Protocol for a phase IV double-blind randomised controlled trial to investigate the effect of the 13-valent pneumococcal conjugate vaccine and the 23-valent pneumococcal polysaccharide vaccine on pneumococcal colonisation using the experimental human pneumococcal challenge model in healthy adults (PREVENTING PNEUMO 2).


Journal

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

Informations de publication

Date de publication:
07 07 2022
Historique:
entrez: 7 7 2022
pubmed: 8 7 2022
medline: 12 7 2022
Statut: epublish

Résumé

Despite widely available vaccinations Healthy adult participants aged 18-50 years will be randomised to receive PCV13, PPV23 or placebo and then undergo one or two EHPCs involving intranasal administration of SPN at 1-month post-vaccination with serotype 3 (SPN3) and 6 months with serotype 6B (SPN6B). Participants randomised to PCV13 and placebo will also be randomised to one of two clinically relevant SPN3 strains from distinct lineages within clonal complex 180, clades Ia and II, creating five study groups. Following inoculation, participants will be seen on days 2, 7, 14 and 23. During the follow-up period, we will monitor safety, colonisation status, density and duration, immune responses and antigenuria. The primary outcome of the study is comparing the rate of SPN3 acquisition between the vaccinated (PCV13 or PPV23) and unvaccinated (placebo) groups as defined by classical culture. Density and duration of colonisation, comparison of acquisition rates using molecular methods and evaluation of the above measurements for individual SPN3 clades and SPN6B form the secondary objectives. Furthermore, we will explore the immune responses associated with these vaccines, their effect on colonisation and the relationship between colonisation and urinary pneumococcal antigen detection. The study is approved by the NHS Research and Ethics Committee (Reference: 20/NW/0097) and by the Medicines and Healthcare products Regulatory Agency (Reference: CTA 25753/0001/001-0001). Findings will be published in peer-reviewed journals. ISRCTN15728847, NCT04974294.

Identifiants

pubmed: 35798520
pii: bmjopen-2022-062109
doi: 10.1136/bmjopen-2022-062109
pmc: PMC9263934
doi:

Substances chimiques

Pneumococcal Vaccines 0
Vaccines, Conjugate 0

Banques de données

ClinicalTrials.gov
['NCT04974294']

Types de publication

Clinical Trial Protocol Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e062109

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR002535
Pays : United States

Investigateurs

Kelly Convey (K)
James Court (J)
Madlen Farrar (M)
Fred Fyles (F)
Josh Hamilton (J)
Phoebe Hazenberg (P)
Helen Hill (H)
Lisa Hitchins (L)
Ashleigh Howard (A)
Tinashe K Nyazika (TK)
Lauren Kerruish (L)
Samuel Latham (S)
Annabel Murphy (A)
Elissavet Nikolaou (E)
Angelina Peterson (A)
Hassan Burhan (H)
Ben Morton (B)

Informations de copyright

© Author(s) (or their employer(s)) 2022. 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: The study has received funding from Pfizer, which manufactures PCV13. Collaborators from Pfizer had direct input in the study design. AQ, CT, EB, KP, ASA and BDG are employees of Pfizer, and may own Pfizer stock.

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Auteurs

Konstantinos Liatsikos (K)

Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.

Angela Hyder-Wright (A)

Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Respiratory Research Group, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.

Sherin Pojar (S)

Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.

Tao Chen (T)

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

Duolao Wang (D)

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

Kelly Davies (K)

Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.

Christopher Myerscough (C)

Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.

Jesus Reine (J)

Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.

Ryan E Robinson (RE)

Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Respiratory Research Group, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.

Britta Urban (B)

Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.

Elena Mitsi (E)

Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.

Carla Solorzano (C)

Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.

Stephen B Gordon (SB)

Malawi Liverpool Wellcome Trust Clinical Research Programme, Liverpool School of Tropical Medicine, Blantyre, Malawi.

Angela Quinn (A)

Pfizer Vaccines, Pfizer Inc, Collegeville, Pennsylvania, USA.

Kaijie Pan (K)

Pfizer Vaccines, Pfizer Inc, Collegeville, Pennsylvania, USA.

Annaliesa S Anderson (AS)

Vaccines Research and Development, Pfizer Inc, Pearl River, New York, USA.

Christian Theilacker (C)

Pfizer Vaccines, Pfizer Inc, Collegeville, Pennsylvania, USA.

Elizabeth Begier (E)

Pfizer Vaccines, Pfizer Inc, Collegeville, Pennsylvania, USA.

Bradford D Gessner (BD)

Pfizer Vaccines, Pfizer Inc, Collegeville, Pennsylvania, USA.

Andrea Collins (A)

Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Respiratory Research Group, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.

Daniela M Ferreira (DM)

Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK Daniela.Ferreira@lstmed.ac.uk.

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