Evidence map›Paper›PMID 32070679›Full record

Trial reportVaccine2020

Use of traditional serological methods and oral fluids to assess immunogenicity in children aged 2-16 years after successive annual vaccinations with LAIV.

Katja Hoschler, Sunil Maharjan, Heather Whitaker, Jo Southern, Blessing Okai, Janice Baldevarona, Paul J Turner, Nick J Andrews, Elizabeth Miller, Maria Zambon

Open access · hybridAbstract readClinical Trial, Phase IIIClinical Trial, Phase IVMulticenter Study
In one paragraph

Trial report in Vaccine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 26% 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.

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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
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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

10 authors at 1 institution in 1 country.

Katja HoschlerVirus Reference Department, Public Health England (Colindale), London, UK. Electronic address: katja.hoschler@phe.gov.uk.
Sunil MaharjanVirus Reference Department, Public Health England (Colindale), London, UK.
Heather WhitakerStatistics, Modelling and Economics Department, Public Health England (Colindale), London, UK.
Jo SouthernImmunisation and Countermeasures, Public Health England (Colindale), London, UK.
Blessing OkaiVirus Reference Department, Public Health England (Colindale), London, UK.
Janice BaldevaronaVirus Reference Department, Public Health England (Colindale), London, UK.
Paul J TurnerImmunisation and Countermeasures, Public Health England (Colindale), London, UK; National Heart and Lung Institute, Imperial College London, UK.
Nick J AndrewsStatistics, Modelling and Economics Department, Public Health England (Colindale), London, UK.
Elizabeth MillerImmunisation and Countermeasures, Public Health England (Colindale), London, UK.
Maria ZambonVirus Reference Department, Public Health England (Colindale), London, UK.
Public Health England · GB

Funding

Medical Research Council MR/K010468/1
6 · The paper itself

Abstract

backgroundThe UK introduced quadrivalent live attenuated influenza vaccine (qLAIV) for children in 2013/2014. The impact of annual vaccination on effectiveness and immunogenicity is being assessed.

methodA phase III/IV open-label study of the immunogenicity of annual vaccination with qLAIV (Fluenz™) was conducted over three consecutive years (2014/15-2016/17) in 254, 249 and 162 children respectively. Serum responses to vaccine components were measured by Haemagglutination Inhibition (HAI) and anti-A(H1N1)pdm09 Neuraminidase (NAI) assays, stratified according to previous receipt of AS03

findingsMore paired pre- and post-vaccination oral fluids (96%) than paired sera (87%) were obtained. Geometric mean titre rises using HAI assays were limited, with maximum rises seen in year one for both influenza B strains when 39% and 43% of subjects seroconverted (95% confidence interval 33-46% and 36-50%, respectively) and year two for influenza H3N2, when 40% (33-46%) individuals seroconverted. Prior pandemic vaccine receipt resulted in higher pre- and post-vaccination A(H1N1)pdm09 HAI titres and lower pre-and post-vaccination NAI (N1 neuraminidase) titres in all three years. OF results were congruent with HAI results; assay specificity compared to HAI was 88.1 and 71.6 percent, and sensitivity was 86.4 and 74.8 percent respectively for A(H1N1)pdm09 and H3N2.

conclusionIn all three study years, vaccination with qLAIV resulted in poor antibody responses. However, OFs are an alternative specimen type that allows self sampling, can easily be obtained from children, and their analysis leads to similar conclusions as classic serology by HAI. Their suitability for seroprevalence studies should be investigated. We demonstrated a sustained effect from prior receipt of the AS03

Indexed as

AdolescentAntibodies, ViralChildChild, PreschoolFemaleHumansImmunization ScheduleInfluenza A Virus, H1N1 SubtypeInfluenza A Virus, H3N2 SubtypeInfluenza, HumanInfluenza VaccinesMaleSalivaUnited KingdomVaccinationVaccines, AttenuatedAntibodies, ViralInfluenza VaccinesVaccines, AttenuatedImmunogenicityInfluenzaOil-in-water adjuvantOral fluidVaccine

Identifiers

PMID32070679
PMCPMC7054836
OpenAlexW3006062203

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.