Evidence map›Paper›PMID 37141259›Full record

SynthesisPloS one2023

Comprehensive review of safety in Experimental Human Pneumococcal Challenge.

Ryan E Robinson, Christopher Myerscough, Nengjie He, Helen Hill, Wendi A Shepherd, Patricia Gonzalez-Dias, Konstantinos Liatsikos, Samuel Latham, Fred Fyles, Klara Doherty and 15 more

Abstract readReviewMeta-Analysis
In one paragraph

Synthesis in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. 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

25 authors.

Ryan E RobinsonClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.ORCID 0000-0003-0871-4780
Christopher MyerscoughClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Nengjie HeClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Helen HillClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Wendi A ShepherdNorth West Health Protection Team, UK Health Security Agency, Liverpool, United Kingdom.ORCID 0000-0001-9142-0219
Patricia Gonzalez-DiasClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.ORCID 0000-0002-6434-3841
Konstantinos LiatsikosClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Samuel LathamClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.ORCID 0000-0003-2186-4652
Fred FylesClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.ORCID 0000-0002-5141-6220
Klara DohertyClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Phoebe HazenbergClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Fathimath ShihamClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Daniella MclenghanClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Hugh AdlerClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Vicki RandlesClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Seher ZaidiClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Angela Hyder-WrightClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Elena MitsiClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Hassan BurhanClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Ben MortonClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.ORCID 0000-0002-6164-2854
Jamie RylanceClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Maia LesoskyClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.ORCID 0000-0002-2026-958X
Stephen B GordonClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.ORCID 0000-0001-6576-1116
Andrea M CollinsClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Daniela M FerreiraClinical Sciences Department, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionExperimental Human Pneumococcal Challenge (EHPC) involves the controlled exposure of adults to a specific antibiotic-sensitive Streptococcus pneumoniae serotype, to induce nasopharyngeal colonisation for the purpose of vaccine research. The aims are to review comprehensively the safety profile of EHPC, explore the association between pneumococcal colonisation and frequency of safety review and describe the medical intervention required to undertake such studies.

methodsA single-centre review of all EHPC studies performed 2011-2021. All recorded serious adverse events (SAE) in eligible studies are reported. An unblinded meta-analysis of collated anonymised individual patient data from eligible EHPC studies was undertaken to assess the association between experimental pneumococcal colonisation and the frequency of safety events following inoculation.

resultsIn 1416 individuals (median age 21, IQR 20-25), 1663 experimental pneumococcal inoculations were performed. No pneumococcal-related SAE have occurred. 214 safety review events were identified with 182 (12.85%) participants presenting with symptoms potentially in keeping with pneumococcal infection, predominantly in pneumococcal colonised individuals (colonised = 96/658, non-colonised = 86/1005, OR 1.81 (95% CI 1.28-2.56, P = <0.001). The majority were mild (pneumococcal group = 72.7% [120/165 reported symptoms], non-pneumococcal = 86.7% [124/143 reported symptoms]). 1.6% (23/1416) required antibiotics for safety. DISCUSSION: No SAEs were identified directly relating to pneumococcal inoculation. Safety review for symptoms was infrequent but occurred more in experimentally colonised participants. Most symptoms were mild and resolved with conservative management. A small minority required antibiotics, notably those serotype 3 inoculated.

conclusionOutpatient human pneumococcal challenge can be conducted safely with appropriate levels of safety monitoring procedures in place.

Indexed as

Pneumococcal InfectionsStreptococcus pneumoniaeAdultAnti-Bacterial AgentsHumansNasopharynxPneumococcal VaccinesYoung AdultAnti-Bacterial AgentsPneumococcal Vaccines

Identifiers

PMID37141259
PMCPMC10159102

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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 OpenQuestion graph.