Intranasal immunization with outer membrane vesicle pertussis vaccine confers broad protection through mucosal IgA and Th17 responses.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
30 04 2020
Historique:
received: 10 01 2020
accepted: 08 04 2020
entrez: 2 5 2020
pubmed: 2 5 2020
medline: 1 12 2020
Statut: epublish

Résumé

A vaccine based on outer membrane vesicles of pertussis (omvPV) is protective in a mouse-challenge model and induces a broad antibody and mixed Th1/Th2/Th17 response against multiple antigens following subcutaneous immunization. However, this route did not result in mucosal immunity and did not prevent nasopharyngeal colonization. In this study, we explored the potential of intranasal immunization with omvPV. Only intranasal immunization induced strong mucosal immune responses that encompasses enhanced pulmonary and nasal IgA antibody levels, mainly directed against Vag8 and LPS. Furthermore, high numbers of IgA- and IgG-producing plasma cells were detected as well as lung-resident IgA memory B-cells. Finally, only intranasal immunization induced pulmonary Th1/Th17-related cytokine responses. The magnitude and type of systemic immunity was comparable between both routes and included high systemic IgG antibody levels, strong IgG-producing plasma cell responses, memory B-cells residing in the spleen and systemic Th1/Th2/Th17-related cytokine responses. Importantly, only intranasal immunization prevented colonization in both the lungs and the nasal cavity. In conclusion, intranasal omvPV immunization induces mucosal IgA and Th17-mediated responses without influencing the systemic immunity profile. These responses resulted in prevention of Bordetella pertussis colonization in the respiratory tract, including the nasal cavity, thereby potentially preventing transmission.

Identifiants

pubmed: 32355188
doi: 10.1038/s41598-020-63998-2
pii: 10.1038/s41598-020-63998-2
pmc: PMC7192948
doi:

Substances chimiques

Antibodies, Bacterial 0
Immunoglobulin A 0
Pertussis Vaccine 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

7396

Références

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Auteurs

René H M Raeven (RHM)

Intravacc (Institute for Translational Vaccinology), Bilthoven, The Netherlands. rene.raeven@intravacc.nl.

Dedeke Rockx-Brouwer (D)

Intravacc (Institute for Translational Vaccinology), Bilthoven, The Netherlands.

Gaurav Kanojia (G)

Intravacc (Institute for Translational Vaccinology), Bilthoven, The Netherlands.

Larissa van der Maas (L)

Intravacc (Institute for Translational Vaccinology), Bilthoven, The Netherlands.

Tim H E Bindels (THE)

Intravacc (Institute for Translational Vaccinology), Bilthoven, The Netherlands.

Rimko Ten Have (R)

Intravacc (Institute for Translational Vaccinology), Bilthoven, The Netherlands.

Elly van Riet (E)

Intravacc (Institute for Translational Vaccinology), Bilthoven, The Netherlands.

Bernard Metz (B)

Intravacc (Institute for Translational Vaccinology), Bilthoven, The Netherlands.

Gideon F A Kersten (GFA)

Intravacc (Institute for Translational Vaccinology), Bilthoven, The Netherlands.
Division of Drug Delivery Technology, Leiden Academic Center for Drug Research, Leiden University, Leiden, The Netherlands.

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