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).
Epidemiology
Immunology
PREVENTIVE MEDICINE
Public health
Respiratory infections
Journal
BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874
Informations de publication
Date de publication:
07 07 2022
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
e062109Subventions
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.
Références
Clin Infect Dis. 2019 May 30;68(12):2135-2143
pubmed: 30357326
Infect Dis Ther. 2021 Mar;10(1):521-539
pubmed: 33587245
PLoS Pathog. 2012;8(4):e1002622
pubmed: 22496648
mBio. 2021 Jan 12;12(1):
pubmed: 33436429
Vaccine. 2016 Mar 18;34(13):1496-1503
pubmed: 26899376
Epidemiol Infect. 2005 Oct;133(5):891-8
pubmed: 16181510
J Infect Dis. 2005 Aug 1;192(3):387-93
pubmed: 15995951
Microorganisms. 2022 Mar 04;10(3):
pubmed: 35336135
Lancet Infect Dis. 2018 Oct;18(10):e312-e322
pubmed: 29891332
Genes (Basel). 2019 Oct 25;10(11):
pubmed: 31731573
Am J Respir Crit Care Med. 2013 Apr 15;187(8):855-64
pubmed: 23370916
Vaccine. 2019 Jul 9;37(30):4147-4154
pubmed: 31155413
J Biomed Inform. 2009 Apr;42(2):377-81
pubmed: 18929686
Clin Infect Dis. 2021 Aug 16;73(4):650-658
pubmed: 33507250
Vaccine. 2019 Jul 9;37(30):3953-3956
pubmed: 31176540
Wkly Epidemiol Rec. 2008 Oct 17;83(42):373-84
pubmed: 18927997
Am J Respir Crit Care Med. 2015 Oct 1;192(7):853-8
pubmed: 26114410
Vaccine. 2019 Sep 10;37(38):5777-5787
pubmed: 29861177
PLoS One. 2017 Jan 6;12(1):e0169368
pubmed: 28061505
Clin Infect Dis. 2020 Nov 5;71(8):e235-e243
pubmed: 31955196
Lancet Infect Dis. 2018 Apr;18(4):441-451
pubmed: 29395999
Clin Vaccine Immunol. 2015 Dec 16;23(2):162-7
pubmed: 26677201
PLoS One. 2020 Mar 10;15(3):e0229558
pubmed: 32155176
N Engl J Med. 2015 Mar 19;372(12):1114-25
pubmed: 25785969
Vaccine. 2016 Mar 18;34(13):1540-1550
pubmed: 26899372
Vaccine. 2016 Jan 2;34(1):4-6
pubmed: 26602269
PLoS One. 2021 Feb 4;16(2):e0246522
pubmed: 33539406
Clin Infect Dis. 2021 Dec 30;:
pubmed: 34967907
Eur Respir J. 2013 Nov;42(5):1283-90
pubmed: 23397295
Am J Respir Crit Care Med. 2021 Mar 1;203(5):604-613
pubmed: 32941735
PLoS Pathog. 2018 Nov 26;14(11):e1007438
pubmed: 30475919
J Vis Exp. 2013 Feb 15;(72):
pubmed: 23439027
BMJ. 2013 Jan 08;346:e7586
pubmed: 23303884
Front Cell Infect Microbiol. 2020 Dec 23;10:613287
pubmed: 33425786
MMWR Morb Mortal Wkly Rep. 2019 Nov 22;68(46):1069-1075
pubmed: 31751323
Expert Rev Vaccines. 2020 Apr;19(4):353-366
pubmed: 32237926
J Biomed Inform. 2019 Jul;95:103208
pubmed: 31078660
J Infect Dis. 2021 May 20;223(9):1590-1600
pubmed: 32877517
Microorganisms. 2022 May 12;10(5):
pubmed: 35630521
Am J Respir Crit Care Med. 2016 Dec 15;194(12):1523-1531
pubmed: 27403678
Clin Infect Dis. 2018 Jun 18;67(1):42-49
pubmed: 29324986
Clin Microbiol Infect. 2014 Dec;20(12):O1145-51
pubmed: 24995531
Cochrane Database Syst Rev. 2013 Jan 31;(1):CD000422
pubmed: 23440780
Trends Microbiol. 2011 Sep;19(9):464-70
pubmed: 21784641
Clin Infect Dis. 2013 Oct;57(7):952-62
pubmed: 23804191