Immunogenicity and protective efficacy of adenoviral and subunit RSV vaccines based on stabilized prefusion F protein in pre-clinical models.


Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
07 02 2022
Historique:
received: 21 08 2021
revised: 29 10 2021
accepted: 16 12 2021
pubmed: 3 1 2022
medline: 11 3 2022
entrez: 2 1 2022
Statut: ppublish

Résumé

Respiratory Syncytial Virus (RSV) remains a leading cause of severe respiratory disease for which no licensed vaccine is available. We have previously described the derivation of an RSV Fusion protein (F) stabilized in its prefusion conformation (preF) as vaccine immunogen and demonstrated superior immunogenicity in naive mice of preF versus wild type RSV F protein, both as protein and when expressed from an Ad26 vaccine vector. Here we address the question if there are qualitative differences between the two vaccine platforms for induction of protective immunity. In naïve mice, both Ad26.RSV.preF and preF protein induced humoral responses, whereas cellular responses were only elicited by Ad26.RSV.preF. In RSV pre-exposed mice, a single dose of either vaccine induced cellular responses and strong humoral responses. Ad26-induced RSV-specific cellular immune responses were detected systemically and locally in the lungs. Both vaccines showed protective efficacy in the cotton rat model, but Ad26.RSV.preF conferred protection at lower virus neutralizing titers in comparison to RSV preF protein. Factors that may contribute to the protective capacity of Ad26.RSV.preF elicited immunity are the induced IgG2a antibodies that are able to engage Fcγ receptors mediating Antibody Dependent Cellular Cytotoxicity (ADCC), and the induction of systemic and lung resident RSV specific CD8 + T cells. These data demonstrate qualitative improvement of immune responses elicited by an adenoviral vector based vaccine encoding the RSV preF antigen compared to the subunit vaccine in small animal models which may inform RSV vaccine development.

Identifiants

pubmed: 34973849
pii: S0264-410X(21)01651-0
doi: 10.1016/j.vaccine.2021.12.043
pii:
doi:

Substances chimiques

Antibodies, Neutralizing 0
Antibodies, Viral 0
Respiratory Syncytial Virus Vaccines 0
Viral Fusion Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

934-944

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: [All authors are employees of Janssen Vaccines & Prevention B.V and may be Johnson & Johnson stockholders].

Auteurs

Eirikur Saeland (E)

Janssen Vaccines & Prevention, Leiden, the Netherlands. Electronic address: esaeland@its.jnj.com.

Leslie van der Fits (L)

Janssen Vaccines & Prevention, Leiden, the Netherlands.

Renske Bolder (R)

Janssen Vaccines & Prevention, Leiden, the Netherlands.

Marjolein Heemskerk-van der Meer (M)

Janssen Vaccines & Prevention, Leiden, the Netherlands.

Joke Drijver (J)

Janssen Vaccines & Prevention, Leiden, the Netherlands.

Yolinda van Polanen (Y)

Janssen Vaccines & Prevention, Leiden, the Netherlands.

Cornelis Vaneman (C)

Janssen Vaccines & Prevention, Leiden, the Netherlands.

Lisanne Tettero (L)

Janssen Vaccines & Prevention, Leiden, the Netherlands.

Jan Serroyen (J)

Janssen Vaccines & Prevention, Leiden, the Netherlands.

Hanneke Schuitemaker (H)

Janssen Vaccines & Prevention, Leiden, the Netherlands.

Benoit Callendret (B)

Janssen Vaccines & Prevention, Leiden, the Netherlands.

Johannes P M Langedijk (JPM)

Janssen Vaccines & Prevention, Leiden, the Netherlands.

Roland C Zahn (RC)

Janssen Vaccines & Prevention, Leiden, the Netherlands.

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Classifications MeSH