Serotype 3 Experimental Human Pneumococcal Challenge (EHPC) study protocol: dose ranging and reproducibility in a healthy volunteer population (challenge 3).

Adult thoracic medicine BACTERIOLOGY Clinical Trial Immunology Respiratory infections

Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
10 Jan 2024
Historique:
medline: 11 1 2024
pubmed: 11 1 2024
entrez: 10 1 2024
Statut: epublish

Résumé

Since the introduction of pneumococcal conjugate vaccines, pneumococcal disease rates have declined for many vaccine-type serotypes. However, serotype 3 (SPN3) continues to cause significant disease and is identified in colonisation epidemiological studies as one of the top circulating serotypes in adults in the UK. Consequently, new vaccines that provide greater protection against SPN3 colonisation/carriage are urgently needed. The Experimental Human Pneumococcal Challenge (EHPC) model is a unique method of determining pneumococcal colonisation rates, understanding acquired immunity, and testing vaccines in a cost-effective manner. To enhance the development of effective pneumococcal vaccines against SPN3, we aim to develop a new relevant and safe SPN3 EHPC model with high attack rates which could be used to test vaccines using small sample size. This is a human challenge study to establish a new SPN3 EHPC model, consisting of two parts. In the dose-ranging/safety study, cohorts of 10 healthy participants will be challenged with escalating doses of SPN3. If first challenge does not lead into colonisation, participants will receive a second challenge 2 weeks after. Experimental nasopharyngeal (NP) colonisation will be determined using nasal wash sampling. Using the dose that results in ≥50% of participants being colonised, with a high safety profile, we will complete the cohort with another 33 participants to check for reproducibility of the colonisation rate. The primary outcome of this study is to determine the optimal SPN3 dose and inoculation regime to establish the highest rates of NP colonisation in healthy adults. Secondary outcomes include determining density and duration of experimental SPN3 NP colonisation and characterising mucosal and systemic immune responses to SPN3 challenge. This study is approved by the NHS Research and Ethics Committee (reference 22/NW/0051). Findings will be published in peer-reviewed journals and reports will be made available to participants.

Identifiants

pubmed: 38199622
pii: bmjopen-2023-075948
doi: 10.1136/bmjopen-2023-075948
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e075948

Informations de copyright

© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Phoebe Hazenberg (P)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.

Ryan E Robinson (RE)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Respiratory Department, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.

Madlen Farrar (M)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.

Carla Solorzano (C)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Oxford Vaccine Group, University of Oxford, Oxford, UK.

Angela Hyder-Wright (A)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Respiratory Department, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.

Konstantinos Liatsikos (K)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.

Jaye Brunning (J)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.

Hannah Fleet (H)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.

Amy Bettam (A)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.

Ashleigh Howard (A)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.

Tinashe Kenny-Nyazika (T)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.

Britta Urban (B)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Oxford Vaccine Group, University of Oxford, Oxford, UK.

Elena Mitsi (E)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Oxford Vaccine Group, University of Oxford, Oxford, UK.

Dima El Safadi (D)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.

Kelly Davies (K)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.

Maia Lesosky (M)

Global Health Trials Unit, Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.

Stephen B Gordon (SB)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.

Daniela M Ferreira (DM)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Oxford Vaccine Group, University of Oxford, Oxford, UK.

Andrea M Collins (AM)

Liverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK Andrea.collins@lstmed.ac.uk.
Respiratory Department, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.

Classifications MeSH