Evidence map›Paper›PMID 33314126›Full record

Trial reportClinical and experimental immunology2021

Pre-existing influenza-specific nasal IgA or nasal viral infection does not affect live attenuated influenza vaccine immunogenicity in children.

M E Cole, R Kundu, A F Abdulla, N Andrews, K Hoschler, J Southern, D Jackson, E Miller, M Zambon, P J Turner and 1 more

Open access · bronzeAbstract readClinical Trial, Phase IV
In one paragraph

Trial report in Clinical and experimental immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Observational
  6. Mucosal vaccines - fortifying the frontiers.Nature reviews. Immunology · 2022
    Review
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

11 authors at 3 institutions in 1 country.

M E ColeDepartment of Infectious Disease, Imperial College London (St Mary's Campus), London, UK.
R KunduHealth Protection Research Unit in Respiratory Infections, Imperial College London, London, UK.
A F AbdullaDepartment of Infectious Disease, Imperial College London (St Mary's Campus), London, UK.
N AndrewsPublic Health England (Colindale), London, UK.
K HoschlerPublic Health England (Colindale), London, UK.
J SouthernPublic Health England (Colindale), London, UK.
D JacksonPublic Health England (Colindale), London, UK.
E MillerPublic Health England (Colindale), London, UK.
M ZambonPublic Health England (Colindale), London, UK.ORCID 0000-0002-8897-7881
P J TurnerHealth Protection Research Unit in Respiratory Infections, Imperial College London, London, UK.ORCID 0000-0001-9862-5161
J S TregoningDepartment of Infectious Disease, Imperial College London (St Mary's Campus), London, UK.ORCID 0000-0001-8093-8741
Public Health England · GBImperial College London · GBThe Pirbright Institute · GB

Funding

Medical Research Council MR/R021643/1National Institute for Health Research Imperial Biomedical Research Centre (BRC)National Institute for Health Research National Vaccine Evaluation Consortium
6 · The paper itself

Abstract

The United Kingdom has a national immunization programme which includes annual influenza vaccination in school-aged children, using live attenuated influenza vaccine (LAIV). LAIV is given annually, and it is unclear whether repeat administration can affect immunogenicity. Because LAIV is delivered intranasally, pre-existing local antibody might be important. In this study, we analysed banked samples from a study performed during the 2017/18 influenza season to investigate the role of pre-existing influenza-specific nasal immunoglobulin (Ig)A in children aged 6-14 years. Nasopharyngeal swabs were collected prior to LAIV immunization to measure pre-existing IgA levels and test for concurrent upper respiratory tract viral infections (URTI). Oral fluid samples were taken at baseline and 21-28 days after LAIV to measure IgG as a surrogate of immunogenicity. Antibody levels at baseline were compared with a pre-existing data set of LAIV shedding from the same individuals, measured by reverse transcription-polymerase chain reaction. There was detectable nasal IgA specific to all four strains in the vaccine at baseline. However, baseline nasal IgA did not correlate with the fold change in IgG response to the vaccine. Baseline nasal IgA also did not have an impact upon whether vaccine virus RNA was detectable after immunization. There was no difference in fold change of antibody between individuals with and without an URTI at the time of immunization. Overall, we observed no effect of pre-existing influenza-specific nasal antibody levels on immunogenicity, supporting annual immunization with LAIV in children.

Indexed as

Administration, IntranasalAdolescentAntibodies, ViralChildFemaleHumansImmunogenicity, VaccineImmunoglobulin AImmunoglobulin GInfluenza A Virus, H1N1 SubtypeInfluenza A Virus, H3N2 SubtypeInfluenza, HumanInfluenza VaccinesMaleNasal CavityVaccinationAntibodies, ViralImmunoglobulin AImmunoglobulin GInfluenza VaccinesVaccines, AttenuatedIgAinfluenzaLAIVmucosalschoolchildren

Identifiers

PMID33314126
PMCPMC7944357
OpenAlexW3113317969

What OpenQuestion holds

Textmetadata
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.