Journal article
Protocol for a phase IV, Experimental Human Pneumococcal Challenge (EHPC) model to investigate <i>Streptococcus pneumoniae</i> serotype 3 (SPN3) colonisation following PCV15, a double-blind randomised controlled trial in healthy participants aged 18-50 years in the UK (RATIONALE-15)
- Abstract:
- IntroductionStreptococcus pneumoniae serotype 3 (SPN3) remains a significant contributor to invasive pneumococcal disease globally, despite its inclusion in widely administered vaccines. The next generation of pneumococcal vaccines may confer better protection against this serotype, reducing disease burden. We describe an ethically approved protocol for a double-blind randomised controlled trial assessing the impact of VAXNEUVANCE (15-valent pneumococcal conjugated vaccine (PCV15)) and 0.9% saline (placebo) on the acquisition, density and duration of SPN3 carriage using a controlled human infection model.Methods and analysisHealthy adults aged 18-50 years will be randomised 1:1 to receive PCV15 or placebo. Participants will be considered enrolled on the trial at vaccination. One month following vaccination, all participants will be intranasally inoculated with SPN3. Following inoculation, participants will be followed up on days 2, 7, 14 and 28 to monitor safety, SPN3 colonisation status, density and duration, as well as immune responses. The primary endpoint of the study is to assess the rate of SPN3 acquisition between vaccinated and unvaccinated participants defined by classical microbiological methods. Secondary endpoints will determine the density and duration of SPN3 colonisation and compare the immune responses between study groups. An exploratory cohort of 5 participants will be asked to consent to a nasal biopsy procedure during a screening visit and a second nasal biopsy 28 days after PCV15 vaccination. This cohort will only receive PCV15 and will not be challenged. Through this exploratory cohort, we will explore gene expression changes induced by PCV15 vaccination and their visualisation (spatial location) within the nasal tissue.Ethics and disseminationThis protocol has been reviewed by the sponsor, funder and external peer reviewers. The study is approved by the NHS Research and Ethics Committee (Reference: 24/SC/0388) and by the Medicines and Healthcare Products Regulatory Agency (Reference: CTA 21584/0485/001-0001).Trial registration numberNCT06731374 - ISRCTN91656864.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 618.2KB, Terms of use)
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- Publisher copy:
- 10.1136/bmjopen-2025-106028
Authors
- Publisher:
- BMJ Publishing Group
- Journal:
- BMJ Open More from this journal
- Volume:
- 15
- Issue:
- 11
- Pages:
- e106028
- Publication date:
- 2025-11-24
- Acceptance date:
- 2025-11-03
- DOI:
- EISSN:
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2044-6055
- ISSN:
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2044-6055
- Pmid:
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41290307
- Language:
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English
- Keywords:
-
- Pubs id:
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2338179
- UUID:
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uuid_d7d2b557-34e6-4e1b-a0ac-24a0f416fa58
- Local pid:
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pubs:2338179
- Source identifiers:
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3532607
- Deposit date:
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2025-12-04
- ARK identifier:
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- Copyright date:
- 2025
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