of mucosal versus systemic immunity. Then, we use this as a framework to help focus future studies toward understanding key mechanistic aspects left unresolved, including the bacterial factors required for colonization and immune evasion, determinants of nasal mucosal protection, and characteristics of an ideal meningococcal vaccine.https://www.mdpi.com/2076-0817/10/7/906<i>Neisseria meningitidis</i>meningococcusnasal infectionsepsisvaccinemucosal immunity
collection DOAJ
language English
format Article
sources DOAJ
author Elissa G. Currie
Scott D. Gray-Owen
spellingShingle Elissa G. Currie
Scott D. Gray-Owen
Exploring the Ability of Meningococcal Vaccines to Elicit Mucosal Immunity: Insights from Humans and Mice
Pathogens
<i>Neisseria meningitidis</i>
meningococcus
nasal infection
sepsis
vaccine
mucosal immunity
author_facet Elissa G. Currie
Scott D. Gray-Owen
author_sort Elissa G. Currie
title Exploring the Ability of Meningococcal Vaccines to Elicit Mucosal Immunity: Insights from Humans and Mice
title_short Exploring the Ability of Meningococcal Vaccines to Elicit Mucosal Immunity: Insights from Humans and Mice
title_full Exploring the Ability of Meningococcal Vaccines to Elicit Mucosal Immunity: Insights from Humans and Mice
title_fullStr Exploring the Ability of Meningococcal Vaccines to Elicit Mucosal Immunity: Insights from Humans and Mice
title_full_unstemmed Exploring the Ability of Meningococcal Vaccines to Elicit Mucosal Immunity: Insights from Humans and Mice
title_sort exploring the ability of meningococcal vaccines to elicit mucosal immunity: insights from humans and mice
publisher MDPI AG
series Pathogens
issn 2076-0817
publishDate 2021-07-01
description <i>Neisseria meningitidis</i> causes a devastating invasive disease but is also a normal colonizer of the human nasopharynx. Due to the rapid progression of disease, the best tool to protect individuals against meningococcal infections is immunization. Clinical experience with polysaccharide conjugate vaccines has revealed that an ideal meningococcal vaccine must prevent both invasive disease and nasal colonization, which confers herd immunity. However, not all meningococcal vaccines are equal in their ability to prevent nasal colonization, for unknown reasons. Herein, we describe recent efforts to utilize humanized mouse models to understand the impact of different meningococcal vaccines on nasal colonization. These mice are susceptible to nasal colonization, and they become immune following live nasal infection or immunization with matched capsule-conjugate or protein-based vaccines, replicating findings from human work. We bring together insights regarding meningococcal colonization and immunity from clinical work with findings using humanized mouse models, providing new perspective into the different determinants of mucosal versus systemic immunity. Then, we use this as a framework to help focus future studies toward understanding key mechanistic aspects left unresolved, including the bacterial factors required for colonization and immune evasion, determinants of nasal mucosal protection, and characteristics of an ideal meningococcal vaccine.
topic <i>Neisseria meningitidis</i>
meningococcus
nasal infection
sepsis
vaccine
mucosal immunity
url https://www.mdpi.com/2076-0817/10/7/906
work_keys_str_mv AT elissagcurrie exploringtheabilityofmeningococcalvaccinestoelicitmucosalimmunityinsightsfromhumansandmice
AT scottdgrayowen exploringtheabilityofmeningococcalvaccinestoelicitmucosalimmunityinsightsfromhumansandmice
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