From an in vivo to an in vitro relative potency (IVRP) assay to fully characterize a multicomponent O-antigen based vaccine against Shigella.

Generalized Modules for Membrane Antigens (GMMA) O-antigen Outer membrane vesicles (OMV) Potency assay Shigella

Journal

Carbohydrate polymers
ISSN: 1879-1344
Titre abrégé: Carbohydr Polym
Pays: England
ID NLM: 8307156

Informations de publication

Date de publication:
15 Aug 2023
Historique:
received: 23 12 2022
revised: 16 03 2023
accepted: 12 04 2023
medline: 15 5 2023
pubmed: 13 5 2023
entrez: 12 5 2023
Statut: ppublish

Résumé

Outer membrane vesicles (OMV) represent an innovative platform for the design of polysaccharide based vaccines. Generalized Modules for Membrane Antigens (GMMA), OMV released from engineered Gram-negative bacteria, have been proposed for the delivery of the O-Antigen, key target for protective immunity against several pathogens including Shigella. altSonflex1-2-3 is a GMMA based vaccine, including S. sonnei and S. flexneri 1b, 2a and 3a O-Antigens, with the aim to elicit broad protection against the most prevalent Shigella serotypes, especially affecting children in low-middle income countries. Here we developed an In Vitro Relative Potency assay, based on recognition of O-Antigen by functional monoclonal antibodies selected to bind the key epitopes of the different O-Antigen active ingredients, directly applied to our Alhydrogel-formulated vaccine. Heat-stressed altSonflex1-2-3 formulations were generated and extensively characterized. The impact of detected biochemical changes in in vivo and in vitro potency assays was assessed. The overall results showed how the in vitro assay can replace the use of animals, overcoming the inherently high variability of in vivo potency studies. The entire panel of physico-chemical methods developed will contribute to detect suboptimal batches and will be valuable to perform stability studies. The work on Shigella vaccine candidate can be easily extended to other O-Antigen based vaccines.

Identifiants

pubmed: 37173008
pii: S0144-8617(23)00385-5
doi: 10.1016/j.carbpol.2023.120920
pii:
doi:

Substances chimiques

O Antigens 0
glyceryl methyl methacrylate 0
Shigella Vaccines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

120920

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest All authors are employees of GSK group of Companies. Francesca Micoli and Omar Rossi report ownership of GSK shares.

Auteurs

Francesca Necchi (F)

GSK Vaccines Institute for Global Health (GVGH), Via Fiorentina 1, 53100 Siena, Italy. Electronic address: francesca.x.necchi@gsk.com.

Carlo Giannelli (C)

GSK Vaccines Institute for Global Health (GVGH), Via Fiorentina 1, 53100 Siena, Italy. Electronic address: carlo.x.giannelli@gsk.com.

Alessandra Acquaviva (A)

GSK Vaccines Institute for Global Health (GVGH), Via Fiorentina 1, 53100 Siena, Italy. Electronic address: alessandra.x.acquaviva@gsk.com.

Renzo Alfini (R)

GSK Vaccines Institute for Global Health (GVGH), Via Fiorentina 1, 53100 Siena, Italy. Electronic address: renzo.x.alfini@gsk.com.

Valentina Monaci (V)

GSK Vaccines Institute for Global Health (GVGH), Via Fiorentina 1, 53100 Siena, Italy. Electronic address: valentina.x.monaci@gsk.com.

Vanessa Arato (V)

GSK Vaccines Institute for Global Health (GVGH), Via Fiorentina 1, 53100 Siena, Italy. Electronic address: vanessa.x.arato@gsk.com.

Omar Rossi (O)

GSK Vaccines Institute for Global Health (GVGH), Via Fiorentina 1, 53100 Siena, Italy. Electronic address: omar.x.rossi@gsk.com.

Francesca Micoli (F)

GSK Vaccines Institute for Global Health (GVGH), Via Fiorentina 1, 53100 Siena, Italy. Electronic address: francesca.x.micoli@gsk.com.

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Classifications MeSH