Evidence map›Paper›PMID 38199622›Full record

ArticleBMJ open2024

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

Phoebe Hazenberg, Ryan E Robinson, Madlen Farrar, Carla Solorzano, Angela Hyder-Wright, Konstantinos Liatsikos, Jaye Brunning, Hannah Fleet, Amy Bettam, Ashleigh Howard and 9 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in BMJ open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05535868 (Serotype 3 Experimental Human Pneumococcal Challenge; Dose Ranging and Reproducibility in a Healthy Volunteer Population), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.7field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05535868 nacompletednot on this map

Serotype 3 Experimental Human Pneumococcal Challenge; Dose Ranging and Reproducibility in a Healthy Volunteer Population

TypeinterventionalSponsorLiverpool School of Tropical MedicineRan2022 to 2023Enrolled91ConditionsStreptococcus Pneumonia, Controlled Human InfectionArmsSerotype 3 Experimental Human Pneumococcal Challenge - Liverpool Isolate (LIV014-S3), Serotype 3 Experimental Human Pneumococcal Challenge - Malawi Isolate (MLW-10V)
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 2 institutions in 2 countries.

Phoebe HazenbergLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.ORCID 0000-0002-0356-8959
Ryan E RobinsonLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Madlen FarrarLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Carla SolorzanoLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Angela Hyder-WrightLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Konstantinos LiatsikosLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Jaye BrunningLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Hannah FleetLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Amy BettamLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Ashleigh HowardLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Tinashe Kenny-NyazikaLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Britta UrbanLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Elena MitsiLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Dima El SafadiLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Kelly DaviesLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Maia LesoskyGlobal Health Trials Unit, Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Stephen B GordonLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Daniela M FerreiraLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK.
Andrea M CollinsLiverpool Vaccine Group, Liverpool School of Tropical Medicine, Liverpool, UK Andrea.collins@lstmed.ac.uk.
Liverpool School of Tropical Medicine · GBUniversity of Liverpool · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSince 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. METHODS AND ANALYSIS: 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. ETHICS AND DISSEMINATION: 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.

Indexed as

Adaptive ImmunityPneumococcal VaccinesAdultHealthy VolunteersHumansReproducibility of ResultsSerogroupStreptococcus pneumoniaePneumococcal VaccinesAdult thoracic medicineBACTERIOLOGYClinical TrialImmunologyRespiratory infections

Identifiers

PMID38199622
PMCPMC10806732
OpenAlexW4390706016

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.