Tolerability and immunogenicity of an intranasally-administered adenovirus-vectored COVID-19 vaccine: An open-label partially-randomised ascending dose phase I trial.


Journal

EBioMedicine
ISSN: 2352-3964
Titre abrégé: EBioMedicine
Pays: Netherlands
ID NLM: 101647039

Informations de publication

Date de publication:
Nov 2022
Historique:
received: 03 05 2022
revised: 08 09 2022
accepted: 16 09 2022
pubmed: 14 10 2022
medline: 16 11 2022
entrez: 13 10 2022
Statut: ppublish

Résumé

Intranasal vaccination may induce protective local and systemic immune responses against respiratory pathogens. A number of intranasal SARS-CoV-2 vaccine candidates have achieved protection in pre-clinical challenge models, including ChAdOx1 nCoV-19 (AZD1222, University of Oxford / AstraZeneca). We performed a single-centre open-label Phase I clinical trial of intranasal vaccination with ChAdOx1 nCoV-19 in healthy adults, using the existing formulation produced for intramuscular administration. Thirty SARS-CoV-2 vaccine-naïve participants were allocated to receive 5 × 10 Reactogenicity was mild or moderate. Antigen-specific mucosal antibody responses to intranasal vaccination were detectable in a minority of participants, rarely exceeding levels seen after SARS-CoV-2 infection. Systemic responses to intranasal vaccination were typically weaker than after intramuscular vaccination with ChAdOx1 nCoV-19. Antigen-specific mucosal antibody was detectable in participants who received an intramuscular mRNA vaccine after intranasal vaccination. Seven participants developed symptomatic SARS-CoV-2 infection. This formulation of intranasal ChAdOx1 nCoV-19 showed an acceptable tolerability profile but induced neither a consistent mucosal antibody response nor a strong systemic response. AstraZeneca.

Sections du résumé

BACKGROUND BACKGROUND
Intranasal vaccination may induce protective local and systemic immune responses against respiratory pathogens. A number of intranasal SARS-CoV-2 vaccine candidates have achieved protection in pre-clinical challenge models, including ChAdOx1 nCoV-19 (AZD1222, University of Oxford / AstraZeneca).
METHODS METHODS
We performed a single-centre open-label Phase I clinical trial of intranasal vaccination with ChAdOx1 nCoV-19 in healthy adults, using the existing formulation produced for intramuscular administration. Thirty SARS-CoV-2 vaccine-naïve participants were allocated to receive 5 × 10
FINDINGS RESULTS
Reactogenicity was mild or moderate. Antigen-specific mucosal antibody responses to intranasal vaccination were detectable in a minority of participants, rarely exceeding levels seen after SARS-CoV-2 infection. Systemic responses to intranasal vaccination were typically weaker than after intramuscular vaccination with ChAdOx1 nCoV-19. Antigen-specific mucosal antibody was detectable in participants who received an intramuscular mRNA vaccine after intranasal vaccination. Seven participants developed symptomatic SARS-CoV-2 infection.
INTERPRETATION CONCLUSIONS
This formulation of intranasal ChAdOx1 nCoV-19 showed an acceptable tolerability profile but induced neither a consistent mucosal antibody response nor a strong systemic response.
FUNDING BACKGROUND
AstraZeneca.

Identifiants

pubmed: 36229342
pii: S2352-3964(22)00480-7
doi: 10.1016/j.ebiom.2022.104298
pmc: PMC9550199
pii:
doi:

Substances chimiques

Antibodies, Viral 0
BNT162 Vaccine 0
ChAdOx1 nCoV-19 B5S3K2V0G8
COVID-19 Vaccines 0
Viral Vaccines 0

Types de publication

Clinical Trial, Phase I Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

104298

Informations de copyright

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

Déclaration de conflit d'intérêts

Declaration of interests Oxford University has entered into a partnership with AstraZeneca to develop ChAdOx1 nCoV-19. AJR and KE may receive royalties arising from the University of Oxford/AstraZeneca COVID-19 vaccine. TL is named as an inventor on a patent application covering this SARS-CoV-2 vaccine and was previously a consultant to Vaccitech on an unrelated project. AVSH is a cofounder of and former consultant to Vaccitech is named as an inventor on a patent covering design and use of ChAdOx1-vectored vaccines (PCT/GB2012/000467), and may receive royalties arising for the University of Oxford/AstraZeneca COVID-19 vaccine. DW, EJK, TV, and JAG are current employees of AstraZeneca and hold or may hold AstraZeneca stock. ADD reports grants and personal fees from AstraZeneca outside of the submitted work, is a named inventor on patent applications relating the chimpanzee adenovirus platform technology and manufacturing, and may receive royalties arising from the University of Oxford/AstraZeneca COVID-19 vaccine. All other authors declare no competing interests.

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Auteurs

Meera Madhavan (M)

Jenner Institute, University of Oxford, Old Road Campus Research Building, Oxford OX3 7BN, UK; Centre for Clinical Vaccinology and Tropical Medicine, University of Oxford, Churchill Hospital, Oxford OX3 7LE, UK.

Adam J Ritchie (AJ)

Jenner Institute, University of Oxford, Old Road Campus Research Building, Oxford OX3 7BN, UK.

Jeremy Aboagye (J)

Jenner Institute, University of Oxford, Old Road Campus Research Building, Oxford OX3 7BN, UK.

Daniel Jenkin (D)

Jenner Institute, University of Oxford, Old Road Campus Research Building, Oxford OX3 7BN, UK; Centre for Clinical Vaccinology and Tropical Medicine, University of Oxford, Churchill Hospital, Oxford OX3 7LE, UK.

Samuel Provstgaad-Morys (S)

Jenner Institute, University of Oxford, Old Road Campus Research Building, Oxford OX3 7BN, UK.

Iona Tarbet (I)

Jenner Institute, University of Oxford, Old Road Campus Research Building, Oxford OX3 7BN, UK.

Danielle Woods (D)

Jenner Institute, University of Oxford, Old Road Campus Research Building, Oxford OX3 7BN, UK.

Sophie Davies (S)

Jenner Institute, University of Oxford, Old Road Campus Research Building, Oxford OX3 7BN, UK.

Megan Baker (M)

Centre for Clinical Vaccinology and Tropical Medicine, University of Oxford, Churchill Hospital, Oxford OX3 7LE, UK.

Abigail Platt (A)

Centre for Clinical Vaccinology and Tropical Medicine, University of Oxford, Churchill Hospital, Oxford OX3 7LE, UK.

Amy Flaxman (A)

Jenner Institute, University of Oxford, Old Road Campus Research Building, Oxford OX3 7BN, UK.

Holly Smith (H)

Jenner Institute, University of Oxford, Old Road Campus Research Building, Oxford OX3 7BN, UK.

Sandra Belij-Rammerstorfer (S)

Jenner Institute, University of Oxford, Old Road Campus Research Building, Oxford OX3 7BN, UK.

Deidre Wilkins (D)

Translational Medicine, Vaccines & Immune Therapies, BioPharmaceuticals R&D, AstraZeneca, 1 Medimmune Way, Gaithersburg, MD 20878, USA.

Elizabeth J Kelly (EJ)

Translational Medicine, Vaccines & Immune Therapies, BioPharmaceuticals R&D, AstraZeneca, 1 Medimmune Way, Gaithersburg, MD 20878, USA.

Tonya Villafana (T)

Clinical Development, Vaccines & Immune Therapies, BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, MD, USA.

Justin A Green (JA)

Clinical Development, Vaccines & Immune Therapies, BioPharmaceuticals R&D, AstraZeneca, Cambridge, UK.

Ian Poulton (I)

Centre for Clinical Vaccinology and Tropical Medicine, University of Oxford, Churchill Hospital, Oxford OX3 7LE, UK.

Teresa Lambe (T)

Jenner Institute, University of Oxford, Old Road Campus Research Building, Oxford OX3 7BN, UK; Oxford Vaccine Group, Centre for Clinical Vaccinology and Tropical Medicine, University of Oxford, Churchill Hospital, Oxford OX3 7LE, UK; China Academy of Medical Sciences Oxford Institute, University of Oxford, NDM Research Building, Old Road Campus, Headington, Oxford OX3 7FZ, UK.

Adrian V S Hill (AVS)

Jenner Institute, University of Oxford, Old Road Campus Research Building, Oxford OX3 7BN, UK.

Katie J Ewer (KJ)

Jenner Institute, University of Oxford, Old Road Campus Research Building, Oxford OX3 7BN, UK.

Alexander D Douglas (AD)

Jenner Institute, University of Oxford, Old Road Campus Research Building, Oxford OX3 7BN, UK. Electronic address: sandy.douglas@ndm.ox.ac.uk.

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